ClinVar Miner

List of variants in gene SYNE1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 22
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HGVS dbSNP
NM_182961.4(SYNE1):c.11594C>T (p.Thr3865Met) rs202173395
NM_182961.4(SYNE1):c.15863G>C (p.Gly5288Ala) rs201313856
NM_182961.4(SYNE1):c.16229G>A (p.Arg5410Gln) rs776100963
NM_182961.4(SYNE1):c.16901T>C (p.Met5634Thr) rs138509817
NM_182961.4(SYNE1):c.1943G>A (p.Arg648Gln) rs768605521
NM_182961.4(SYNE1):c.1951C>T (p.Pro651Ser) rs1455678689
NM_182961.4(SYNE1):c.19544T>C (p.Phe6515Ser) rs747674900
NM_182961.4(SYNE1):c.20182C>T (p.Arg6728Cys) rs150063353
NM_182961.4(SYNE1):c.21815A>G (p.Lys7272Arg) rs764715827
NM_182961.4(SYNE1):c.23260G>A (p.Val7754Ile) rs150550013
NM_182961.4(SYNE1):c.245G>A (p.Arg82Gln) rs143900928
NM_182961.4(SYNE1):c.24723C>G (p.His8241Gln) rs141586001
NM_182961.4(SYNE1):c.25246+3G>A rs765849365
NM_182961.4(SYNE1):c.25706T>C (p.Ile8569Thr) rs760698113
NM_182961.4(SYNE1):c.25856T>C (p.Leu8619Pro) rs139834542
NM_182961.4(SYNE1):c.3404A>C (p.Glu1135Ala) rs764928878
NM_182961.4(SYNE1):c.3493C>T (p.Arg1165Cys) rs777507702
NM_182961.4(SYNE1):c.5269A>G (p.Ile1757Val) rs1196594228
NM_182961.4(SYNE1):c.8005-3C>T rs117084693
NM_182961.4(SYNE1):c.9148C>G (p.Leu3050Val) rs117360770
NM_182961.4(SYNE1):c.9377C>G (p.Ser3126Cys) rs139089832
NM_182961.4(SYNE1):c.9448G>A (p.Ala3150Thr) rs141821444

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