ClinVar Miner

List of variants in gene CASR reported as benign

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
GRCh37/hg19 3q21.1(chr3:121933635-121943859)x1
GRCh37/hg19 3q21.1(chr3:121976494-121978343)x4
GRCh37/hg19 3q21.1(chr3:121976494-121979229)x4
NM_000388.4(CASR):c.*1015A>G rs9740
NM_000388.4(CASR):c.*1093C>T rs1802757
NM_000388.4(CASR):c.*1198T>C rs10190
NM_000388.4(CASR):c.*1235A>G rs34042920
NM_000388.4(CASR):c.*188dup rs33974189
NM_000388.4(CASR):c.*574C>G rs6438718
NM_000388.4(CASR):c.*60A>T rs4677948
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.165G>A (p.Pro55=) rs200018529
NM_000388.4(CASR):c.1732+16T>C rs2270916
NM_000388.4(CASR):c.1733-9A>G rs190731787
NM_000388.4(CASR):c.1775A>G (p.Asn592Ser) rs117375173
NM_000388.4(CASR):c.2064C>T (p.Phe688=) rs150869744
NM_000388.4(CASR):c.2244= (p.Pro748=) rs1553769059
NM_000388.4(CASR):c.2244G>C (p.Pro748=) rs2036400
NM_000388.4(CASR):c.2610G>A (p.Glu870=) rs143738711
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.3234A>T (p.Ser1078=) rs556263764
NM_000388.4(CASR):c.492+19G>A rs9869985
NM_000388.4(CASR):c.537A>G (p.Gln179=) rs200129212
NM_000388.4(CASR):c.573G>A (p.Glu191=) rs141631116
NM_000388.4(CASR):c.6A>C (p.Ala2=) rs112042188
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.906C>T (p.Ser302=) rs201067850
NM_000388.4(CASR):c.915C>A (p.Ile305=) rs200528343

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