ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_000059.3(BRCA2):c.1295A>C (p.Glu432Ala) rs1161226532
NM_000059.3(BRCA2):c.1340C>T (p.Pro447Leu) rs587776459
NM_000059.3(BRCA2):c.2524G>C (p.Val842Leu) rs587782454
NM_000059.3(BRCA2):c.3382A>G (p.Thr1128Ala) rs730881523
NM_000059.3(BRCA2):c.449A>G (p.His150Arg) rs397507722
NM_000059.3(BRCA2):c.5070A>C (p.Lys1690Asn) rs56087561
NM_000059.3(BRCA2):c.5885T>C (p.Ile1962Thr) rs1060502377
NM_000059.3(BRCA2):c.6423T>G (p.Gly2141=) rs780721021
NM_000059.3(BRCA2):c.6734T>A (p.Leu2245Gln) rs772795886
NM_000059.3(BRCA2):c.6937+565T>C rs11571675
NM_000059.3(BRCA2):c.7504C>T (p.Arg2502Cys) rs55716624
NM_000059.3(BRCA2):c.7628A>G (p.Tyr2543Cys) rs431825354
NM_000059.3(BRCA2):c.7931A>G (p.Asn2644Ser) rs80359020
NM_000059.3(BRCA2):c.8029G>A (p.Glu2677Lys) rs1555286958
NM_000059.3(BRCA2):c.8355T>C (p.Pro2785=) rs1057524419
NM_000059.3(BRCA2):c.8487+133C>T rs797045413
NM_000059.3(BRCA2):c.8488-5T>C rs533806629
NM_000059.3(BRCA2):c.8953+5del rs797045414

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