ClinVar Miner

List of variants reported as likely pathogenic for Neoplasm of ovary

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Total variants: 32
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HGVS dbSNP
NC_012920.1:m.14743A>G rs527236161
NC_012920.1:m.14753C>T rs527236162
NC_012920.1:m.14784T>C rs527236163
NC_012920.1:m.15058C>T rs527236171
NC_012920.1:m.15061A>G rs527236205
NC_012920.1:m.15098A>G rs527236172
NC_012920.1:m.15148G>A rs527236206
NC_012920.1:m.15259C>T rs527236207
NC_012920.1:m.15314G>A rs527236176
NC_012920.1:m.15328A>G rs527236178
NC_012920.1:m.15334C>T rs527236179
NC_012920.1:m.15363A>G rs527236182
NC_012920.1:m.15431G>A rs193302993
NC_012920.1:m.15452C>A rs193302994
NC_012920.1:m.15453T>C rs527236184
NC_012920.1:m.15459C>T rs527236186
NC_012920.1:m.15511T>C rs527236188
NC_012920.1:m.15607A>G rs193302996
NC_012920.1:m.15670T>C rs193302997
NC_012920.1:m.15884G>A rs527236195
NC_012920.1:m.15890C>A rs527236196
NC_012920.1:m.15928G>A rs527236198
NC_012920.1:m.15932T>G rs527236199
NC_012920.1:m.15943T>C rs527236200
NM_032043.2(BRIP1):c.1240C>T (p.Gln414Ter) rs368796923
NM_032043.2(BRIP1):c.1853_1854insG (p.Pro619fs) rs587781985
NM_032043.2(BRIP1):c.2038_2039dup (p.Leu680fs) rs587778134
NM_032043.2(BRIP1):c.205+1delG rs1057517648
NM_032043.2(BRIP1):c.2111T>A (p.Leu704Ter) rs1057517643
NM_032043.2(BRIP1):c.2392C>T (p.Arg798Ter) rs137852986
NM_032043.2(BRIP1):c.286_289ACAA[1] (p.Asn97fs) rs763009188
NM_032043.2(BRIP1):c.2982_2985CAAA[2] (p.Thr997fs) rs771028677

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