ClinVar Miner

List of variants in gene CASR reported as benign for not specified

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Total variants: 15
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HGVS dbSNP
NM_000388.3(CASR):c.1285C>T (p.His429Tyr) rs142818334
NM_000388.3(CASR):c.1333A>G (p.Thr445Ala) rs12493789
NM_000388.3(CASR):c.1775A>G (p.Asn592Ser) rs117375173
NM_000388.3(CASR):c.2244C= (p.Pro748=) rs2036400
NM_000388.3(CASR):c.2610G>A (p.Glu870=) rs143738711
NM_000388.3(CASR):c.2730C>A (p.Pro910=) rs34200949
NM_000388.3(CASR):c.3031C= (p.Gln1011=) rs1801726
NM_000388.3(CASR):c.3031C>G (p.Gln1011Glu) rs1801726
NM_000388.3(CASR):c.492+19G>A rs9869985
NM_000388.3(CASR):c.573G>A (p.Glu191=) rs141631116
NM_000388.3(CASR):c.748G>A (p.Glu250Lys) rs62269092
NM_000388.3(CASR):c.78C>G (p.Ala26=) rs77852524
NM_001178065.1(CASR):c.1762+16T>C rs2270916
NM_001178065.1(CASR):c.2986G>T (p.Ala996Ser) rs1801725
NM_001178065.1(CASR):c.2998A>G (p.Arg1000Gly) rs1042636

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