ClinVar Miner

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

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Gene type:
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Total variants: 14
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HGVS dbSNP
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.1377+17T>C rs200650843
NM_000388.4(CASR):c.1491C>T (p.Ser497=) rs150337940
NM_000388.4(CASR):c.1631G>A (p.Arg544Gln) rs115230894
NM_000388.4(CASR):c.1733-9A>G rs190731787
NM_000388.4(CASR):c.2412C>T (p.Ala804=) rs886038418
NM_000388.4(CASR):c.2824G>A (p.Glu942Lys) rs76327999
NM_000388.4(CASR):c.3091G>A (p.Gly1031Ser) rs142704083
NM_000388.4(CASR):c.492+18G>C rs540628385
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.6A>C (p.Ala2=) rs112042188
NM_000388.4(CASR):c.748G>A (p.Glu250Lys) rs62269092

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