Variant #0000978825 (NC_000009.11:g.98011545C>T, NM_000136.2:c.29G>A (FANCC))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.98011545C>T
DNA change (hg38) -
Published as FANCC(NM_000136.2):c.29G>A (p.C10Y), FANCC(NM_000136.3):c.29G>A (p.(Cys10Tyr))
ISCN -
DB-ID FANCC_000084 See all 4 reported entries
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) 0.0005 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCC NM_000136.2 ?/. - c.29G>A r.(?) p.(Cys10Tyr) -


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