ClinVar Miner

List of variants in gene AR studied for cancer

Included ClinVar conditions (475):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_000044.6(AR):c.2180G>T (p.Arg727Leu) rs137852593 0.00141
NM_000044.6(AR):c.2395C>G (p.Gln799Glu) rs137852591 0.00137
NM_000044.6(AR):c.170T>A (p.Leu57Gln) rs78686797 0.00112
NM_000044.6(AR):c.1792A>G (p.Ser598Gly) rs142280455 0.00038
NM_000044.6(AR):c.528C>A (p.Ser176Arg) rs777131133 0.00024
NM_000044.6(AR):c.1153G>T (p.Ala385Ser) rs200067740 0.00018
NM_000044.6(AR):c.1644G>T (p.Leu548Phe) rs139524801 0.00018
NM_000044.6(AR):c.1301C>T (p.Ser434Phe) rs748457992 0.00011
NM_000044.6(AR):c.1195T>C (p.Trp399Arg) rs774645775 0.00010
NM_000044.6(AR):c.1063G>C (p.Glu355Gln) rs367604031 0.00004
NM_000044.6(AR):c.1208C>T (p.Ala403Val) rs772490323 0.00003
NM_000044.6(AR):c.1651G>C (p.Asp551His) rs777461721 0.00002
NM_000044.6(AR):c.1885+3718A>G rs889696386 0.00002
NM_000044.6(AR):c.7G>A (p.Val3Met) rs778912582 0.00002
NM_000044.6(AR):c.1175C>G (p.Pro392Arg) rs773996740 0.00001
NM_000044.6(AR):c.2184C>G (p.Asn728Lys) rs768869912 0.00001
NM_000044.6(AR):c.2191G>A (p.Val731Met) rs137852571 0.00001
NM_000044.6(AR):c.1025C>T (p.Pro342Leu) rs138454018
NM_000044.6(AR):c.1157G>T (p.Arg386Leu)
NM_000044.6(AR):c.1186G>C (p.Gly396Arg)
NM_000044.6(AR):c.1360G>A (p.Gly454Arg)
NM_000044.6(AR):c.1370GCG[19] (p.Gly472_Gly473dup) rs746853821
NM_000044.6(AR):c.1421A>G (p.Glu474Gly)
NM_000044.6(AR):c.1484G>A (p.Ser495Asn)
NM_000044.6(AR):c.1585G>T (p.Asp529Tyr)
NM_000044.6(AR):c.161TGC[5] (p.Leu57dup) rs752055010
NM_000044.6(AR):c.1943G>A (p.Ser648Asn) rs137852584
NM_000044.6(AR):c.1976A>G (p.Lys659Arg)
NM_000044.6(AR):c.2105T>A (p.Leu702His) rs864622007
NM_000044.6(AR):c.2164G>A (p.Ala722Thr) rs137852583
NM_000044.6(AR):c.2207C>A (p.Ala736Asp)
NM_000044.6(AR):c.2599G>A (p.Val867Met) rs137852564
NM_000044.6(AR):c.2623C>T (p.His875Tyr) rs137852581
NM_000044.6(AR):c.2629T>C (p.Phe877Leu) rs1057519864
NM_000044.6(AR):c.2632A>G (p.Thr878Ala) rs137852578
NM_000044.6(AR):c.2633C>G (p.Thr878Ser) rs137852580
NM_000044.6(AR):c.2708A>G (p.Gln903Arg) rs137852582
NM_000044.6(AR):c.289C>T (p.Pro97Ser)
NM_000044.6(AR):c.626G>A (p.Gly209Glu)
NM_000044.6(AR):c.758C>T (p.Ala253Val)
NM_000044.6(AR):c.896C>T (p.Ala299Val)
NM_000044.6(AR):c.902A>G (p.Lys301Arg)

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