Variant #0000679763 (NC_000013.10:g.32910430C>T, NM_000059.3:c.1938C>T (BRCA2))

Chromosome 13
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.32910430C>T
DNA change (hg38) -
Published as BRCA2(NM_000059.3):c.1938C>T (p.S646=, p.(Ser646=)), BRCA2(NM_000059.4):c.1938C>T (p.S646=)
ISCN -
DB-ID BRCA2_002001 See all 23 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) 0.001 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 -/. - c.1938C>T r.(?) p.(Ser646=) -


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