ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by Pathway Genomics

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Total variants: 10
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HGVS dbSNP
NM_000059.3(BRCA2):c.2138A>C (p.Gln713Pro) rs55816687
NM_000059.3(BRCA2):c.4436G>C (p.Ser1479Thr) rs80358678
NM_000059.3(BRCA2):c.467A>G (p.Asp156Gly) rs68071147
NM_000059.3(BRCA2):c.5035A>G (p.Thr1679Ala) rs80358728
NM_000059.3(BRCA2):c.566A>G (p.Asp189Gly) rs397507359
NM_000059.3(BRCA2):c.5982A>T (p.Gln1994His) rs587783043
NM_000059.3(BRCA2):c.6257T>C (p.Ile2086Thr) rs587783042
NM_000059.3(BRCA2):c.7987G>A (p.Glu2663Lys) rs80359030
NM_000059.3(BRCA2):c.8087T>G (p.Leu2696Trp) rs80359050
NM_000059.3(BRCA2):c.8423T>C (p.Leu2808Pro) rs587783044

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