ClinVar Miner

List of variants in gene RAD51C reported as pathogenic for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NC_000017.10:g.(?_56769999)_(56787357_?)del
NC_000017.11:g.(?_58692638)_(58734228_?)del
NC_000017.11:g.(?_58696687)_(58696865_?)del
NC_000017.11:g.(?_58703196)_(58709990_?)del
NC_000017.11:g.(?_58709849)_(58734232_?)del
NC_000017.11:g.(?_58720740)_(58720818_?)del
NC_000017.11:g.(?_58720740)_(58724106_?)del
NC_000017.11:g.(?_58720746)_(58734342_?)del
NM_058216.1(RAD51C):c.(?_-1)_(*1_?)del
NM_058216.2(RAD51C):c.(?_-1)_837+?del
NM_058216.2(RAD51C):c.145+1G>T rs757128712
NM_058216.2(RAD51C):c.181_182delCT (p.Leu61Alafs) rs786203945
NM_058216.2(RAD51C):c.186_187delAA (p.Gln62Hisfs) rs587782170
NM_058216.2(RAD51C):c.199G>T (p.Glu67Ter)
NM_058216.2(RAD51C):c.250A>T (p.Lys84Ter) rs1555593616
NM_058216.2(RAD51C):c.312T>A (p.Cys104Ter) rs1555593715
NM_058216.2(RAD51C):c.31C>T (p.Gln11Ter)
NM_058216.2(RAD51C):c.363_371delAGAAATTTGinsC (p.Glu122Trpfs)
NM_058216.2(RAD51C):c.394dupA (p.Thr132Asnfs) rs730881940
NM_058216.2(RAD51C):c.397C>T (p.Gln133Ter) rs387907159
NM_058216.2(RAD51C):c.502A>T (p.Arg168Ter) rs587781490
NM_058216.2(RAD51C):c.50delT (p.Phe17Serfs) rs1555591851
NM_058216.2(RAD51C):c.535delC (p.His179Thrfs) rs1555594864
NM_058216.2(RAD51C):c.572-?_*(1_?)del
NM_058216.2(RAD51C):c.572-?_*120del
NM_058216.2(RAD51C):c.572-?_705+?del (p.(?))
NM_058216.2(RAD51C):c.577C>T (p.Arg193Ter) rs200293302
NM_058216.2(RAD51C):c.589G>T (p.Glu197Ter) rs1555597094
NM_058216.2(RAD51C):c.630T>G (p.Tyr210Ter) rs786201909
NM_058216.2(RAD51C):c.701C>G (p.Ser234Ter) rs587782818
NM_058216.2(RAD51C):c.706-2A>G rs587780259
NM_058216.2(RAD51C):c.706-?_*120del
NM_058216.2(RAD51C):c.709C>T (p.Arg237Ter) rs770637624
NM_058216.2(RAD51C):c.732delT (p.Ile244Metfs) rs1060502601
NM_058216.2(RAD51C):c.73delGinsTTC (p.Val25Phefs)
NM_058216.2(RAD51C):c.773G>A (p.Arg258His) rs267606997
NM_058216.2(RAD51C):c.774delT (p.Thr259Leufs) rs754367349
NM_058216.2(RAD51C):c.851_854delATCA (p.Asn284Argfs) rs1060502605
NM_058216.2(RAD51C):c.890_899delTTGTTCCTGC (p.Leu297Hisfs) rs1555602141
NM_058216.2(RAD51C):c.905-2A>C rs779582317
NM_058216.2(RAD51C):c.905-2A>G rs779582317
NM_058216.2(RAD51C):c.905-2_905-1delAG rs587781995
NM_058216.2(RAD51C):c.905-3_906delCAGGG rs730881941
NM_058216.2(RAD51C):c.914G>A (p.Trp305Ter) rs876659874
NM_058216.2(RAD51C):c.93delG (p.Phe32Serfs) rs730881942
NM_058216.2(RAD51C):c.955C>T (p.Arg319Ter) rs587781287
NM_058216.2(RAD51C):c.966-?_1026+?del
NM_058216.2(RAD51C):c.97C>T (p.Gln33Ter) rs587782528
NM_058216.2(RAD51C):c.97_98delCA (p.Gln33Aspfs) rs587780840
NM_058216.3(RAD51C):c.224dup (p.Tyr75Terfs) rs730881939
NM_058216.3(RAD51C):c.525dup (p.Cys176Leufs) rs768793789

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