Variant #0001002824 (NC_000016.9:g.89811369G>A, NM_000135.2:c.3624C>T (FANCA))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89811369G>A
DNA change (hg38) -
Published as FANCA(NM_000135.2):c.3624C>T (p.(Ser1208=)), FANCA(NM_000135.4):c.3624C>T (p.S1208=)
ISCN -
DB-ID FANCA_000444 See all 7 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) 0.00011 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCA NM_000135.2 +?/. - c.3624C>T r.(?) p.(=) -
VPS9D1 NM_004913.2 +?/. - c.-24100C>T r.(?) p.(=) -
ZNF276 NM_152287.3 +?/. - c.*6715G>A r.(=) p.(=) -


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