ClinVar Miner

List of variants in gene CASR studied for not specified

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Total variants: 50
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HGVS dbSNP
NM_000388.4(CASR):c.106G>A (p.Gly36Arg) rs193922420
NM_000388.4(CASR):c.1173C>T (p.Phe391=) rs998012311
NM_000388.4(CASR):c.1285C>T (p.His429Tyr) rs142818334
NM_000388.4(CASR):c.1333A>G (p.Thr445Ala) rs12493789
NM_000388.4(CASR):c.1377+17T>C rs200650843
NM_000388.4(CASR):c.1466A>G (p.Tyr489Cys) rs1553768108
NM_000388.4(CASR):c.1491C>T (p.Ser497=) rs150337940
NM_000388.4(CASR):c.1619C>T (p.Ser540Phe) rs1057518409
NM_000388.4(CASR):c.1631G>A (p.Arg544Gln) rs115230894
NM_000388.4(CASR):c.1732+16T>C rs2270916
NM_000388.4(CASR):c.1733-9A>G rs190731787
NM_000388.4(CASR):c.1765T>G (p.Phe589Val) rs1553768892
NM_000388.4(CASR):c.1775A>G (p.Asn592Ser) rs117375173
NM_000388.4(CASR):c.199G>C (p.Gly67Arg) rs1553766217
NM_000388.4(CASR):c.2045C>T (p.Pro682Leu) rs1553768989
NM_000388.4(CASR):c.2203C>A (p.Gln735Lys) rs1553769052
NM_000388.4(CASR):c.2216G>A (p.Cys739Tyr) rs375468610
NM_000388.4(CASR):c.2244G>C (p.Pro748=) rs2036400
NM_000388.4(CASR):c.2254C>T (p.Arg752Cys) rs193922434
NM_000388.4(CASR):c.2412C>T (p.Ala804=) rs886038418
NM_000388.4(CASR):c.2519C>T (p.Ala840Val) rs1553769127
NM_000388.4(CASR):c.2548G>A (p.Ala850Thr) rs1418475623
NM_000388.4(CASR):c.2549C>A (p.Ala850Glu) rs373819680
NM_000388.4(CASR):c.2610G>A (p.Glu870=) rs143738711
NM_000388.4(CASR):c.262C>T (p.Leu88Phe) rs1553766227
NM_000388.4(CASR):c.2638G>C (p.Ala880Pro) rs763865303
NM_000388.4(CASR):c.2730C>A (p.Pro910=) rs34200949
NM_000388.4(CASR):c.2824G>A (p.Glu942Lys) rs76327999
NM_000388.4(CASR):c.2956G>T (p.Ala986Ser) rs1801725
NM_000388.4(CASR):c.2968A>G (p.Arg990Gly) rs1042636
NM_000388.4(CASR):c.3031= (p.Glu1011=) rs1801726
NM_000388.4(CASR):c.3031G>C (p.Glu1011Gln) rs1801726
NM_000388.4(CASR):c.3091G>A (p.Gly1031Ser) rs142704083
NM_000388.4(CASR):c.377A>T (p.Asp126Val) rs1553766257
NM_000388.4(CASR):c.416T>C (p.Ile139Thr) rs1060502860
NM_000388.4(CASR):c.470T>C (p.Leu157Pro) rs1553766286
NM_000388.4(CASR):c.492+18G>C rs540628385
NM_000388.4(CASR):c.492+19G>A rs9869985
NM_000388.4(CASR):c.496A>G (p.Ser166Gly) rs193922441
NM_000388.4(CASR):c.513C>A (p.Ser171Arg) rs764149433
NM_000388.4(CASR):c.537A>G (p.Gln179=) rs200129212
NM_000388.4(CASR):c.546T>A (p.Ser182=) rs200545177
NM_000388.4(CASR):c.551T>C (p.Leu184Pro) rs1553766716
NM_000388.4(CASR):c.573G>A (p.Glu191=) rs141631116
NM_000388.4(CASR):c.587C>A (p.Ala196Asp) rs1553766728
NM_000388.4(CASR):c.6A>C (p.Ala2=) rs112042188
NM_000388.4(CASR):c.707G>A (p.Cys236Tyr) rs1057518616
NM_000388.4(CASR):c.748G>A (p.Glu250Lys) rs62269092
NM_000388.4(CASR):c.78C>G (p.Ala26=) rs77852524
NM_000388.4(CASR):c.89G>A (p.Gly30Glu) rs1553765889

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