Full data view for gene BRCA2

Information The variants shown are described using the NM_000059.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     

Allele     

DNA change (genomic) (hg38)     

Published as     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Variant remarks     

Template     

Technique     

Disease     

Reference     

Gender     

Geographic origin     

Ethnic origin     

Population     

Remarks     

Microattribution     

Panel size     

Owner     
-/. 18 c.8187G>T - r.(?) p.(Lys2729Asn) - ClinVar Unknown g.32363389G>T - E Thirthagiri et al. (2008),dbSNP,ClinVar BRCA2_000032 rs80359065 - - - - - - - - - - - - - -
-/. - c.8187G>T - r.(?) p.(Lys2729Asn) - ClinVar Unknown g.32363389G>T - Kah Nyin Lai et al. (2017), dbSNP, ClinVar BRCA2_000032 rs80359065 15/1218 - DNA ? BRCA2 Kah Nyin Lai et al. (2017) F Malaysia - - - - 1 Nuur Athirah Binti Mohd Daud
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