Variant #0001002838 (NC_000016.9:g.89865605C>A, NM_000135.2:c.862G>T (FANCA))

Chromosome 16
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.89865605C>A
DNA change (hg38) -
Published as FANCA(NM_000135.2):c.862G>T (p.(Glu288*)), FANCA(NM_000135.4):c.862G>T (p.E288*), FANCA(NM_001286167.2):c.862G>T (p.E288*)
ISCN -
DB-ID FANCA_000065 See all 19 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) 6.0E-5 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCA NM_000135.2 +/. - c.862G>T r.(?) p.(Glu288Ter) -
ZNF276 NM_152287.3 +/. - c.*60951C>A r.(=) p.(=) -


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