ClinVar Miner

List of variants in gene SYNE1 reported as likely benign for not provided

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Gene type:
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Total variants: 41
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HGVS dbSNP
NM_033071.3(SYNE1):c.10058C>A (p.Ser3353Tyr) rs150170988
NM_033071.3(SYNE1):c.1059T>C (p.Asp353=) rs144105769
NM_033071.3(SYNE1):c.11385G>A (p.Thr3795=) rs137919524
NM_033071.3(SYNE1):c.11440A>G (p.Thr3814Ala) rs115786671
NM_033071.3(SYNE1):c.11957C>T (p.Pro3986Leu) rs150179494
NM_033071.3(SYNE1):c.12012+4G>A rs770448083
NM_033071.3(SYNE1):c.13423G>A (p.Val4475Ile) rs4870093
NM_033071.3(SYNE1):c.13878G>T (p.Met4626Ile) rs141141950
NM_033071.3(SYNE1):c.17427C>T (p.Arg5809=) rs144418713
NM_033071.3(SYNE1):c.17584G>A (p.Ala5862Thr) rs113962905
NM_033071.3(SYNE1):c.1899A>G (p.Gln633=) rs62427038
NM_033071.3(SYNE1):c.19295A>G (p.Asn6432Ser) rs144762960
NM_033071.3(SYNE1):c.1985A>G (p.Gln662Arg) rs9397509
NM_033071.3(SYNE1):c.19950C>T (p.Asn6650=) rs201221147
NM_033071.3(SYNE1):c.21738C>T (p.Ser7246=) rs368864479
NM_033071.3(SYNE1):c.22926T>C (p.Arg7642=)
NM_033071.3(SYNE1):c.23102G>A (p.Arg7701Gln) rs138787771
NM_033071.3(SYNE1):c.25962G>A (p.Lys8654=) rs765865910
NM_033071.3(SYNE1):c.3108T>C (p.Asn1036=) rs770801617
NM_033071.3(SYNE1):c.3209T>C (p.Val1070Ala) rs141464488
NM_033071.3(SYNE1):c.3911C>T (p.Ala1304Val) rs35378260
NM_033071.3(SYNE1):c.4183C>T (p.Arg1395Trp) rs34028822
NM_033071.3(SYNE1):c.5091C>G (p.Val1697=) rs146789107
NM_033071.3(SYNE1):c.5122G>T (p.Ala1708Ser) rs149758808
NM_033071.3(SYNE1):c.5280T>C (p.Ile1760=) rs147508177
NM_033071.3(SYNE1):c.6020G>A (p.Arg2007Lys) rs149146258
NM_033071.3(SYNE1):c.6156T>G (p.Ile2052Met) rs116600265
NM_033071.3(SYNE1):c.6360T>C (p.Thr2120=) rs141671123
NM_033071.3(SYNE1):c.6669C>T (p.Cys2223=) rs185829704
NM_033071.3(SYNE1):c.687G>A (p.Pro229=) rs141368652
NM_033071.3(SYNE1):c.6910G>A (p.Gly2304Arg) rs117184249
NM_033071.3(SYNE1):c.6955T>C (p.Phe2319Leu) rs138004884
NM_033071.3(SYNE1):c.7479A>G (p.Gln2493=) rs139070088
NM_033071.3(SYNE1):c.8185G>A (p.Val2729Ile) rs151091241
NM_033071.3(SYNE1):c.9169C>G (p.Leu3057Val) rs117360770
NM_182961.3(SYNE1):c.11001C>T (p.Asp3667=)
NM_182961.3(SYNE1):c.11756C>T (p.Ala3919Val) rs114367594
NM_182961.3(SYNE1):c.297C>T (p.Leu99=)
NM_182961.3(SYNE1):c.462C>T (p.Ser154=)
NM_182961.3(SYNE1):c.8562T>C (p.Asp2854=)
NM_182961.3(SYNE1):c.8844C>T (p.Val2948=)

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