Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Molecular Consequence: missense variant
(GRCh38)8:100142126G>A
(Homo sapiens)Allele/Variant
Source: rs754320394
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100142126G>A
(GRCh38)8:100140884C>A
(Homo sapiens)Allele/Variant
Source: rs954142586
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140884C>A
(GRCh38)8:100141572A>C
(Homo sapiens)Allele/Variant
Source: rs373258172
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141572A>C
(GRCh38)8:100134364C>T
(Homo sapiens)Allele/Variant
Source: rs373092371
Genes: FBXO43 (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)8:100134364C>T
(GRCh38)8:100141395C>T
(Homo sapiens)Allele/Variant
Source: rs1171227939
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141395C>T
(GRCh38)8:100133950C>T
(Homo sapiens)Allele/Variant
Source: rs370561864
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100133950C>T
(GRCh38)8:100137646A>T
(Homo sapiens)Allele/Variant
Source: rs759048586
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100137646A>T
(GRCh38)8:100141337A>G
(Homo sapiens)Allele/Variant
Source: rs376577612
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141337A>G
(GRCh38)8:100141707C>T
(Homo sapiens)Allele/Variant
Source: rs748362105
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141707C>T
(GRCh38)8:100133938C>T
(Homo sapiens)Allele/Variant
Source: rs954702094
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100133938C>T
(GRCh38)8:100140744T>C
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.100140744T>C
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140744T>C
(GRCh38)8:100140843C>T
(Homo sapiens)Allele/Variant
Source: rs1215477131
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140843C>T
(GRCh38)8:100140915G>A
(Homo sapiens)Allele/Variant
Source: rs373156415
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140915G>A
(GRCh38)8:100140986C>T
(Homo sapiens)Allele/Variant
Source: rs748943275
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140986C>T
(GRCh38)8:100141205T>C
(Homo sapiens)Allele/Variant
Source: rs530844525
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141205T>C
(GRCh38)8:100141209A>T
(Homo sapiens)Allele/Variant
Source: rs373910464
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141209A>T
(GRCh38)8:100141548C>T
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.100141548C>T
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141548C>T
(GRCh38)8:100145110C>A
(Homo sapiens)Allele/Variant
Source: rs1387007809
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100145110C>A
(GRCh38)8:100141935G>A
(Homo sapiens)Allele/Variant
Source: rs553559355
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141935G>A
(GRCh38)8:100141483A>C
(Homo sapiens)Allele/Variant
Source: rs369057548
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141483A>C
(GRCh38)8:100141567C>A
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.100141567C>A
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141567C>A
(GRCh38)8:100141848C>T
(Homo sapiens)Allele/Variant
Source: rs745750597
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141848C>T
(GRCh38)8:100141940T>C
(Homo sapiens)Allele/Variant
Source: rs1421611544
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141940T>C
(GRCh38)8:100140685G>C
(Homo sapiens)Allele/Variant
Source: rs201016433
Genes: FBXO43 (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)8:100140685G>C
(GRCh38)8:100133821C>T
(Homo sapiens)Allele/Variant
Source: rs202056051
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100133821C>T
(GRCh38)8:100140761A>G
(Homo sapiens)Allele/Variant
Source: rs267601676
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140761A>G
(GRCh38)8:100140976C>G
(Homo sapiens)Allele/Variant
Source: rs1223084666
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140976C>G
(GRCh38)8:100141949G>A
(Homo sapiens)Allele/Variant
Source: rs201306425
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141949G>A
(GRCm39)15:36163243G>A
(Mus musculus)Allele/Variant
Source: rs37196620
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36163243G>A
(GRCm39)15:36162119T>C
(Mus musculus)Allele/Variant
Source: rs36695570
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162119T>C
(GRCm39)15:36162613T>C
(Mus musculus)Allele/Variant
Source: rs36250616
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162613T>C
(GRCm39)15:36151897C>T
(Mus musculus)Allele/Variant
Source: rs261823030
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36151897C>T
(GRCm39)15:36162470T>C
(Mus musculus)Allele/Variant
Source: rs37137482
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162470T>C
(GRCm39)15:36162172T>G
(Mus musculus)Allele/Variant
Source: rs219055565
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162172T>G
(GRCm39)15:36162018A>C
(Mus musculus)Allele/Variant
Source: rs232921500
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162018A>C
(GRCm39)15:36164740G>A
(Mus musculus)Allele/Variant
Source: rs228471220
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36164740G>A
(GRCm39)15:36151854G>A
(Mus musculus)Allele/Variant
Source: rs233539226
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36151854G>A
(GRCm39)15:36162427T>C
(Mus musculus)Allele/Variant
Source: rs31846715
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162427T>C
(GRCm39)15:36162181A>G
(Mus musculus)Allele/Variant
Source: rs32017113
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162181A>G
(GRCm39)15:36162184G>A
(Mus musculus)Allele/Variant
Source: rs211723964
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36162184G>A