ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by Mayo Clinic Genetic Testing Laboratories,Mayo Clinic

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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_000059.3(BRCA2):c.2944A>C (p.Ile982Leu) rs28897717
NM_000059.3(BRCA2):c.3858A>T (p.Lys1286Asn) rs1555283430
NM_000059.3(BRCA2):c.4045A>G (p.Ile1349Val) rs780544697
NM_000059.3(BRCA2):c.5554G>A (p.Val1852Ile) rs80358777
NM_000059.3(BRCA2):c.5737T>C (p.Cys1913Arg) rs80358799
NM_000059.3(BRCA2):c.5884A>G (p.Ile1962Val) rs747406932
NM_000059.3(BRCA2):c.7154T>G (p.Val2385Gly) rs1555286021
NM_000059.3(BRCA2):c.7429C>A (p.Pro2477Thr) rs80358964
NM_000059.3(BRCA2):c.7540A>G (p.Lys2514Glu) rs864622624
NM_000059.3(BRCA2):c.7630G>A (p.Gly2544Ser) rs587781485
NM_000059.3(BRCA2):c.793+6T>C rs1222477192
NM_000059.3(BRCA2):c.8128A>G (p.Ser2710Gly) rs398122597
NM_000059.3(BRCA2):c.8149G>T (p.Ala2717Ser) rs28897747
NM_000059.3(BRCA2):c.865A>G (p.Asn289Asp) rs766173
NM_000059.3(BRCA2):c.9190G>A (p.Asp3064Asn) rs80359177

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