Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Molecular Consequence: missense variant
(GRCh38)X:130133383C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130133383C>T
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, splice_donor_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133383C>T
(GRCh38)X:130136652G>A
(Homo sapiens)Allele/Variant
Source: rs2030352383
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136652G>A
(GRCh38)X:130136687C>T
(Homo sapiens)Allele/Variant
Source: rs1057521792
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136687C>T
(GRCh38)X:130129579A>T
(Homo sapiens)Allele/Variant
Source: rs863223899
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129579A>T
(GRCh38)X:130149545A>G
(Homo sapiens)Allele/Variant
Source: rs1139851
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130149545A>G
(GRCh38)X:130149560C>A
(Homo sapiens)Allele/Variant
Source: rs376209388
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130149560C>A
(GRCh38)X:130130061T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130130061T>C
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130061T>C
(GRCh38)X:130130161C>T
(Homo sapiens)Allele/Variant
Source: rs2030006759
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130161C>T
(GRCh38)X:130137147C>T
(Homo sapiens)Allele/Variant
Source: rs1603223158
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130137147C>T
(GRCh38)X:130130110G>A
(Homo sapiens)Allele/Variant
Source: rs752745547
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130110G>A
(GRCh38)X:130130000G>A
(Homo sapiens)Allele/Variant
Source: rs1455517770
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130000G>A
(GRCh38)X:130130045G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130130045G>A
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130045G>A
(GRCh38)X:130133352G>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130133352G>C
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133352G>C
(GRCh38)X:130130138T>C
(Homo sapiens)Allele/Variant
Source: rs2030004639
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130138T>C
(GRCh38)X:130133412C>T
(Homo sapiens)Allele/Variant
Source: rs1424829478
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133412C>T
(GRCh38)X:130129620C>T
(Homo sapiens)Allele/Variant
Source: rs200543681
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129620C>T
(GRCh38)X:130147610G>C
(Homo sapiens)Allele/Variant
Source: rs1313521061
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130147610G>C
(GRCh38)X:130147766C>T
(Homo sapiens)Allele/Variant
Source: rs999882329
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130147766C>T
(GRCh38)X:130138594C>T
(Homo sapiens)Allele/Variant
Source: rs762443189
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130138594C>T
(GRCh38)X:130147546G>A
(Homo sapiens)Allele/Variant
Source: rs762588571
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130147546G>A
(mRatBN7.2)X:127650857C>A
(Rattus norvegicus)Allele/Variant
Source: rs8151193
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127650857C>A
(GRCm39)X:47573461T>C
(Mus musculus)Allele/Variant
Source: rs249424331
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)X:47573461T>C
(GRCm39)X:47564579G>C
(Mus musculus)Allele/Variant
Source: rs231159669
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)X:47564579G>C
(GRCm39)X:47564586T>G
(Mus musculus)Allele/Variant
Source: rs250721002
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)X:47564586T>G
(GRCh38)X:130137080C>T
(Homo sapiens)Allele/Variant
Source: rs1043351232
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130137080C>T
(GRCh38)X:130138679T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130138679T>C
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130138679T>C
(GRCh38)X:130137152A>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130137152A>T
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130137152A>T
(GRCh38)X:130130113T>C
(Homo sapiens)Allele/Variant
Source: rs1175521163
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130113T>C
(GRCh38)X:130130186C>A
(Homo sapiens)Allele/Variant
Source: rs749868550
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130186C>A
(GRCh38)X:130138600G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130138600G>A
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130138600G>A
(GRCh38)X:130136165C>G
(Homo sapiens)Allele/Variant
Source: rs2124651866
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136165C>G
(GRCh38)X:130136169A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130136169A>G
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136169A>G
(GRCh38)X:130136693C>T
(Homo sapiens)Allele/Variant
Source: rs1056740593
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136693C>T
(GRCh38)X:130129626G>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130129626G>C
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129626G>C
(GRCh38)X:130130066C>G
(Homo sapiens)Allele/Variant
Source: rs1391324425
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130066C>G
(GRCh38)X:130130078G>A
(Homo sapiens)Allele/Variant
Source: rs2029999691
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130078G>A
(GRCh38)X:130133424T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130133424T>C
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133424T>C
(GRCh38)X:130136110T>C
(Homo sapiens)Allele/Variant
Source: rs2124651762
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136110T>C
(GRCh38)X:130136123A>C
(Homo sapiens)Allele/Variant
Source: rs61730898
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136123A>C
(GRCh38)X:130138685C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.130138685C>T
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130138685C>T
(GRCh38)X:130136695G>T
(Homo sapiens)Allele/Variant
Source: rs2030354409
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136695G>T
(GRCh38)X:130147792G>A
(Homo sapiens)Allele/Variant
Source: rs724160015
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130147792G>A
(GRCh38)X:130165649C>T
(Homo sapiens)Allele/Variant
Source: rs769299264
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130165649C>T
(GRCh38)X:130129989C>T
(Homo sapiens)Allele/Variant
Source: rs747871895
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129989C>T
(GRCh38)X:130130132G>A
(Homo sapiens)Allele/Variant
Source: rs193002766
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130132G>A
(GRCh38)X:130140604T>C
(Homo sapiens)Allele/Variant
Source: rs1202786652
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130140604T>C
(GRCh38)X:130138637C>T
(Homo sapiens)Allele/Variant
Source: rs1603224226
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130138637C>T
(GRCh38)X:130137525T>C
(Homo sapiens)Allele/Variant
Source: rs935187661
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130137525T>C
(GRCh38)X:130136185C>A
(Homo sapiens)Allele/Variant
Source: rs2124651900
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136185C>A
(GRCh38)X:130129616C>T
(Homo sapiens)Allele/Variant
Source: rs2124643483
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129616C>T