ClinVar Miner

List of variants in gene SLC6A8 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_005629.4(SLC6A8):c.1496-5C>T rs200695210 0.00491
NM_005629.4(SLC6A8):c.1768-3C>T rs150207268 0.00435
NM_005629.4(SLC6A8):c.1141+18G>A rs187400676 0.00362
NM_005629.4(SLC6A8):c.1494C>T (p.Tyr498=) rs143916832 0.00249
NM_005629.4(SLC6A8):c.813C>T (p.Val271=) rs138064933 0.00248
NM_005629.4(SLC6A8):c.780C>T (p.Ile260=) rs148232368 0.00177
NM_005629.4(SLC6A8):c.603C>T (p.Asp201=) rs143019641 0.00073
NM_005629.4(SLC6A8):c.777+4C>T rs201581661 0.00063
NM_005629.4(SLC6A8):c.1626C>T (p.Tyr542=) rs140601882 0.00042
NM_005629.4(SLC6A8):c.1516G>A (p.Asp506Asn) rs201526436 0.00036
NM_005629.4(SLC6A8):c.1649C>G (p.Thr550Ser) rs199635059 0.00033
NM_005629.4(SLC6A8):c.1162G>A (p.Ala388Thr) rs374163604 0.00032
NM_005629.4(SLC6A8):c.544G>A (p.Val182Met) rs149024147 0.00032
NM_005629.4(SLC6A8):c.1020C>T (p.Asp340=) rs144252036 0.00024
NM_005629.4(SLC6A8):c.1778A>G (p.His593Arg) rs782560726 0.00024
NM_005629.4(SLC6A8):c.1890G>C (p.Val630=) rs376385129 0.00023
NM_005629.4(SLC6A8):c.819C>T (p.Val273=) rs143750068 0.00021
NM_005629.4(SLC6A8):c.645-6C>T rs377181706 0.00016
NM_005629.4(SLC6A8):c.1281C>T (p.Thr427=) rs368950125 0.00013
NM_005629.4(SLC6A8):c.1473C>T (p.Cys491=) rs122453118 0.00013
NM_005629.4(SLC6A8):c.1533C>T (p.Ile511=) rs782114947 0.00011
NM_005629.4(SLC6A8):c.826C>T (p.Leu276=) rs138634140 0.00011
NM_005629.4(SLC6A8):c.87G>C (p.Gly29=) rs782373793 0.00011
NM_005629.4(SLC6A8):c.92C>T (p.Pro31Leu) rs868950793 0.00011
NM_005629.4(SLC6A8):c.1496-4G>A rs782589547 0.00010
NM_005629.4(SLC6A8):c.1570T>A (p.Ser524Thr) rs782703394 0.00010
NM_005629.4(SLC6A8):c.1662G>A (p.Pro554=) rs149677083 0.00010
NM_005629.4(SLC6A8):c.1141+6G>A rs373124777 0.00009
NM_005629.4(SLC6A8):c.1452C>G (p.Leu484=) rs376421364 0.00009
NM_005629.4(SLC6A8):c.912+15G>A rs1456582785 0.00009
NM_005629.4(SLC6A8):c.1497A>G (p.Gly499=) rs199640501 0.00008
NM_005629.4(SLC6A8):c.1810T>A (p.Leu604Met) rs1301772452 0.00008
NM_005629.4(SLC6A8):c.1830C>T (p.Asp610=) rs1803330 0.00008
NM_005629.4(SLC6A8):c.1038C>T (p.Leu346=) rs369716393 0.00006
NM_005629.4(SLC6A8):c.1113C>T (p.Gly371=) rs1411836045 0.00006
NM_005629.4(SLC6A8):c.126A>G (p.Thr42=) rs1557043825 0.00006
NM_005629.4(SLC6A8):c.1504C>T (p.Arg502Cys) rs782488606 0.00006
NM_005629.4(SLC6A8):c.1506C>T (p.Arg502=) rs782374700 0.00005
NM_005629.4(SLC6A8):c.1597-5C>T rs376073223 0.00005
NM_005629.4(SLC6A8):c.1646A>C (p.Asn549Thr) rs782790088 0.00005
NM_005629.4(SLC6A8):c.1713C>T (p.Cys571=) rs782244505 0.00005
NM_005629.4(SLC6A8):c.1884C>T (p.Val628=) rs782808736 0.00005
NM_005629.4(SLC6A8):c.498G>A (p.Thr166=) rs201260657 0.00005
NM_005629.4(SLC6A8):c.820G>A (p.Val274Met) rs782208622 0.00005
NM_005629.4(SLC6A8):c.1313A>T (p.Tyr438Phe) rs1403716189 0.00004
NM_005629.4(SLC6A8):c.1885G>A (p.Val629Ile) rs781899045 0.00004
NM_005629.4(SLC6A8):c.975A>C (p.Thr325=) rs782517934 0.00004
NM_005629.4(SLC6A8):c.1869C>T (p.Ser623=) rs782748657 0.00003
NM_005629.4(SLC6A8):c.234C>T (p.Phe78=) rs1229187797 0.00003
NM_005629.4(SLC6A8):c.1284C>T (p.Gly428=) rs781788160 0.00002
NM_005629.4(SLC6A8):c.1395C>T (p.Gly465=) rs782302903 0.00002
NM_005629.4(SLC6A8):c.1614C>T (p.Asn538=) rs369726574 0.00002
NM_005629.4(SLC6A8):c.1698G>C (p.Leu566=) rs782287646 0.00002
NM_005629.4(SLC6A8):c.1731G>A (p.Leu577=) rs1603217844 0.00002
NM_005629.4(SLC6A8):c.1831G>A (p.Ala611Thr) rs146949376 0.00002
NM_005629.4(SLC6A8):c.537C>T (p.Pro179=) rs202136567 0.00002
NM_005629.4(SLC6A8):c.76G>A (p.Gly26Arg) rs1233444890 0.00002
NM_005629.4(SLC6A8):c.*18C>G rs782159926 0.00001
NM_005629.4(SLC6A8):c.1431G>A (p.Ser477=) rs1060453 0.00001
NM_005629.4(SLC6A8):c.1719G>A (p.Pro573=) rs2314070 0.00001
NM_005629.4(SLC6A8):c.204C>T (p.Phe68=) rs782128137 0.00001
NM_005629.4(SLC6A8):c.102C>T (p.Gly34=)
NM_005629.4(SLC6A8):c.1050G>C (p.Gly350=) rs1403430635
NM_005629.4(SLC6A8):c.114G>A (p.Val38=) rs2148358489
NM_005629.4(SLC6A8):c.1245C>G (p.Leu415=) rs782030501
NM_005629.4(SLC6A8):c.1255-44del
NM_005629.4(SLC6A8):c.1393-7C>T rs373525249
NM_005629.4(SLC6A8):c.1518C>T (p.Asp506=) rs1603217612
NM_005629.4(SLC6A8):c.1692C>G (p.Phe564Leu) rs201044530
NM_005629.4(SLC6A8):c.1692C>T (p.Phe564=) rs201044530
NM_005629.4(SLC6A8):c.174G>A (p.Gln58=) rs1557043848
NM_005629.4(SLC6A8):c.1767+11dup rs1557045747
NM_005629.4(SLC6A8):c.1899T>C (p.Ser633=) rs2091483278
NM_005629.4(SLC6A8):c.453G>A (p.Val151=) rs1603215003
NM_005629.4(SLC6A8):c.52AAG[1] (p.Lys19del) rs1603212916
NM_005629.4(SLC6A8):c.681G>A (p.Val227=) rs370508642
NM_005629.4(SLC6A8):c.778-8C>G rs781860529
NM_005629.4(SLC6A8):c.87G>A (p.Gly29=) rs782373793

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