ClinVar Miner

List of variants in gene RAD51C reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NC_000017.11:g.58692541G>A
NM_058216.3(RAD51C):c.*25C>G rs28363336
NM_058216.3(RAD51C):c.-26C>T rs12946397
NM_058216.3(RAD51C):c.1026+43C>T
NM_058216.3(RAD51C):c.114C>T (p.Leu38=) rs786202265
NM_058216.3(RAD51C):c.115C>T (p.Leu39=)
NM_058216.3(RAD51C):c.141C>T (p.Ser47=) rs568912602
NM_058216.3(RAD51C):c.145+11C>G rs1263551026
NM_058216.3(RAD51C):c.145+12T>G rs377297129
NM_058216.3(RAD51C):c.145+15T>C
NM_058216.3(RAD51C):c.146-15T>C rs1036386535
NM_058216.3(RAD51C):c.146-3C>T rs765143155
NM_058216.3(RAD51C):c.146-8A>G rs201079501
NM_058216.3(RAD51C):c.186A>G (p.Gln62=) rs28363303
NM_058216.3(RAD51C):c.195A>G (p.Arg65=) rs45511291
NM_058216.3(RAD51C):c.207C>T (p.Leu69=) rs1057523582
NM_058216.3(RAD51C):c.225T>C (p.Tyr75=) rs1555593553
NM_058216.3(RAD51C):c.234A>G (p.Thr78=) rs730881929
NM_058216.3(RAD51C):c.262C>T (p.Leu88=) rs786201383
NM_058216.3(RAD51C):c.270T>C (p.Leu90=) rs1555593651
NM_058216.3(RAD51C):c.336G>A (p.Gly112=) rs746122031
NM_058216.3(RAD51C):c.342A>G (p.Gly114=) rs1555593777
NM_058216.3(RAD51C):c.357A>G (p.Lys119=) rs863224434
NM_058216.3(RAD51C):c.376G>A (p.Ala126Thr) rs61758784
NM_058216.3(RAD51C):c.405-8G>A rs1431351072
NM_058216.3(RAD51C):c.405T>C (p.Cys135=) rs537272666
NM_058216.3(RAD51C):c.461A>G (p.Glu154Gly) rs758847241
NM_058216.3(RAD51C):c.477T>C (p.Asp159=) rs760436864
NM_058216.3(RAD51C):c.54G>T (p.Pro18=) rs1555591865
NM_058216.3(RAD51C):c.571+16A>G rs141621051
NM_058216.3(RAD51C):c.572-17G>T rs193023469
NM_058216.3(RAD51C):c.706-13C>G rs747406535
NM_058216.3(RAD51C):c.706-18T>C rs56401264
NM_058216.3(RAD51C):c.706-7T>C rs1555599087
NM_058216.3(RAD51C):c.717G>C (p.Val239=) rs1555599108
NM_058216.3(RAD51C):c.756A>G (p.Leu252=) rs863224437
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser) rs147241704
NM_058216.3(RAD51C):c.837+14A>G rs1057517644
NM_058216.3(RAD51C):c.837+7A>G rs1555599293
NM_058216.3(RAD51C):c.840A>G (p.Val280=) rs756503509
NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala) rs28363317
NM_058216.3(RAD51C):c.879T>C (p.Asn293=) rs1555602132
NM_058216.3(RAD51C):c.904+7A>C rs1555602171
NM_058216.3(RAD51C):c.905-7C>T rs757624360
NM_058216.3(RAD51C):c.90G>A (p.Ala30=) rs115414895

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