Variant #0000337733 (NC_000013.10:g.32890726T>G, NC_000013.10(NM_000059.3):c.67+62T>G (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.32890726T>G
DNA change (hg38) g.32316589T>G
Published as BRCA2(NM_000059.3):c.67+62T>G
ISCN -
DB-ID BRCA2_000012 See all 7 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) Retrieve
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 2019-12-04 15:24:38 +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.67+62T>G r.(=) p.(=) -
ZAR1L NM_001136571.1 -?/. - c.-4664A>C r.(?) p.(=) -


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