ClinVar Miner

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

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_005629.4(SLC6A8):c.1437C>T (p.Ser479=) rs140115896 0.00334
NM_005629.4(SLC6A8):c.777+4C>T rs201581661 0.00063
NM_005629.4(SLC6A8):c.1597-19G>A rs202118923 0.00057
NM_005629.4(SLC6A8):c.1016+9C>T rs190690083 0.00047
NM_005629.4(SLC6A8):c.1649C>G (p.Thr550Ser) rs199635059 0.00033
NM_005629.4(SLC6A8):c.1767+15C>T rs370331295 0.00029
NM_005629.4(SLC6A8):c.1678A>G (p.Met560Val) rs145438966 0.00024
NM_005629.4(SLC6A8):c.1890G>C (p.Val630=) rs376385129 0.00023
NM_005629.4(SLC6A8):c.807C>T (p.Tyr269=) rs141219551 0.00023
NM_005629.4(SLC6A8):c.645-14C>T rs782227426 0.00021
NM_005629.4(SLC6A8):c.1016+10G>A rs371905179 0.00017
NM_005629.4(SLC6A8):c.-11C>T rs781794844 0.00014
NM_005629.4(SLC6A8):c.1016+12C>T rs182984520 0.00014
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.1496-4G>A rs782589547 0.00010
NM_005629.4(SLC6A8):c.912+9G>A rs782694291 0.00010
NM_005629.4(SLC6A8):c.282C>T (p.Tyr94=) rs375818489 0.00009
NM_005629.4(SLC6A8):c.856C>T (p.Leu286=) rs782005985 0.00009
NM_005629.4(SLC6A8):c.1597-20C>T rs781894858 0.00007
NM_005629.4(SLC6A8):c.1038C>T (p.Leu346=) rs369716393 0.00006
NM_005629.4(SLC6A8):c.1496-17G>A rs375265267 0.00006
NM_005629.4(SLC6A8):c.498G>A (p.Thr166=) rs201260657 0.00005
NM_005629.4(SLC6A8):c.1885G>A (p.Val629Ile) rs781899045 0.00004
NM_005629.4(SLC6A8):c.1161C>T (p.Ile387=) rs782582952 0.00003
NM_005629.4(SLC6A8):c.1601T>C (p.Ile534Thr) rs797045971 0.00003
NM_005629.4(SLC6A8):c.1414C>T (p.Leu472=) rs781974297 0.00002
NM_005629.4(SLC6A8):c.144C>T (p.Ala48=) rs782232933 0.00002
NM_005629.4(SLC6A8):c.639C>T (p.Phe213=) rs1057523082 0.00002
NM_005629.4(SLC6A8):c.644+8C>T rs782433720 0.00002
NM_005629.4(SLC6A8):c.1053C>G (p.Thr351=) rs1557045138 0.00001
NM_005629.4(SLC6A8):c.1290C>T (p.Leu430=) rs782667574 0.00001
NM_005629.4(SLC6A8):c.1404C>T (p.Tyr468=) rs782696303 0.00001
NM_005629.4(SLC6A8):c.1768-10T>C rs1459295373 0.00001
NM_005629.4(SLC6A8):c.1768-16T>C rs370937021 0.00001
NM_005629.4(SLC6A8):c.395-9C>T rs782540675 0.00001
NM_005629.4(SLC6A8):c.405C>T (p.Tyr135=) rs782249346 0.00001
NM_005629.4(SLC6A8):c.459C>T (p.Ala153=) rs782593568 0.00001
NM_005629.4(SLC6A8):c.557G>A (p.Arg186His) rs372601430 0.00001
NM_005629.4(SLC6A8):c.627T>C (p.Pro209=) rs1057521539 0.00001
NM_005629.4(SLC6A8):c.644+20G>A rs782635587 0.00001
NM_005629.4(SLC6A8):c.913-13G>T rs1176497805 0.00001
NM_005629.4(SLC6A8):c.951C>T (p.Tyr317=) rs371516458 0.00001
NM_005629.4(SLC6A8):c.*3_*7del rs1064794768
NM_005629.4(SLC6A8):c.-5del rs1557043702
NM_005629.4(SLC6A8):c.1323C>T (p.Phe441=) rs1057523404
NM_005629.4(SLC6A8):c.1392+17dup rs781964988
NM_005629.4(SLC6A8):c.1393-7C>T rs373525249
NM_005629.4(SLC6A8):c.1416G>A (p.Leu472=) rs1557045478
NM_005629.4(SLC6A8):c.1495+8A>G rs1057523669
NM_005629.4(SLC6A8):c.1632G>C (p.Pro544=) rs782393373
NM_005629.4(SLC6A8):c.1677C>T (p.Ala559=) rs1057522460
NM_005629.4(SLC6A8):c.1767+11C>A rs782709232
NM_005629.4(SLC6A8):c.1767+11C>T rs782709232
NM_005629.4(SLC6A8):c.1767+20C>T rs782612504
NM_005629.4(SLC6A8):c.1767+5G>A rs1557045744
NM_005629.4(SLC6A8):c.1767+8_1767+11dup rs1185206859
NM_005629.4(SLC6A8):c.267G>A (p.Val89=) rs1557044166
NM_005629.4(SLC6A8):c.30C>T (p.Ile10=) rs1057522627
NM_005629.4(SLC6A8):c.354C>T (p.Ala118=) rs1557044183
NM_005629.4(SLC6A8):c.471T>C (p.Tyr157=) rs1057521561
NM_005629.4(SLC6A8):c.87G>A (p.Gly29=) rs782373793
NM_005629.4(SLC6A8):c.912+19G>A rs782518872
NM_005629.4(SLC6A8):c.913-17C>G rs1057524229
NM_005629.4(SLC6A8):c.990C>T (p.Tyr330=) rs1057523301

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