ClinVar Miner

List of variants in gene SYN1 reported by Ambry Genetics

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_006950.3(SYN1):c.510T>C (p.Asn170=) rs1142636 0.39391
NM_006950.3(SYN1):c.1699A>G (p.Thr567Ala) rs200533370 0.01462
NM_006950.3(SYN1):c.912C>T (p.Ala304=) rs62636605 0.01433
NM_006950.3(SYN1):c.152C>G (p.Ala51Gly) rs187134574 0.01317
NM_006950.3(SYN1):c.1107C>T (p.Ile369=) rs150248483 0.00107
NM_006950.3(SYN1):c.1110C>T (p.Cys370=) rs141925310 0.00101
NM_006950.3(SYN1):c.1325T>C (p.Leu442Pro) rs375440874 0.00058
NM_006950.3(SYN1):c.1615G>A (p.Gly539Ser) rs794727076 0.00058
NM_006950.3(SYN1):c.426A>G (p.Lys142=) rs145911562 0.00054
NM_006950.3(SYN1):c.1701A>T (p.Thr567=) rs770195822 0.00046
NM_006950.3(SYN1):c.1063C>T (p.Leu355=) rs191822319 0.00025
NM_006950.3(SYN1):c.1569G>A (p.Ala523=) rs587781185 0.00022
NM_006950.3(SYN1):c.939C>T (p.Asp313=) rs373928763 0.00020
NM_006950.3(SYN1):c.1968G>A (p.Pro656=) rs199844514 0.00018
NM_006950.3(SYN1):c.319G>A (p.Gly107Ser) rs765045862 0.00012
NM_006950.3(SYN1):c.1372C>G (p.Gln458Glu) rs372445055 0.00011
NM_006950.3(SYN1):c.526C>T (p.Arg176Trp) rs769458536 0.00010
NM_006950.3(SYN1):c.1026G>A (p.Ala342=) rs777301855 0.00005
NM_006950.3(SYN1):c.108T>C (p.Gly36=) rs758180955 0.00005
NM_006950.3(SYN1):c.1321G>T (p.Ala441Ser) rs772106134 0.00004
NM_006950.3(SYN1):c.371C>T (p.Thr124Ile) rs1339768860 0.00004
NM_006950.3(SYN1):c.585C>T (p.Asn195=) rs746025499 0.00003
NM_006950.3(SYN1):c.505C>T (p.Arg169Trp) rs762284940 0.00002
NM_006950.3(SYN1):c.1076C>A (p.Thr359Lys) rs765183335 0.00001
NM_006950.3(SYN1):c.1198G>A (p.Asp400Asn) rs772668988 0.00001
NM_006950.3(SYN1):c.1657T>C (p.Ser553Pro) rs1165799072 0.00001
NM_006950.3(SYN1):c.1818G>A (p.Gln606=) rs967215240 0.00001
NM_006950.3(SYN1):c.1967C>T (p.Pro656Leu) rs1391622247 0.00001
NM_006950.3(SYN1):c.112_126del (p.His38_Ala42del) rs2057941937
NM_006950.3(SYN1):c.1169C>A (p.Ser390Tyr) rs1569322942
NM_006950.3(SYN1):c.1310del (p.Pro437fs) rs1569322834
NM_006950.3(SYN1):c.1321G>A (p.Ala441Thr) rs772106134
NM_006950.3(SYN1):c.1322C>A (p.Ala441Asp) rs1569322817
NM_006950.3(SYN1):c.1324C>T (p.Leu442=)
NM_006950.3(SYN1):c.1460C>T (p.Pro487Leu) rs2147912337
NM_006950.3(SYN1):c.1481C>T (p.Ser494Leu)
NM_006950.3(SYN1):c.1660C>T (p.Pro554Ser)
NM_006950.3(SYN1):c.169G>A (p.Val57Ile) rs1200321961
NM_006950.3(SYN1):c.1704C>G (p.Ser568=)
NM_006950.3(SYN1):c.1711G>A (p.Gly571Ser) rs1284009431
NM_006950.3(SYN1):c.1721C>T (p.Pro574Leu)
NM_006950.3(SYN1):c.1831C>T (p.Pro611Ser) rs1300239224
NM_006950.3(SYN1):c.187C>G (p.Pro63Ala)
NM_006950.3(SYN1):c.189G>A (p.Pro63=) rs371739376
NM_006950.3(SYN1):c.189G>T (p.Pro63=) rs371739376
NM_006950.3(SYN1):c.1970A>C (p.His657Pro) rs992542097
NM_006950.3(SYN1):c.402G>T (p.Lys134Asn)
NM_006950.3(SYN1):c.425A>T (p.Lys142Ile)
NM_006950.3(SYN1):c.485C>T (p.Ser162Phe)
NM_006950.3(SYN1):c.635G>T (p.Ser212Ile) rs1556860638
NM_006950.3(SYN1):c.668G>C (p.Cys223Ser) rs796053398
NM_006950.3(SYN1):c.712A>G (p.Lys238Glu)
NM_006950.3(SYN1):c.885G>A (p.Val295=)

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