ClinVar Miner

List of variants in gene combination LOC126859837, SYNE1 reported by Revvity Omics, Revvity

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_182961.4(SYNE1):c.16850G>A (p.Arg5617Gln) rs141550859 0.00049
NM_182961.4(SYNE1):c.16831C>T (p.Arg5611Trp) rs369292604 0.00017
NM_182961.4(SYNE1):c.16901T>C (p.Met5634Thr) rs138509817 0.00012
NM_182961.4(SYNE1):c.17089C>T (p.Arg5697Trp) rs150290283 0.00010
NM_182961.4(SYNE1):c.17150A>C (p.Glu5717Ala) rs780396166 0.00008
NM_182961.4(SYNE1):c.16786G>A (p.Val5596Met) rs148158986 0.00007
NM_182961.4(SYNE1):c.17029T>C (p.Ser5677Pro) rs373679435 0.00003
NM_182961.4(SYNE1):c.17162G>A (p.Arg5721Gln) rs767936566 0.00003
NM_182961.4(SYNE1):c.17014C>T (p.Arg5672Trp) rs780794124 0.00002
NM_182961.4(SYNE1):c.17090G>A (p.Arg5697Gln) rs762894220 0.00002
NM_182961.4(SYNE1):c.17174C>A (p.Thr5725Asn) rs751747080 0.00002
NM_182961.4(SYNE1):c.16874A>C (p.Gln5625Pro) rs1273499044 0.00001
NM_182961.4(SYNE1):c.17015G>A (p.Arg5672Gln) rs886043150 0.00001
NM_182961.4(SYNE1):c.16828G>A (p.Gly5610Arg) rs2095522708
NM_182961.4(SYNE1):c.16834G>A (p.Glu5612Lys) rs2482799625
NM_182961.4(SYNE1):c.16984C>T (p.Arg5662Cys) rs145899734
NM_182961.4(SYNE1):c.16985G>C (p.Arg5662Pro) rs144895914
NM_182961.4(SYNE1):c.17051C>T (p.Pro5684Leu) rs754313756
NM_182961.4(SYNE1):c.17129A>G (p.His5710Arg) rs2482643245
NM_182961.4(SYNE1):c.17174C>T (p.Thr5725Ile) rs751747080
NM_182961.4(SYNE1):c.17176G>T (p.Ala5726Ser) rs775685010

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