ClinVar Miner

List of variants in gene CACNA1A reported as uncertain significance for History of neurodevelopmental disorder

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Total variants: 42
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HGVS dbSNP
NM_001127221.1(CACNA1A):c.1059C>A (p.Asn353Lys) rs1568546593
NM_001127221.1(CACNA1A):c.1121G>A (p.Arg374Gln)
NM_001127221.1(CACNA1A):c.1231G>T (p.Gly411Trp) rs1448345243
NM_001127221.1(CACNA1A):c.1364G>A (p.Arg455Gln) rs561858384
NM_001127221.1(CACNA1A):c.1493C>G (p.Ala498Gly) rs1568528100
NM_001127221.1(CACNA1A):c.1549G>A (p.Asp517Asn)
NM_001127221.1(CACNA1A):c.1699A>C (p.Ile567Leu) rs1568519066
NM_001127221.1(CACNA1A):c.2284A>G (p.Lys762Glu) rs1196111017
NM_001127221.1(CACNA1A):c.2407C>A (p.Arg803Ser) rs760816963
NM_001127221.1(CACNA1A):c.2498_2500ACA[2] (p.Asn835del) rs750962335
NM_001127221.1(CACNA1A):c.2504A>C (p.Asn835Thr)
NM_001127221.1(CACNA1A):c.2636A>T (p.Asp879Val) rs1568508904
NM_001127221.1(CACNA1A):c.2894C>A (p.Pro965His) rs1161926847
NM_001127221.1(CACNA1A):c.294-4A>G rs1400044284
NM_001127221.1(CACNA1A):c.3007A>G (p.Arg1003Gly) rs1175036875
NM_001127221.1(CACNA1A):c.3169C>T (p.Arg1057Cys) rs187393245
NM_001127221.1(CACNA1A):c.3250G>A (p.Gly1084Ser)
NM_001127221.1(CACNA1A):c.3268G>A (p.Gly1090Ser)
NM_001127221.1(CACNA1A):c.3432C>G (p.Ser1144Arg)
NM_001127221.1(CACNA1A):c.3637G>T (p.Asp1213Tyr) rs201269793
NM_001127221.1(CACNA1A):c.3727C>G (p.Leu1243Val) rs1275961783
NM_001127221.1(CACNA1A):c.3992C>T (p.Thr1331Ile)
NM_001127221.1(CACNA1A):c.4295G>A (p.Arg1432Gln)
NM_001127221.1(CACNA1A):c.4414G>A (p.Ala1472Thr) rs1187916307
NM_001127221.1(CACNA1A):c.4582G>C (p.Glu1528Gln) rs1568468148
NM_001127221.1(CACNA1A):c.4673G>A (p.Arg1558His) rs755172189
NM_001127221.1(CACNA1A):c.4687G>A (p.Val1563Met) rs1568465560
NM_001127221.1(CACNA1A):c.5158G>A (p.Asp1720Asn) rs368257155
NM_001127221.1(CACNA1A):c.5798A>G (p.Asn1933Ser) rs1205866071
NM_001127221.1(CACNA1A):c.5935G>A (p.Glu1979Lys) rs1266642291
NM_001127221.1(CACNA1A):c.6145G>A (p.Glu2049Lys) rs1568423655
NM_001127221.1(CACNA1A):c.6244T>C (p.Tyr2082His) rs1174830824
NM_001127221.1(CACNA1A):c.6382G>A (p.Val2128Met) rs368183370
NM_001127221.1(CACNA1A):c.6434C>T (p.Pro2145Leu) rs750077868
NM_001127221.1(CACNA1A):c.6470G>A (p.Arg2157His) rs755749925
NM_001127221.1(CACNA1A):c.6508C>T (p.Arg2170Cys) rs375354077
NM_001127221.1(CACNA1A):c.6530G>T (p.Gly2177Val) rs763045560
NM_001127221.1(CACNA1A):c.6644_6661del (p.His2215_His2220del) rs1453912866
NM_001127221.1(CACNA1A):c.6659A>C (p.His2220Pro)
NM_001127221.1(CACNA1A):c.6668C>T (p.Pro2223Leu) rs1336146310
NM_001127221.1(CACNA1A):c.6719G>A (p.Arg2240Gln)
NM_001127221.1(CACNA1A):c.6733C>T (p.Arg2245Cys)

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