Variant #0000861765 (NC_000009.11:g.98011509del, NM_000136.2:c.67del (FANCC))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.98011509del
DNA change (hg38) -
Published as FANCC(NM_000136.2):c.67delG (p.(Asp23Ilefs*23)), FANCC(NM_000136.2):c.67delG (p.D23Ifs*23), FANCC(NM_000136.3):c.67delG (p.D23Ifs*23)
ISCN -
DB-ID FANCC_000006 See all 67 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCC NM_000136.2 +/. - c.67del r.(?) p.(Asp23IlefsTer23) -


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