Variant #0000346696 (NC_000013.10:g.32972884A>G, NM_000059.3:c.10234A>G (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32972884A>G
DNA change (hg38) g.32398747A>G
Published as BRCA2(NM_000059.3):c.10234A>G (p.I3412V, p.(Ile3412Val)), BRCA2(NM_000059.4):c.10234A>G (p.I3412V)
ISCN -
DB-ID BRCA2_000485 See all 117 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) 0.02298 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 2018-01-15 20:58:59 +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.10234A>G r.(?) p.(Ile3412Val) -
N4BP2L1 NM_052818.2 -/- - c.*4195T>C r.(=) p.(=) -


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