Variant #0000559984 (NC_000016.9:g.89842176C>G, NM_000135.2:c.1874G>C (FANCA))

Chromosome 16
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.89842176C>G
DNA change (hg38) g.89775768C>G
Published as FANCA(NM_000135.4):c.1874G>C (p.C625S), FANCA(NM_001286167.2):c.1874G>C (p.C625S)
ISCN -
DB-ID FANCA_000554 See all 6 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) 0.00238 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCA NM_000135.2 ?/. - c.1874G>C r.(?) p.(Cys625Ser) -
ZNF276 NM_152287.3 ?/. - c.*37522C>G r.(=) p.(=) -


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