ClinVar Miner

List of variants in gene CACNA1F reported by Ambry Genetics

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001256789.3(CACNA1F):c.4085T>C (p.Val1362Ala) rs200903890 0.00031
NM_001256789.3(CACNA1F):c.4222G>A (p.Ala1408Thr) rs782741094 0.00017
NM_001256789.3(CACNA1F):c.1537C>T (p.Arg513Trp) rs142532762 0.00012
NM_001256789.3(CACNA1F):c.1841G>A (p.Arg614Gln) rs782123232 0.00008
NM_001256789.3(CACNA1F):c.953T>C (p.Phe318Ser) rs201174690 0.00007
NM_001256789.3(CACNA1F):c.2848G>A (p.Ala950Thr) rs369730240 0.00006
NM_001256789.3(CACNA1F):c.1315C>T (p.Arg439Cys) rs782649560 0.00003
NM_001256789.3(CACNA1F):c.1322G>A (p.Arg441His) rs1234852260 0.00003
NM_001256789.3(CACNA1F):c.1538G>A (p.Arg513Gln) rs782288797 0.00003
NM_001256789.3(CACNA1F):c.4481G>T (p.Cys1494Phe) rs782025685 0.00003
NM_001256789.3(CACNA1F):c.1606G>A (p.Ala536Thr) rs781923856 0.00002
NM_001256789.3(CACNA1F):c.1778G>A (p.Gly593Asp) rs1557109497 0.00002
NM_001256789.3(CACNA1F):c.1414G>A (p.Gly472Ser) rs782254354 0.00001
NM_001256789.3(CACNA1F):c.1753T>G (p.Phe585Val) rs1557109510 0.00001
NM_001256789.3(CACNA1F):c.3808G>C (p.Gly1270Arg) rs1391559071 0.00001
NM_001256789.3(CACNA1F):c.5071A>G (p.Thr1691Ala) rs1198251463 0.00001
NM_001256789.3(CACNA1F):c.1264G>T (p.Asp422Tyr)
NM_001256789.3(CACNA1F):c.1298C>G (p.Thr433Ser)
NM_001256789.3(CACNA1F):c.1685C>T (p.Thr562Met)
NM_001256789.3(CACNA1F):c.1695G>A (p.Met565Ile)
NM_001256789.3(CACNA1F):c.1862T>C (p.Ile621Thr)
NM_001256789.3(CACNA1F):c.1957T>A (p.Phe653Ile)
NM_001256789.3(CACNA1F):c.22A>G (p.Lys8Glu)
NM_001256789.3(CACNA1F):c.3391G>T (p.Ala1131Ser) rs782258468
NM_001256789.3(CACNA1F):c.3734C>T (p.Thr1245Met)
NM_001256789.3(CACNA1F):c.3976A>C (p.Ile1326Leu)
NM_001256789.3(CACNA1F):c.3976A>G (p.Ile1326Val)
NM_001256789.3(CACNA1F):c.4393C>G (p.Arg1465Gly)

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