ClinVar Miner

List of variants in gene combination LOC129390903, RAD51C reported as uncertain significance for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.640C>T (p.Arg214Cys) rs140804406 0.00017
NM_058216.3(RAD51C):c.635G>A (p.Arg212His) rs200857129 0.00004
NM_058216.3(RAD51C):c.704A>C (p.Lys235Thr) rs748043225 0.00002
NM_058216.3(RAD51C):c.601C>G (p.Leu201Val) rs531838785 0.00001
NM_058216.3(RAD51C):c.607A>G (p.Asn203Asp) rs538884532 0.00001
NM_058216.3(RAD51C):c.620A>G (p.His207Arg) rs587781921 0.00001
NM_058216.3(RAD51C):c.621T>A (p.His207Gln) rs786201848 0.00001
NM_058216.3(RAD51C):c.622A>G (p.Ile208Val) rs771078849 0.00001
NM_058216.3(RAD51C):c.634C>T (p.Arg212Cys) rs137947462 0.00001
NM_058216.3(RAD51C):c.641G>A (p.Arg214His) rs760911964 0.00001
NM_058216.3(RAD51C):c.644A>G (p.Asp215Gly) rs1483938000 0.00001
NM_058216.3(RAD51C):c.653A>G (p.Glu218Gly) rs1321358603 0.00001
NM_058216.3(RAD51C):c.656T>C (p.Leu219Ser) rs201529791 0.00001
NM_058216.3(RAD51C):c.680C>T (p.Pro227Leu) rs1374461662 0.00001
NM_058216.3(RAD51C):c.687C>G (p.Phe229Leu) rs780177888 0.00001
NM_058216.3(RAD51C):c.601C>T (p.Leu201Phe)
NM_058216.3(RAD51C):c.602T>C (p.Leu201Pro) rs587780839
NM_058216.3(RAD51C):c.602T>G (p.Leu201Arg)
NM_058216.3(RAD51C):c.605A>G (p.Asp202Gly) rs1060502591
NM_058216.3(RAD51C):c.606T>A (p.Asp202Glu) rs2048270218
NM_058216.3(RAD51C):c.608A>G (p.Asn203Ser)
NM_058216.3(RAD51C):c.610A>G (p.Ile204Val) rs1598473225
NM_058216.3(RAD51C):c.617C>A (p.Ser206Tyr)
NM_058216.3(RAD51C):c.620A>T (p.His207Leu)
NM_058216.3(RAD51C):c.622A>T (p.Ile208Phe)
NM_058216.3(RAD51C):c.623T>G (p.Ile208Ser) rs1598473279
NM_058216.3(RAD51C):c.624T>G (p.Ile208Met) rs775006411
NM_058216.3(RAD51C):c.625T>G (p.Tyr209Asp) rs2143798413
NM_058216.3(RAD51C):c.626A>T (p.Tyr209Phe) rs1017384420
NM_058216.3(RAD51C):c.629A>G (p.Tyr210Cys) rs1598473310
NM_058216.3(RAD51C):c.631T>C (p.Phe211Leu) rs2048271607
NM_058216.3(RAD51C):c.634C>A (p.Arg212Ser) rs137947462
NM_058216.3(RAD51C):c.634C>G (p.Arg212Gly) rs137947462
NM_058216.3(RAD51C):c.635G>T (p.Arg212Leu) rs200857129
NM_058216.3(RAD51C):c.637T>C (p.Cys213Arg)
NM_058216.3(RAD51C):c.638G>C (p.Cys213Ser) rs2143798852
NM_058216.3(RAD51C):c.645C>G (p.Asp215Glu) rs2143799278
NM_058216.3(RAD51C):c.647A>G (p.Tyr216Cys) rs746755735
NM_058216.3(RAD51C):c.649A>C (p.Thr217Pro)
NM_058216.3(RAD51C):c.649A>G (p.Thr217Ala) rs1555597189
NM_058216.3(RAD51C):c.649A>T (p.Thr217Ser) rs1555597189
NM_058216.3(RAD51C):c.658C>G (p.Leu220Val)
NM_058216.3(RAD51C):c.659T>C (p.Leu220Pro)
NM_058216.3(RAD51C):c.667G>A (p.Val223Ile) rs876660177
NM_058216.3(RAD51C):c.670_705+64dup rs1555597210
NM_058216.3(RAD51C):c.671A>G (p.Tyr224Cys) rs730881924
NM_058216.3(RAD51C):c.672_705+65dup rs1555597214
NM_058216.3(RAD51C):c.674T>C (p.Leu225Pro) rs1032681872
NM_058216.3(RAD51C):c.674TTC[1] (p.Leu226del) rs1555597217
NM_058216.3(RAD51C):c.677T>C (p.Leu226Pro) rs1225858240
NM_058216.3(RAD51C):c.679C>T (p.Pro227Ser) rs958242201
NM_058216.3(RAD51C):c.683A>G (p.Asp228Gly) rs2048274960
NM_058216.3(RAD51C):c.683A>T (p.Asp228Val) rs2048274960
NM_058216.3(RAD51C):c.685T>A (p.Phe229Ile)
NM_058216.3(RAD51C):c.688C>T (p.Leu230Phe) rs751528808
NM_058216.3(RAD51C):c.692C>T (p.Ser231Leu) rs1060502588
NM_058216.3(RAD51C):c.694G>A (p.Glu232Lys) rs2143801948
NM_058216.3(RAD51C):c.696A>T (p.Glu232Asp) rs786201177
NM_058216.3(RAD51C):c.697C>T (p.His233Tyr) rs2143802148
NM_058216.3(RAD51C):c.698A>C (p.His233Pro)
NM_058216.3(RAD51C):c.698A>G (p.His233Arg) rs754895072
NM_058216.3(RAD51C):c.703A>G (p.Lys235Glu) rs1555597252
NM_058216.3(RAD51C):c.705+3A>G rs878855179
NM_058216.3(RAD51C):c.705+3A>T rs878855179
NM_058216.3(RAD51C):c.705+4T>G rs778157321
NM_058216.3(RAD51C):c.705+6A>C
NM_058216.3(RAD51C):c.705G>T (p.Lys235Asn) rs755849719

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