Full data view for gene BRCA2

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

3 entries on 1 page. Showing entries 1 - 3.
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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     
?/. 23 c.9104A>G - r.(?) p.(Tyr3035Cys) - ClinVar Unknown g.32379900A>G - E Thirthagiri et al. (2008), dbSNP ,ClinVar BRCA2_000035 rs80359165 - - - - - - - - - - - - - -
./. - c.9104A>G - r.(?) p.(Tyr3035Cys) - ClinVar Unknown g.32379900A>G - Kah Nyin Lai et al. (2017), dbSNP, ClinVar BRCA2_000035 rs80359165 2/1213 - DNA ? BRCA2 Kah Nyin Lai et al. (2017) F Malaysia - - - - 1 Nuur Athirah Binti Mohd Daud
+/. - c.9104A>G - r.(?) p.(Tyr3035Cys) missense Uncertain significance​ / Likely benign Unknown g.32379900A>G - Wei Xiong Wen et al. (2018), dbSNP, ClinVar BRCA2_000035 rs80359165 3/1762 VUS (variants of unknown significance) DNA MLPA, SEQ-NG-I BRCA2 Wei Xiong Wen et al. (2018) - Malaysia Chinese - - - 1 Nuur Athirah Binti Mohd Daud
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