Variant #0000623041 (NC_000013.10:g.32890587C>T, NM_000059.3:c.-11C>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.32890587C>T
DNA change (hg38) g.32316450C>T
Published as BRCA2(NM_000059.3):c.-11C>T, BRCA2(NM_000059.4):c.-11C>T
ISCN -
DB-ID BRCA2_000007 See all 12 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) 0.00112 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2019-12-06 12:43:26 +01:00 (CET)
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.-11C>T r.(?) p.(=) -
ZAR1L NM_001136571.1 -/. - c.-4525G>A r.(?) p.(=) -


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