List of variants in gene SYNE1 reported as uncertain significance by Baylor Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 41

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.4107T>A (p.Phe1369Leu)	rs149109801	0.00172
NM_182961.4(SYNE1):c.6339T>C (p.Thr2113=)	rs141671123	0.00106
NM_182961.4(SYNE1):c.14452T>A (p.Tyr4818Asn)	rs142422990	0.00101
NM_182961.4(SYNE1):c.21995A>C (p.His7332Pro)	rs151247098	0.00080
NM_182961.4(SYNE1):c.3536A>C (p.Glu1179Ala)	rs117461489	0.00057
NM_182961.4(SYNE1):c.25342G>A (p.Asp8448Asn)	rs139679692	0.00016
NM_182961.4(SYNE1):c.10078C>A (p.Gln3360Lys)	rs774710219	0.00014
NM_182961.4(SYNE1):c.22783A>G (p.Ile7595Val)	rs146320179	0.00014
NM_182961.4(SYNE1):c.16552C>T (p.Arg5518Trp)	rs377410590	0.00008
NM_182961.4(SYNE1):c.334A>T (p.Thr112Ser)	rs750010888	0.00006
NM_182961.4(SYNE1):c.22519C>T (p.Arg7507Cys)	rs141278167	0.00005
NM_182961.4(SYNE1):c.1453A>G (p.Met485Val)	rs767978898	0.00004
NM_182961.4(SYNE1):c.22520G>A (p.Arg7507His)	rs776733924	0.00004
NM_182961.4(SYNE1):c.5417A>G (p.His1806Arg)	rs779891217	0.00004
NM_182961.4(SYNE1):c.10284G>T (p.Met3428Ile)	rs755180412	0.00003
NM_182961.4(SYNE1):c.10766C>T (p.Thr3589Ile)	rs201487756	0.00003
NM_182961.4(SYNE1):c.13918T>C (p.Tyr4640His)	rs748256440	0.00003
NM_182961.4(SYNE1):c.241C>T (p.Arg81Cys)	rs375917264	0.00003
NM_182961.4(SYNE1):c.11002G>A (p.Glu3668Lys)	rs767544504	0.00002
NM_182961.4(SYNE1):c.24354C>G (p.Asp8118Glu)	rs149940427	0.00002
NM_182961.4(SYNE1):c.14634A>C (p.Glu4878Asp)	rs1159750019	0.00001
NM_182961.4(SYNE1):c.20821A>G (p.Ile6941Val)	rs191912037	0.00001
NM_182961.4(SYNE1):c.21077A>C (p.Glu7026Ala)	rs777755452	0.00001
NM_182961.4(SYNE1):c.23936G>A (p.Arg7979Gln)	rs769773495	0.00001
NM_182961.4(SYNE1):c.3506A>T (p.Glu1169Val)	rs750101869	0.00001
NM_182961.4(SYNE1):c.508C>T (p.Arg170Trp)	rs777175001	0.00001
NM_182961.4(SYNE1):c.8984T>C (p.Ile2995Thr)	rs527822279	0.00001
NM_182961.4(SYNE1):c.10112C>T (p.Ala3371Val)	rs748579024
NM_182961.4(SYNE1):c.12066C>G (p.Ser4022Arg)
NM_182961.4(SYNE1):c.12955A>C (p.Ser4319Arg)	rs1267678977
NM_182961.4(SYNE1):c.18409G>A (p.Val6137Met)	rs945540285
NM_182961.4(SYNE1):c.20136C>G (p.Ile6712Met)	rs761906590
NM_182961.4(SYNE1):c.21195+14G>C	rs2082553069
NM_182961.4(SYNE1):c.25523A>G (p.Glu8508Gly)	rs2057176996
NM_182961.4(SYNE1):c.5728A>G (p.Asn1910Asp)	rs1459660658
NM_182961.4(SYNE1):c.5980A>G (p.Ile1994Val)	rs2098156852
NM_182961.4(SYNE1):c.6128A>T (p.Lys2043Met)	rs1015453687
NM_182961.4(SYNE1):c.6412A>G (p.Lys2138Glu)	rs2097962380
NM_182961.4(SYNE1):c.8882A>G (p.Gln2961Arg)	rs1366579684
NM_182961.4(SYNE1):c.9220A>G (p.Arg3074Gly)	rs2097283597
NM_182961.4(SYNE1):c.9821G>A (p.Arg3274Lys)	rs2097100149

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