ClinVar Miner

List of variants in gene SLC6A8 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_005629.4(SLC6A8):c.813C>T (p.Val271=) rs138064933 0.00248
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.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.807C>T (p.Tyr269=) rs141219551 0.00023
NM_005629.4(SLC6A8):c.645-6C>T rs377181706 0.00016
NM_005629.4(SLC6A8):c.1533C>T (p.Ile511=) rs782114947 0.00011
NM_005629.4(SLC6A8):c.87G>C (p.Gly29=) rs782373793 0.00011
NM_005629.4(SLC6A8):c.1452C>G (p.Leu484=) rs376421364 0.00009
NM_005629.4(SLC6A8):c.856C>T (p.Leu286=) rs782005985 0.00009
NM_005629.4(SLC6A8):c.1038C>T (p.Leu346=) rs369716393 0.00006
NM_005629.4(SLC6A8):c.1713C>T (p.Cys571=) rs782244505 0.00005
NM_005629.4(SLC6A8):c.498G>A (p.Thr166=) rs201260657 0.00005
NM_005629.4(SLC6A8):c.1632G>A (p.Pro544=) rs782393373 0.00004
NM_005629.4(SLC6A8):c.283G>A (p.Val95Ile) rs782040427 0.00004
NM_005629.4(SLC6A8):c.1285C>G (p.Leu429Val) rs782551106 0.00003
NM_005629.4(SLC6A8):c.1869C>T (p.Ser623=) rs782748657 0.00003
NM_005629.4(SLC6A8):c.1683C>A (p.Gly561=) rs1286428662 0.00002
NM_005629.4(SLC6A8):c.1071C>T (p.Phe357=) rs782782179 0.00001
NM_005629.4(SLC6A8):c.1290C>T (p.Leu430=) rs782667574 0.00001
NM_005629.4(SLC6A8):c.708C>T (p.Thr236=) rs782489930 0.00001
NM_005629.4(SLC6A8):c.786C>T (p.Tyr262=) rs1557044940 0.00001
NM_005629.4(SLC6A8):c.823C>T (p.Leu275=) rs1557044951 0.00001
NM_005629.4(SLC6A8):c.113T>C (p.Val38Ala)
NM_005629.4(SLC6A8):c.124A>G (p.Thr42Ala)
NM_005629.4(SLC6A8):c.153G>A (p.Pro51=) rs782351119
NM_005629.4(SLC6A8):c.1720C>T (p.Leu574=) rs1569539472
NM_005629.4(SLC6A8):c.1861C>T (p.Pro621Ser) rs782388832
NM_005629.4(SLC6A8):c.1887C>T (p.Val629=) rs1485660118
NM_005629.4(SLC6A8):c.318C>T (p.Phe106=) rs1569539245
NM_005629.4(SLC6A8):c.354C>G (p.Ala118=) rs1557044183
NM_005629.4(SLC6A8):c.672A>G (p.Gly224=) rs1569539299
NM_005629.4(SLC6A8):c.981G>A (p.Leu327=) rs1569539360

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