ClinVar Miner

List of variants in gene SYT14 reported by Ambry Genetics

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001146262.4(SYT14):c.202A>G (p.Arg68Gly) rs149170280 0.00042
NM_001146262.4(SYT14):c.398C>T (p.Ser133Leu) rs145963511 0.00019
NM_001146262.4(SYT14):c.8T>C (p.Ile3Thr) rs1351759000 0.00006
NM_001146262.4(SYT14):c.121C>T (p.Leu41Phe) rs188995220 0.00005
NM_001146262.4(SYT14):c.1709C>T (p.Ala570Val) rs970796538 0.00004
NM_001146262.4(SYT14):c.587A>G (p.Asn196Ser) rs200087065 0.00003
NM_001146262.4(SYT14):c.-5G>A rs749192802 0.00002
NM_001146262.4(SYT14):c.392C>G (p.Pro131Arg) rs1192775388 0.00002
NM_001146262.4(SYT14):c.551T>C (p.Ile184Thr) rs1027115343 0.00002
NM_001146262.4(SYT14):c.1493C>G (p.Pro498Arg) rs746278965 0.00001
NM_001146262.4(SYT14):c.274G>A (p.Glu92Lys) rs978216836 0.00001
NM_001146262.4(SYT14):c.1034T>G (p.Phe345Cys) rs2527943831
NM_001146262.4(SYT14):c.1054C>T (p.Arg352Cys) rs867886951
NM_001146262.4(SYT14):c.1123A>G (p.Met375Val)
NM_001146262.4(SYT14):c.1184G>A (p.Ser395Asn) rs752196611
NM_001146262.4(SYT14):c.1186G>A (p.Val396Met) rs192258059
NM_001146262.4(SYT14):c.1207G>C (p.Glu403Gln)
NM_001146262.4(SYT14):c.1239T>A (p.His413Gln) rs2083256885
NM_001146262.4(SYT14):c.1259T>G (p.Leu420Arg)
NM_001146262.4(SYT14):c.1301C>T (p.Ala434Val) rs2528232620
NM_001146262.4(SYT14):c.1315G>A (p.Gly439Ser) rs1375143721
NM_001146262.4(SYT14):c.134A>T (p.Tyr45Phe)
NM_001146262.4(SYT14):c.1366T>C (p.Cys456Arg) rs2528251650
NM_001146262.4(SYT14):c.1409G>A (p.Arg470Gln)
NM_001146262.4(SYT14):c.1564C>G (p.Leu522Val) rs2528260817
NM_001146262.4(SYT14):c.1582C>T (p.Arg528Cys)
NM_001146262.4(SYT14):c.1586G>T (p.Ser529Ile)
NM_001146262.4(SYT14):c.160A>G (p.Asn54Asp)
NM_001146262.4(SYT14):c.238A>C (p.Met80Leu)
NM_001146262.4(SYT14):c.36A>G (p.Val12=)
NM_001146262.4(SYT14):c.400G>A (p.Ala134Thr)
NM_001146262.4(SYT14):c.436G>A (p.Asp146Asn)
NM_001146262.4(SYT14):c.446A>G (p.Asn149Ser) rs2527907597
NM_001146262.4(SYT14):c.539C>T (p.Thr180Ile)
NM_001146262.4(SYT14):c.554G>A (p.Gly185Glu)
NM_001146262.4(SYT14):c.656A>C (p.His219Pro)
NM_001146262.4(SYT14):c.743A>T (p.Gln248Leu)
NM_001146262.4(SYT14):c.773A>T (p.Glu258Val)
NM_001146262.4(SYT14):c.94G>C (p.Val32Leu)

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