ClinVar Miner

List of variants in gene SYNJ1 reported as likely benign for not provided

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_203446.3(SYNJ1):c.3588+128G>A rs56238975 0.03292
NM_203446.3(SYNJ1):c.125-148A>C rs74625247 0.02895
NM_203446.3(SYNJ1):c.3392-96T>A rs34001349 0.01811
NM_203446.3(SYNJ1):c.851+43A>G rs73194279 0.01622
NM_203446.3(SYNJ1):c.3038-289A>G rs74845933 0.01574
NM_203446.3(SYNJ1):c.3916-135A>G rs114017370 0.01383
NM_203446.3(SYNJ1):c.211+169C>A rs114291633 0.01380
NM_203446.3(SYNJ1):c.3589-121T>C rs144067694 0.01339
NM_203446.3(SYNJ1):c.1811+51A>G rs114386610 0.01281
NM_203446.3(SYNJ1):c.1353+27C>T rs80299581 0.01048
NM_203446.3(SYNJ1):c.790-49G>A rs116477798 0.01022
NM_203446.3(SYNJ1):c.1511-320T>C rs146920389 0.00887
NM_203446.3(SYNJ1):c.*3+277T>C rs147290377 0.00809
NM_203446.3(SYNJ1):c.1726+155A>G rs148576574 0.00719
NM_203446.3(SYNJ1):c.1811+266T>A rs115927760 0.00614
NM_203446.3(SYNJ1):c.*611C>T rs76056543 0.00609
NM_203446.3(SYNJ1):c.1511-164C>T rs78594462 0.00576
NM_203446.3(SYNJ1):c.3915+247G>A rs546596367 0.00556
NM_203446.3(SYNJ1):c.1535-142G>A rs151097134 0.00475
NM_203446.3(SYNJ1):c.479+150G>A rs141549722 0.00466
NM_203446.3(SYNJ1):c.6G>A (p.Ala2=) rs61750221 0.00452
NM_203446.3(SYNJ1):c.43C>T (p.Pro15Ser) rs61755328 0.00441
NM_203446.3(SYNJ1):c.3589-264T>C rs79525135 0.00438
NM_203446.3(SYNJ1):c.573A>G (p.Thr191=) rs61756694 0.00406
NM_203446.3(SYNJ1):c.2796-129C>T rs144426013 0.00354
NM_203446.3(SYNJ1):c.*728C>T rs2230767 0.00284
NM_203446.3(SYNJ1):c.2304+55C>T rs566112543 0.00272
NM_203446.3(SYNJ1):c.1030G>A (p.Ala344Thr) rs114942253 0.00255
NM_203446.3(SYNJ1):c.3698-251G>C rs147026277 0.00254
NM_203446.3(SYNJ1):c.2943G>T (p.Met981Ile) rs115683257 0.00245
NM_203446.3(SYNJ1):c.*315G>A rs145347648 0.00241
NM_203446.3(SYNJ1):c.3590C>T (p.Thr1197Met) rs145937537 0.00200
NM_203446.3(SYNJ1):c.3369A>G (p.Pro1123=) rs368850131 0.00183
NM_203446.3(SYNJ1):c.*4G>A rs115648918 0.00158
NM_203446.3(SYNJ1):c.2346G>A (p.Pro782=) rs61753644 0.00088
NM_203446.3(SYNJ1):c.2120T>C (p.Ile707Thr) rs147929290 0.00074
NM_203446.3(SYNJ1):c.*732C>T rs148676465 0.00068
NM_203446.3(SYNJ1):c.*552G>A rs146425050 0.00064
NM_203446.3(SYNJ1):c.909A>G (p.Gly303=) rs145522240 0.00026
NM_203446.3(SYNJ1):c.2874+5G>A rs371765751 0.00024
NM_203446.3(SYNJ1):c.3753T>G (p.Ser1251=) rs150595970 0.00012
NM_203446.3(SYNJ1):c.3762C>T (p.Pro1254=) rs201117151 0.00009
NM_203446.3(SYNJ1):c.-31G>C rs751083536 0.00006
NM_203446.3(SYNJ1):c.*690G>A rs559102258 0.00005
NM_203446.3(SYNJ1):c.2172T>C (p.Tyr724=) rs144454116 0.00005
NM_203446.3(SYNJ1):c.1511-4A>G rs533995497 0.00003
NM_203446.3(SYNJ1):c.324C>T (p.Ile108=) rs551070196 0.00003
NM_203446.3(SYNJ1):c.-49A>G rs780877494 0.00002
NM_203446.3(SYNJ1):c.1959T>G (p.Val653=) rs747138067 0.00002
NM_203446.3(SYNJ1):c.*75A>G rs756090874 0.00001
NM_203446.3(SYNJ1):c.3270A>G (p.Pro1090=) rs1299635688 0.00001
NM_203446.3(SYNJ1):c.3324G>A (p.Pro1108=) rs757804939 0.00001
NM_203446.3(SYNJ1):c.885A>G (p.Lys295=) rs1219063833 0.00001
NM_203446.3(SYNJ1):c.*487C>T
NM_203446.3(SYNJ1):c.*522G>C rs777945782
NM_203446.3(SYNJ1):c.*801A>G
NM_203446.3(SYNJ1):c.1535-202del rs931173780
NM_203446.3(SYNJ1):c.1535-202dup rs931173780
NM_203446.3(SYNJ1):c.212-210G>A rs147026419
NM_203446.3(SYNJ1):c.2131T>C (p.Leu711=)
NM_203446.3(SYNJ1):c.2259T>C (p.Ser753=) rs1601341192
NM_203446.3(SYNJ1):c.294T>C (p.Val98=) rs1601468711
NM_203446.3(SYNJ1):c.3009A>C (p.Ala1003=)
NM_203446.3(SYNJ1):c.309T>C (p.Phe103=) rs1569111289
NM_203446.3(SYNJ1):c.3126C>A (p.Pro1042=) rs1601264866
NM_203446.3(SYNJ1):c.3264G>T (p.Ala1088=) rs1601260544
NM_203446.3(SYNJ1):c.3300C>T (p.Ala1100=) rs2040034208
NM_203446.3(SYNJ1):c.3392-202_3392-199del rs142688189
NM_203446.3(SYNJ1):c.3479-29T>G rs146753923
NM_203446.3(SYNJ1):c.384T>C (p.Phe128=) rs746811167
NM_203446.3(SYNJ1):c.3915+153AT[8] rs112225294
NM_203446.3(SYNJ1):c.504C>T (p.Leu168=) rs1601450035
NM_203446.3(SYNJ1):c.706-209T>G rs116699197
NM_203446.3(SYNJ1):c.852-6A>G rs1601422344

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