Variant #0001014537 (NC_000009.11:g.35077267G>A, NM_004629.1:c.640C>T (FANCG))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35077267G>A
DNA change (hg38) -
Published as FANCG(NM_004629.2):c.640C>T (p.R214C)
ISCN -
DB-ID FANCG_000085
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00067 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCG NM_004629.1 -/. - c.640C>T r.(?) p.(Arg214Cys) -
VCP NM_007126.3 -/. - c.-4917C>T r.(?) p.(=) -


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