Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: RTCB (Hsa)
(GRCh38)22:32407123T>C
(Homo sapiens)Allele/Variant
Source: rs207477955
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32407123T>C
(GRCh38)22:32398033T>C
(Homo sapiens)Allele/Variant
Source: rs776896020
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32398033T>C
(GRCh38)22:32398100A>G
(Homo sapiens)Allele/Variant
Source: rs750059803
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32398100A>G
(GRCh38)22:32393947A>G
(Homo sapiens)Allele/Variant
Source: rs765879347
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32393947A>G
(GRCh38)22:32388040G>C
(Homo sapiens)Allele/Variant
Source: rs374100495
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32388040G>C
(GRCh38)22:32401757T>C
(Homo sapiens)Allele/Variant
Source: rs200793446
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32401757T>C
(GRCh38)22:32395208C>T
(Homo sapiens)Allele/Variant
Source: rs202229511
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395208C>T
(GRCh38)22:32396205T>C
(Homo sapiens)Allele/Variant
Source: rs113907276
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32396205T>C
(GRCh38)22:32395072G>A
(Homo sapiens)Allele/Variant
Source: rs1048524937
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395072G>A
(GRCh38)22:32399645G>A
(Homo sapiens)Allele/Variant
Source: rs267606232
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32399645G>A
(GRCh38)22:32395103G>A
(Homo sapiens)Allele/Variant
Source: rs1022695727
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395103G>A
(GRCh38)22:32399686C>G
(Homo sapiens)Allele/Variant
Source: rs1335962461
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32399686C>G
(GRCh38)22:32401866C>G
(Homo sapiens)Allele/Variant
Source: NC_000022.11:g.32401866C>G
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32401866C>G
(GRCh38)22:32395164C>G
(Homo sapiens)Allele/Variant
Source: rs41310258
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395164C>G
(GRCh38)22:32396088A>G
(Homo sapiens)Allele/Variant
Source: NC_000022.11:g.32396088A>G
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32396088A>G
(GRCh38)22:32395091C>T
(Homo sapiens)Allele/Variant
Source: NC_000022.11:g.32395091C>T
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395091C>T
(GRCh38)22:32399623T>C
(Homo sapiens)Allele/Variant
Source: NC_000022.11:g.32399623T>C
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32399623T>C
(GRCh38)22:32395172G>T
(Homo sapiens)Allele/Variant
Source: rs912443635
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395172G>T
(GRCh38)22:32396165G>A
(Homo sapiens)Allele/Variant
Source: rs1933242631
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32396165G>A
(GRCh38)22:32408757C>T
(Homo sapiens)Allele/Variant
Source: NC_000022.11:g.32408757C>T
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32408757C>T
(GRCh38)22:32392286A>G
(Homo sapiens)Allele/Variant
Source: rs145947916
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32392286A>G
(GRCh38)22:32396236A>G
(Homo sapiens)Allele/Variant
Source: rs10222228
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32396236A>G
(GRCh38)22:32395126T>C
(Homo sapiens)Allele/Variant
Source: rs141205917
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395126T>C