Variant #0000723377 (NC_000011.9:g.22646532C>T, NM_022725.3:c.825G>A (FANCF))

Chromosome 11
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.22646532C>T
DNA change (hg38) -
Published as FANCF(NM_022725.3):c.825G>A (p.(Leu275=), p.L275=), FANCF(NM_022725.4):c.825G>A (p.L275=)
ISCN -
DB-ID FANCF_000012 See all 5 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) 0.01845 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCF NM_022725.3 -/. - c.825G>A r.(?) p.(Leu275=) -


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