ClinVar Miner

List of variants in gene CACNA1S reported as likely benign by Invitae

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Total variants: 60
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HGVS dbSNP
NM_000069.3(CACNA1S):c.1383C>G (p.Thr461=) rs144920422
NM_000069.3(CACNA1S):c.159C>T (p.Phe53=) rs199720439
NM_000069.3(CACNA1S):c.1704C>A (p.Leu568=) rs201748367
NM_000069.3(CACNA1S):c.1845C>T (p.Asp615=) rs200091030
NM_000069.3(CACNA1S):c.1890G>A (p.Pro630=) rs141717649
NM_000069.3(CACNA1S):c.1903A>G (p.Met635Val) rs201784750
NM_000069.3(CACNA1S):c.1935C>T (p.Phe645=) rs550584336
NM_000069.3(CACNA1S):c.1949-7C>T rs368564115
NM_000069.3(CACNA1S):c.2100G>A (p.Thr700=) rs774160640
NM_000069.3(CACNA1S):c.2187C>T (p.Val729=) rs770255183
NM_000069.3(CACNA1S):c.2331C>T (p.Ser777=) rs749013125
NM_000069.3(CACNA1S):c.2361-10G>A rs533238983
NM_000069.3(CACNA1S):c.2376T>C (p.Cys792=) rs528604695
NM_000069.3(CACNA1S):c.2439C>T (p.Ser813=) rs376863448
NM_000069.3(CACNA1S):c.2440G>A (p.Ala814Thr) rs139956524
NM_000069.3(CACNA1S):c.2556G>A (p.Thr852=) rs1160627876
NM_000069.3(CACNA1S):c.2562C>T (p.Tyr854=) rs373510147
NM_000069.3(CACNA1S):c.2657+10G>A rs371339601
NM_000069.3(CACNA1S):c.2657+9C>T rs375784883
NM_000069.3(CACNA1S):c.2658-9G>A rs367580345
NM_000069.3(CACNA1S):c.2694G>T (p.Val898=) rs1553250516
NM_000069.3(CACNA1S):c.2754G>A (p.Val918=) rs150708636
NM_000069.3(CACNA1S):c.2919C>T (p.Tyr973=) rs751043315
NM_000069.3(CACNA1S):c.2952G>A (p.Glu984=) rs1553250091
NM_000069.3(CACNA1S):c.2960A>G (p.His987Arg) rs201174511
NM_000069.3(CACNA1S):c.3144C>T (p.Tyr1048=) rs1468895414
NM_000069.3(CACNA1S):c.315C>T (p.Ile105=) rs756365041
NM_000069.3(CACNA1S):c.3177C>T (p.Ile1059=) rs1553249999
NM_000069.3(CACNA1S):c.3425A>C (p.Gln1142Pro) rs139373152
NM_000069.3(CACNA1S):c.345C>T (p.Asp115=) rs144218745
NM_000069.3(CACNA1S):c.3525+7del rs759199210
NM_000069.3(CACNA1S):c.3616C>T (p.Leu1206=) rs148105111
NM_000069.3(CACNA1S):c.3657C>T (p.Cys1219=) rs376781102
NM_000069.3(CACNA1S):c.3664G>A (p.Val1222Ile) rs202240111
NM_000069.3(CACNA1S):c.3777G>A (p.Thr1259=) rs147646714
NM_000069.3(CACNA1S):c.3807C>T (p.Tyr1269=) rs990173222
NM_000069.3(CACNA1S):c.3890G>A (p.Gly1297Glu) rs749856222
NM_000069.3(CACNA1S):c.4060A>T (p.Thr1354Ser) rs145910245
NM_000069.3(CACNA1S):c.4176C>G (p.Ser1392=) rs200935259
NM_000069.3(CACNA1S):c.4194C>T (p.His1398=) rs368919048
NM_000069.3(CACNA1S):c.4462G>A (p.Glu1488Lys) rs533353353
NM_000069.3(CACNA1S):c.460A>G (p.Ser154Gly) rs761768992
NM_000069.3(CACNA1S):c.4718C>T (p.Thr1573Met) rs183195890
NM_000069.3(CACNA1S):c.4747G>A (p.Glu1583Lys) rs148273582
NM_000069.3(CACNA1S):c.4752G>A (p.Leu1584=) rs763069723
NM_000069.3(CACNA1S):c.4962C>T (p.Asn1654=) rs370339547
NM_000069.3(CACNA1S):c.4995C>T (p.Asn1665=) rs183440052
NM_000069.3(CACNA1S):c.5049-2A>G rs148989517
NM_000069.3(CACNA1S):c.5199A>G (p.Arg1733=) rs1490186766
NM_000069.3(CACNA1S):c.5238G>A (p.Val1746=) rs374660431
NM_000069.3(CACNA1S):c.5299C>A (p.Pro1767Thr) rs200434921
NM_000069.3(CACNA1S):c.5356C>T (p.Leu1786=) rs371876697
NM_000069.3(CACNA1S):c.5388C>T (p.Gly1796=) rs1553247345
NM_000069.3(CACNA1S):c.541+7G>A rs1218931598
NM_000069.3(CACNA1S):c.5510A>C (p.Glu1837Ala) rs200765341
NM_000069.3(CACNA1S):c.5554G>A (p.Gly1852Arg) rs540721779
NM_000069.3(CACNA1S):c.5570G>A (p.Ser1857Asn) rs72749169
NM_000069.3(CACNA1S):c.5592C>T (p.Ser1864=) rs751405561
NM_000069.3(CACNA1S):c.639C>T (p.Ile213=) rs1229722414
NM_000069.3(CACNA1S):c.708G>C (p.Thr236=) rs754213830

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