ClinVar Miner

List of variants in gene CACNA1A reported as likely benign for History of neurodevelopmental disorder

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Total variants: 42
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HGVS dbSNP
NM_001127221.1(CACNA1A):c.1083-4C>G rs201056216
NM_001127221.1(CACNA1A):c.1398G>A (p.Ser466=) rs374307014
NM_001127221.1(CACNA1A):c.1548C>T (p.Ser516=) rs372275167
NM_001127221.1(CACNA1A):c.1575T>A (p.Ile525=) rs16010
NM_001127221.1(CACNA1A):c.1596C>T (p.Ser532=) rs372090886
NM_001127221.1(CACNA1A):c.1617C>T (p.Tyr539=) rs182505786
NM_001127221.1(CACNA1A):c.1626G>A (p.Gly542=) rs375628894
NM_001127221.1(CACNA1A):c.1695G>A (p.Glu565=)
NM_001127221.1(CACNA1A):c.1917-4G>A rs191026552
NM_001127221.1(CACNA1A):c.1992C>T (p.Ile664=) rs764413479
NM_001127221.1(CACNA1A):c.2013C>T (p.Asn671=)
NM_001127221.1(CACNA1A):c.2049C>T (p.Gly683=) rs535077726
NM_001127221.1(CACNA1A):c.2259C>T (p.Ser753=)
NM_001127221.1(CACNA1A):c.2400G>A (p.Pro800=) rs996453280
NM_001127221.1(CACNA1A):c.2826G>A (p.Glu942=) rs374511141
NM_001127221.1(CACNA1A):c.2958G>C (p.Pro986=) rs749357610
NM_001127221.1(CACNA1A):c.2971_2976GAGGGC[4] (p.991_992EG[4]) rs764399373
NM_001127221.1(CACNA1A):c.3043G>A (p.Glu1015Lys) rs16024
NM_001127221.1(CACNA1A):c.3230C>T (p.Ala1077Val) rs199512932
NM_001127221.1(CACNA1A):c.3307G>A (p.Asp1103Asn) rs372823282
NM_001127221.1(CACNA1A):c.3412C>G (p.Pro1138Ala) rs199793367
NM_001127221.1(CACNA1A):c.3424G>A (p.Glu1142Lys)
NM_001127221.1(CACNA1A):c.357G>A (p.Gln119=) rs1568661972
NM_001127221.1(CACNA1A):c.3729G>A (p.Leu1243=) rs1568491811
NM_001127221.1(CACNA1A):c.4224C>T (p.Asp1408=) rs201200430
NM_001127221.1(CACNA1A):c.4314G>A (p.Lys1438=) rs572036869
NM_001127221.1(CACNA1A):c.4635C>T (p.Thr1545=) rs150378053
NM_001127221.1(CACNA1A):c.5091G>A (p.Leu1697=)
NM_001127221.1(CACNA1A):c.5421C>T (p.Val1807=)
NM_001127221.1(CACNA1A):c.5652C>G (p.Pro1884=) rs61741139
NM_001127221.1(CACNA1A):c.5653G>A (p.Val1885Ile) rs201836062
NM_001127221.1(CACNA1A):c.5655C>T (p.Val1885=) rs17846921
NM_001127221.1(CACNA1A):c.5688C>T (p.Thr1896=) rs757291476
NM_001127221.1(CACNA1A):c.5900G>A (p.Arg1967Gln) rs199886234
NM_001127221.1(CACNA1A):c.6064G>A (p.Glu2022Lys) rs202002033
NM_001127221.1(CACNA1A):c.6268C>A (p.Arg2090=) rs200093958
NM_001127221.1(CACNA1A):c.633T>C (p.Ser211=) rs202216404
NM_001127221.1(CACNA1A):c.6467G>A (p.Arg2156His) rs572722130
NM_001127221.1(CACNA1A):c.6467G>T (p.Arg2156Leu) rs572722130
NM_001127221.1(CACNA1A):c.6653_6661del (p.His2218_His2220del) rs776181081
NM_001127221.1(CACNA1A):c.6670C>T (p.Pro2224Ser)
NM_001127221.1(CACNA1A):c.6672C>A (p.Pro2224=)

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