ClinVar Miner

List of variants in gene CACNA1F reported as benign for not provided

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NC_000023.11:g.49233563= rs5906758 0.99896
NM_001256789.3(CACNA1F):c.3276C>T (p.His1092=) rs2075866 0.52573
NM_001256789.3(CACNA1F):c.4100+131G>C rs12009701 0.09780
NM_001256789.3(CACNA1F):c.1651+241A>G rs58793970 0.09695
NM_001256789.3(CACNA1F):c.818-302C>G rs7050910 0.09583
NM_001256789.3(CACNA1F):c.26-173C>G rs7066652 0.09508
NM_001256789.3(CACNA1F):c.2335-89C>T rs5906756 0.07887
NM_001256789.3(CACNA1F):c.5756G>A (p.Arg1919His) rs33910054 0.06102
NM_001256789.3(CACNA1F):c.3236+55T>C rs7066236 0.05349
NM_001256789.3(CACNA1F):c.2929-172C>T rs111247255 0.05297
NM_001256789.3(CACNA1F):c.521+39C>T rs112130833 0.05292
NM_001256789.3(CACNA1F):c.41C>T (p.Pro14Leu) rs6520408 0.05244
NM_001256789.3(CACNA1F):c.26-182A>G rs11796927 0.05142
NM_001256789.3(CACNA1F):c.5670+69C>T rs61653156 0.04931
NM_001256789.3(CACNA1F):c.3597+44T>G rs7886686 0.04281
NM_001256789.3(CACNA1F):c.3237-71G>C rs73498062 0.04138
NM_001256789.3(CACNA1F):c.2673+3G>A rs41312124 0.04106
NM_001256789.3(CACNA1F):c.2335-138G>A rs56114689 0.03905
NM_001256789.3(CACNA1F):c.3597+131T>C rs147150039 0.02827
NM_001256789.3(CACNA1F):c.1523G>A (p.Arg508Gln) rs34162630 0.01756
NM_001256789.3(CACNA1F):c.3742G>A (p.Ala1248Thr) rs34308720 0.00444
NM_001256789.3(CACNA1F):c.5048G>A (p.Gly1683Glu) rs147329320 0.00436
NM_001256789.3(CACNA1F):c.5829C>T (p.Asp1943=) rs138189763 0.00415
NM_001256789.3(CACNA1F):c.2733+15C>T rs199570194 0.00259
NM_001256789.3(CACNA1F):c.1870G>A (p.Val624Ile) rs141010716 0.00227
NM_001256789.3(CACNA1F):c.5700T>C (p.Phe1900=) rs143269092 0.00227
NM_001256789.3(CACNA1F):c.3651C>T (p.Val1217=) rs150205903 0.00216
NM_001256789.3(CACNA1F):c.3439-18C>T rs199764042 0.00179
NM_001256789.3(CACNA1F):c.885C>T (p.Asn295=) rs199749384 0.00107
NM_001256789.3(CACNA1F):c.5577C>T (p.Gly1859=) rs141521080 0.00088
NM_001256789.3(CACNA1F):c.827C>T (p.Ala276Val) rs184711457 0.00082
NM_001256789.3(CACNA1F):c.3930C>A (p.Ile1310=) rs144131971 0.00064
NM_001256789.3(CACNA1F):c.1435G>A (p.Gly479Arg) rs201059988 0.00063
NM_001256789.3(CACNA1F):c.1979C>G (p.Ser660Cys) rs143938580 0.00056
NM_001256789.3(CACNA1F):c.3741C>T (p.Asp1247=) rs199504022 0.00043
NM_001256789.3(CACNA1F):c.5763G>A (p.Thr1921=) rs190606884 0.00027
NM_001256789.3(CACNA1F):c.2635G>A (p.Ala879Thr) rs782464083 0.00014
NM_001256789.3(CACNA1F):c.5846C>T (p.Ser1949Phe) rs373041656 0.00013
NM_001256789.3(CACNA1F):c.3708+7C>T rs782716515 0.00011
NM_001256789.3(CACNA1F):c.90C>T (p.Pro30=) rs782095705 0.00009
NM_001256789.3(CACNA1F):c.1382C>T (p.Ala461Val) rs2272704 0.00006
NM_001256789.3(CACNA1F):c.1651+8C>G rs956287715 0.00002
NM_001256789.3(CACNA1F):c.5541C>T (p.Gly1847=) rs782486989 0.00002
NM_001256789.3(CACNA1F):c.1290C>T (p.Ala430=) rs782593082 0.00001
NM_001256789.3(CACNA1F):c.25+9A>G rs782719571 0.00001
NM_001256789.3(CACNA1F):c.1118+6=
NM_001256789.3(CACNA1F):c.1155C>T (p.Arg385=)
NM_001256789.3(CACNA1F):c.123G>A (p.Gly41=) rs35142387
NM_001256789.3(CACNA1F):c.1535G>A (p.Arg512His) rs146847449
NM_001256789.3(CACNA1F):c.1809= (p.Gly603=)
NM_001256789.3(CACNA1F):c.1809T>C (p.Gly603=) rs2235127
NM_001256789.3(CACNA1F):c.2289-202= rs2904024
NM_001256789.3(CACNA1F):c.2387-19del rs375791434
NM_001256789.3(CACNA1F):c.2387-27dup rs375791434
NM_001256789.3(CACNA1F):c.2391GGA[8] (p.Glu814dup) rs112450928
NM_001256789.3(CACNA1F):c.2674-20C>T rs376797886
NM_001256789.3(CACNA1F):c.3089+149dup rs11403487
NM_001256789.3(CACNA1F):c.3237-16C>G rs190434065
NM_001256789.3(CACNA1F):c.3237-16C>T rs190434065
NM_001256789.3(CACNA1F):c.3276= (p.His1092=)
NM_001256789.3(CACNA1F):c.3597+212dup rs139742315
NM_001256789.3(CACNA1F):c.382-15dup
NM_001256789.3(CACNA1F):c.3943-11dup
NM_001256789.3(CACNA1F):c.3943-17del rs781910822
NM_001256789.3(CACNA1F):c.4180G>A (p.Gly1394Ser) rs35212576
NM_001256789.3(CACNA1F):c.4467A>C (p.Pro1489=) rs199990102
NM_001256789.3(CACNA1F):c.5017G>T (p.Gly1673Trp) rs139409733

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