Variant #0000550608 (NC_000013.10:g.32945108T>C, NM_000059.3:c.8503T>C (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.32945108T>C
DNA change (hg38) g.32370971T>C
Published as BRCA2(NM_000059.3):c.8503T>C (p.S2835P, p.(Ser2835Pro)), BRCA2(NM_000059.4):c.8503T>C (p.S2835P)
ISCN -
DB-ID BRCA2_000338 See all 18 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) 0.00056 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 2019-07-18 18:22:55 +02:00 (CEST)
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.8503T>C r.(?) p.(Ser2835Pro) -


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