ClinVar Miner

List of variants in gene SYNJ1 reported as uncertain significance for Parkinson disease

Included ClinVar conditions (32):
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Gene type:
ClinVar version:
Total variants: 123
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HGVS dbSNP
NM_003895.3(SYNJ1):c.1047G>A (p.Met349Ile)
NM_003895.3(SYNJ1):c.1223G>A (p.Ser408Asn)
NM_003895.3(SYNJ1):c.137T>A (p.Phe46Tyr)
NM_003895.3(SYNJ1):c.142A>G (p.Ile48Val)
NM_003895.3(SYNJ1):c.1583T>C (p.Leu528Ser) rs1238065971
NM_003895.3(SYNJ1):c.158A>G (p.Asp53Gly)
NM_003895.3(SYNJ1):c.1625G>A (p.Arg542His)
NM_003895.3(SYNJ1):c.1672A>G (p.Ser558Gly) rs148901211
NM_003895.3(SYNJ1):c.1720G>A (p.Val574Ile)
NM_003895.3(SYNJ1):c.2023G>A (p.Val675Ile) rs373820739
NM_003895.3(SYNJ1):c.2050_2051delinsAG (p.Gln684Arg) rs1555896707
NM_003895.3(SYNJ1):c.2237T>C (p.Ile746Thr) rs147929290
NM_003895.3(SYNJ1):c.2288A>G (p.Tyr763Cys)
NM_003895.3(SYNJ1):c.2371G>T (p.Asp791Tyr)
NM_003895.3(SYNJ1):c.2495A>G (p.Tyr832Cys) rs1283151166
NM_003895.3(SYNJ1):c.2579-10C>G rs775703634
NM_003895.3(SYNJ1):c.2595_2597delTCT rs769856515
NM_003895.3(SYNJ1):c.2770G>A (p.Val924Ile)
NM_003895.3(SYNJ1):c.2861T>C (p.Ile954Thr)
NM_003895.3(SYNJ1):c.2898A>G (p.Glu966=) rs1350091132
NM_003895.3(SYNJ1):c.2991+5G>A rs371765751
NM_003895.3(SYNJ1):c.2991+6G>A
NM_003895.3(SYNJ1):c.3174T>G (p.Ser1058Arg)
NM_003895.3(SYNJ1):c.3214T>C (p.Ser1072Pro)
NM_003895.3(SYNJ1):c.3256C>G (p.Arg1086Gly)
NM_003895.3(SYNJ1):c.328G>C (p.Gly110Arg) rs1569113660
NM_003895.3(SYNJ1):c.3332C>A (p.Pro1111Gln)
NM_003895.3(SYNJ1):c.3398_3403del (p.Leu1133_Pro1134del) rs1283379982
NM_003895.3(SYNJ1):c.3421C>T (p.Pro1141Ser) rs1368672974
NM_003895.3(SYNJ1):c.3437G>A (p.Arg1146Gln)
NM_003895.3(SYNJ1):c.3548G>A (p.Gly1183Asp) rs142964720
NM_003895.3(SYNJ1):c.3671G>A (p.Gly1224Asp) rs1569030684
NM_003895.3(SYNJ1):c.3697G>C (p.Ala1233Pro) rs77164494
NM_003895.3(SYNJ1):c.3704C>A (p.Pro1235Gln)
NM_003895.3(SYNJ1):c.3704C>T (p.Pro1235Leu)
NM_003895.3(SYNJ1):c.3718C>T (p.Arg1240Cys) rs114994257
NM_003895.3(SYNJ1):c.3727G>A (p.Val1243Ile) rs1569027714
NM_003895.3(SYNJ1):c.3755G>A (p.Arg1252Gln) rs144048853
NM_003895.3(SYNJ1):c.3863C>T (p.Pro1288Leu)
NM_003895.3(SYNJ1):c.3884C>T (p.Pro1295Leu)
NM_003895.3(SYNJ1):c.3914C>G (p.Pro1305Arg)
NM_003895.3(SYNJ1):c.3928A>G (p.Met1310Val) rs751069566
NM_003895.3(SYNJ1):c.3999T>G (p.His1333Gln) rs1569025711
NM_003895.3(SYNJ1):c.4241C>T (p.Thr1414Ile)
NM_003895.3(SYNJ1):c.4642A>G (p.Ser1548Gly)
NM_003895.3(SYNJ1):c.51_62del (p.15_18GGCG[1]) rs1035093736
NM_003895.3(SYNJ1):c.587G>C (p.Arg196Thr)
NM_003895.3(SYNJ1):c.747A>T (p.Glu249Asp) rs1377390036
NM_003895.3(SYNJ1):c.920G>A (p.Arg307His)
NM_203446.2(SYNJ1):c.*127G>C
NM_203446.2(SYNJ1):c.*173C>T rs1341548536
NM_203446.2(SYNJ1):c.*188T>C rs866258846
NM_203446.2(SYNJ1):c.*233G>A
NM_203446.2(SYNJ1):c.*253A>G
NM_203446.2(SYNJ1):c.*257G>T
NM_203446.2(SYNJ1):c.*316del rs1569014970
NM_203446.2(SYNJ1):c.*491A>C
NM_203446.2(SYNJ1):c.*521C>G rs749527882
NM_203446.2(SYNJ1):c.*574T>A rs138122167
NM_203446.2(SYNJ1):c.*666A>G
NM_203446.2(SYNJ1):c.*678C>G
NM_203446.2(SYNJ1):c.*767T>G
NM_203446.2(SYNJ1):c.1121A>C (p.Tyr374Ser)
NM_203446.2(SYNJ1):c.1408G>A (p.Val470Met)
NM_203446.2(SYNJ1):c.1423A>G (p.Ile475Val) rs763870801
NM_203446.2(SYNJ1):c.1566T>G (p.Asn522Lys)
NM_203446.2(SYNJ1):c.1598G>A (p.Arg533Gln) rs781599934
NM_203446.2(SYNJ1):c.1624C>T (p.Arg542Cys)
NM_203446.2(SYNJ1):c.1671G>C (p.Lys557Asn)
NM_203446.2(SYNJ1):c.1726G>A (p.Val576Ile) rs1555898799
NM_203446.2(SYNJ1):c.1906G>A (p.Ala636Thr)
NM_203446.2(SYNJ1):c.1949G>T (p.Trp650Leu) rs1481650772
NM_203446.2(SYNJ1):c.2207T>C (p.Val736Ala)
NM_203446.2(SYNJ1):c.2367T>A (p.Asn789Lys)
NM_203446.2(SYNJ1):c.2579-6C>A
NM_203446.2(SYNJ1):c.2636C>T (p.Thr879Met)
NM_203446.2(SYNJ1):c.2684C>A (p.Thr895Asn)
NM_203446.2(SYNJ1):c.2714T>C (p.Ile905Thr) rs114053718
NM_203446.2(SYNJ1):c.2721A>G (p.Ile907Met) rs377165480
NM_203446.2(SYNJ1):c.2748G>C (p.Glu916Asp) rs375526059
NM_203446.2(SYNJ1):c.2802A>G (p.Thr934=)
NM_203446.2(SYNJ1):c.2903T>C (p.Ile968Thr) rs755258923
NM_203446.2(SYNJ1):c.2909T>C (p.Ile970Thr) rs932390799
NM_203446.2(SYNJ1):c.294A>G (p.Ala98=)
NM_203446.2(SYNJ1):c.2999A>G (p.Asn1000Ser) rs754401787
NM_203446.2(SYNJ1):c.3001C>T (p.Arg1001Trp)
NM_203446.2(SYNJ1):c.3013A>G (p.Ile1005Val)
NM_203446.2(SYNJ1):c.3071A>G (p.Lys1024Arg)
NM_203446.2(SYNJ1):c.3098C>A (p.Thr1033Lys)
NM_203446.2(SYNJ1):c.3113T>A (p.Leu1038His)
NM_203446.2(SYNJ1):c.316C>T (p.Arg106Trp) rs372488661
NM_203446.2(SYNJ1):c.317G>A (p.Arg106Gln)
NM_203446.2(SYNJ1):c.3296C>G (p.Pro1099Arg) rs1430500307
NM_203446.2(SYNJ1):c.32G>A (p.Ser11Asn)
NM_203446.2(SYNJ1):c.3326G>A (p.Arg1109Gln) rs141107054
NM_203446.2(SYNJ1):c.3407A>G (p.Lys1136Arg) rs946267411
NM_203446.2(SYNJ1):c.3493C>A (p.Pro1165Thr)
NM_203446.2(SYNJ1):c.3509-5A>G
NM_203446.2(SYNJ1):c.3527C>T (p.Pro1176Leu) rs569046864
NM_203446.2(SYNJ1):c.3548-8C>A
NM_203446.2(SYNJ1):c.3641G>C (p.Ser1214Thr) rs994115947
NM_203446.2(SYNJ1):c.3698C>G (p.Ala1233Gly)
NM_203446.2(SYNJ1):c.3705G>A (p.Pro1235=) rs1160685381
NM_203446.2(SYNJ1):c.3751G>A (p.Ala1251Thr)
NM_203446.2(SYNJ1):c.3769A>G (p.Arg1257Gly)
NM_203446.2(SYNJ1):c.3806C>T (p.Thr1269Met) rs752805765
NM_203446.2(SYNJ1):c.3808T>C (p.Ser1270Pro) rs767695759
NM_203446.2(SYNJ1):c.3839T>C (p.Leu1280Pro) rs548516848
NM_203446.2(SYNJ1):c.3920C>T (p.Ala1307Val)
NM_203446.2(SYNJ1):c.3940G>A (p.Gly1314Ser)
NM_203446.2(SYNJ1):c.3946dup (p.Gln1316fs) rs1555888341
NM_203446.2(SYNJ1):c.3954T>A (p.Asn1318Lys) rs1555888329
NM_203446.2(SYNJ1):c.4025A>G (p.Gln1342Arg) rs546986773
NM_203446.2(SYNJ1):c.428T>C (p.Ile143Thr) rs779426150
NM_203446.2(SYNJ1):c.443A>T (p.Asp148Val)
NM_203446.2(SYNJ1):c.700G>A (p.Ala234Thr)
NM_203446.2(SYNJ1):c.739A>G (p.Ser247Gly)
NM_203446.2(SYNJ1):c.76A>G (p.Arg26Gly) rs988950141
NM_203446.2(SYNJ1):c.7A>C (p.Lys3Gln)
NM_203446.2(SYNJ1):c.885C>G (p.Phe295Leu)
NM_203446.2(SYNJ1):c.925C>T (p.Arg309Cys) rs547450707
NM_203446.2(SYNJ1):c.926G>A (p.Arg309His) rs532075408
NM_203446.2(SYNJ1):c.959C>G (p.Ala320Gly) rs1046699971

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