Variant #0000726090 (NC_000016.9:g.89828357C>T, NM_000135.2:c.2852G>A (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.89828357C>T
DNA change (hg38) -
Published as FANCA(NM_001286167.3):c.2852G>A (p.R951Q)
ISCN -
DB-ID FANCA_000412 See all 11 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.2852G>A r.(?) p.(Arg951Gln) -
ZNF276 NM_152287.3 +/. - c.*23703C>T r.(=) p.(=) -


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