Variant #0000271989 (NC_000013.10:g.32914814C>T, NM_000059.3:c.6322C>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32914814C>T
DNA change (hg38) g.32340677C>T
Published as BRCA2(NM_000059.3):c.6322C>T (p.R2108C, p.(Arg2108Cys)), BRCA2(NM_000059.4):c.6322C>T (p.R2108C)
ISCN -
DB-ID BRCA2_000508 See all 41 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) 0.00059 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +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.6322C>T r.(?) p.(Arg2108Cys) -


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