ClinVar Miner

List of variants in gene TACR3 studied for reproductive system disorder

Included ClinVar conditions (663):
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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001059.3(TACR3):c.*73C>T rs2765 0.63284
NM_001059.3(TACR3):c.-103T>C rs3733632 0.34326
NM_001059.3(TACR3):c.873A>G (p.Leu291=) rs35085919 0.01614
NM_001059.3(TACR3):c.921A>C (p.Thr307=) rs34550211 0.01359
NM_001059.3(TACR3):c.857A>G (p.Lys286Arg) rs2276973 0.00877
NM_001059.3(TACR3):c.-20G>A rs201377092 0.00433
NM_001059.3(TACR3):c.579C>T (p.Pro193=) rs62340657 0.00164
NM_001059.3(TACR3):c.1344C>T (p.Ser448=) rs76121575 0.00160
NM_001059.3(TACR3):c.1246A>T (p.Asn416Tyr) rs143073792 0.00151
NM_001059.3(TACR3):c.*138G>A rs200193311 0.00041
NM_001059.3(TACR3):c.824G>A (p.Trp275Ter) rs144292455 0.00039
NM_001059.3(TACR3):c.1321C>T (p.Arg441Cys) rs146482011 0.00024
NM_001059.3(TACR3):c.-10A>T rs200498239 0.00017
NM_001059.3(TACR3):c.1290G>A (p.Thr430=) rs138661164 0.00015
NM_001059.3(TACR3):c.918G>A (p.Met306Ile) rs201088165 0.00006
NM_001059.3(TACR3):c.*87T>C rs199959009 0.00004
NM_001059.3(TACR3):c.*143G>A rs145839786 0.00003
NM_001059.3(TACR3):c.1206C>T (p.Thr402=) rs201120800 0.00003
NM_001059.3(TACR3):c.692C>T (p.Thr231Ile) rs764659822 0.00003
NM_001059.3(TACR3):c.737C>T (p.Thr246Ile) rs200991185 0.00003
NM_001059.3(TACR3):c.743A>G (p.His248Arg) rs1374236686 0.00003
NM_001059.3(TACR3):c.*125A>G rs201125726 0.00001
NM_001059.3(TACR3):c.-111C>A rs371989130 0.00001
NM_001059.3(TACR3):c.114G>T (p.Glu38Asp) rs886058977 0.00001
NM_001059.3(TACR3):c.1234G>A (p.Val412Met) rs151158699 0.00001
NM_001059.3(TACR3):c.1289C>T (p.Thr430Met) rs200736098 0.00001
NM_001059.3(TACR3):c.150C>T (p.Asn50=) rs201531776 0.00001
NM_001059.3(TACR3):c.278G>A (p.Gly93Asp) rs121918124 0.00001
NM_001059.3(TACR3):c.623G>A (p.Trp208Ter) rs727505375 0.00001
NM_001059.3(TACR3):c.688C>T (p.Arg230Cys) rs1195516345 0.00001
NM_001059.3(TACR3):c.737+1G>A rs760022956 0.00001
NM_001059.3(TACR3):c.*202G>C rs886058970
NM_001059.3(TACR3):c.*94T>G rs1723845345
NM_001059.3(TACR3):c.-20G>C rs201377092
NM_001059.3(TACR3):c.-86C>A rs886058978
NM_001059.3(TACR3):c.-93A>G rs1723174170
NM_001059.3(TACR3):c.1003C>T (p.Gln335Ter)
NM_001059.3(TACR3):c.1057C>T (p.Pro353Ser) rs121918125
NM_001059.3(TACR3):c.1188G>A (p.Arg396=) rs886058974
NM_001059.3(TACR3):c.1225A>G (p.Met409Val) rs201828791
NM_001059.3(TACR3):c.1230A>T (p.Thr410=) rs886058973
NM_001059.3(TACR3):c.1311T>C (p.Asn437=) rs886058972
NM_001059.3(TACR3):c.1345G>A (p.Ala449Thr) rs17033889
NM_001059.3(TACR3):c.1345G>T (p.Ala449Ser) rs17033889
NM_001059.3(TACR3):c.138C>T (p.Asp46=) rs181951458
NM_001059.3(TACR3):c.548+2T>A rs772508077
NM_001059.3(TACR3):c.703G>A (p.Val235Met) rs886058976
NM_001059.3(TACR3):c.766T>C (p.Tyr256His) rs397515483
NM_001059.3(TACR3):c.947A>G (p.His316Arg)

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