ClinVar Miner

List of variants reported as likely benign for breast-ovarian cancer, familial, susceptibility to, 4 by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 82
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HGVS dbSNP
NM_002878.3(RAD51D):c.105C>T (p.Asp35=) rs1555570413
NM_002878.3(RAD51D):c.108G>A (p.Leu36=) rs755962971
NM_002878.3(RAD51D):c.126A>G (p.Lys42=) rs145361433
NM_002878.3(RAD51D):c.12C>G (p.Leu4=) rs786203193
NM_002878.3(RAD51D):c.144+8C>T rs1060504766
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.145-9C>T rs1555570311
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
NM_002878.3(RAD51D):c.165G>C (p.Arg55=) rs1555570292
NM_002878.3(RAD51D):c.171G>A (p.Leu57=) rs786202885
NM_002878.3(RAD51D):c.186G>A (p.Ser62=) rs746984258
NM_002878.3(RAD51D):c.195C>T (p.Pro65=) rs376616485
NM_002878.3(RAD51D):c.196G>A (p.Val66Met) rs56026142
NM_002878.3(RAD51D):c.198G>T (p.Val66=) rs200810304
NM_002878.3(RAD51D):c.204C>A (p.Gly68=) rs764351040
NM_002878.3(RAD51D):c.204C>T (p.Gly68=) rs764351040
NM_002878.3(RAD51D):c.223C>T (p.Leu75=) rs746929682
NM_002878.3(RAD51D):c.22C>T (p.Leu8=) rs876659203
NM_002878.3(RAD51D):c.231C>G (p.Thr77=) rs376670250
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.264-8G>A rs759532599
NM_002878.3(RAD51D):c.27C>T (p.Cys9=) rs200487648
NM_002878.3(RAD51D):c.324C>T (p.Gly108=) rs758132417
NM_002878.3(RAD51D):c.333C>T (p.Ser111=) rs369396909
NM_002878.3(RAD51D):c.33C>T (p.Gly11=) rs760444811
NM_002878.3(RAD51D):c.346-10C>T rs779972784
NM_002878.3(RAD51D):c.346-4C>G rs767328693
NM_002878.3(RAD51D):c.346-7C>T rs1060504768
NM_002878.3(RAD51D):c.346-8A>G rs756059587
NM_002878.3(RAD51D):c.346-8A>T rs756059587
NM_002878.3(RAD51D):c.346-9C>A rs878854563
NM_002878.3(RAD51D):c.382C>T (p.Leu128=) rs1438461174
NM_002878.3(RAD51D):c.39C>G (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.438C>T (p.Leu146=) rs145452047
NM_002878.3(RAD51D):c.445C>T (p.Leu149=) rs1555568301
NM_002878.3(RAD51D):c.456T>C (p.Ala152=) rs921214343
NM_002878.3(RAD51D):c.481-10A>G rs1555568182
NM_002878.3(RAD51D):c.481-4T>G rs876659339
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.507G>A (p.Val169=) rs1555568162
NM_002878.3(RAD51D):c.510G>A (p.Val170=) rs142134504
NM_002878.3(RAD51D):c.549G>A (p.Gln183=) rs1555568122
NM_002878.3(RAD51D):c.567G>A (p.Val189=) rs373975416
NM_002878.3(RAD51D):c.570C>T (p.Ala190=) rs750479232
NM_002878.3(RAD51D):c.577-10A>C rs1060504767
NM_002878.3(RAD51D):c.577-10A>G rs1060504767
NM_002878.3(RAD51D):c.577-7C>T rs1438561890
NM_002878.3(RAD51D):c.600G>T (p.Val200=) rs755393515
NM_002878.3(RAD51D):c.606G>C (p.Val202=) rs1555567627
NM_002878.3(RAD51D):c.621G>A (p.Ser207=) rs749859221
NM_002878.3(RAD51D):c.621G>T (p.Ser207=) rs749859221
NM_002878.3(RAD51D):c.627T>C (p.Thr209=) rs141545966
NM_002878.3(RAD51D):c.667+9T>C rs772193051
NM_002878.3(RAD51D):c.668-4G>A rs1001440122
NM_002878.3(RAD51D):c.668-9C>T rs1555567544
NM_002878.3(RAD51D):c.66C>T (p.Ser22=) rs876660902
NM_002878.3(RAD51D):c.690G>A (p.Leu230=) rs1555567526
NM_002878.3(RAD51D):c.694C>A (p.Arg232=) rs587780104
NM_002878.3(RAD51D):c.6C>A (p.Gly2=) rs1255954226
NM_002878.3(RAD51D):c.738+10C>A rs777453585
NM_002878.3(RAD51D):c.739-10T>C rs199998187
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.75C>T (p.Ile25=) rs1555570482
NM_002878.3(RAD51D):c.765G>A (p.Arg255=) rs751833940
NM_002878.3(RAD51D):c.792C>G (p.Leu264=) rs536544621
NM_002878.3(RAD51D):c.792C>T (p.Leu264=) rs536544621
NM_002878.3(RAD51D):c.823C>A (p.Arg275=) rs752780416
NM_002878.3(RAD51D):c.840C>T (p.Thr280=) rs751885496
NM_002878.3(RAD51D):c.843C>T (p.Ile281=) rs754455433
NM_002878.3(RAD51D):c.849A>C (p.Gly283=) rs766847072
NM_002878.3(RAD51D):c.864C>T (p.Gly288=) rs138557828
NM_002878.3(RAD51D):c.879G>A (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.879G>C (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.879G>T (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.888C>G (p.Ala296=) rs755177638
NM_002878.3(RAD51D):c.900A>G (p.Arg300=) rs370634278
NM_002878.3(RAD51D):c.90C>T (p.Asp30=) rs374725981
NM_002878.3(RAD51D):c.919G>A (p.Glu307Lys) rs115031549
NM_002878.3(RAD51D):c.932T>A (p.Ile311Asn) rs145309168
NM_002878.3(RAD51D):c.957G>A (p.Gln319=) rs147669627
NM_002878.3(RAD51D):c.966A>G (p.Thr322=) rs786203299
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595

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