List of variants in gene SLC6A8 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
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.1890G>C (p.Val630=)	rs376385129	0.00023
NM_005629.4(SLC6A8):c.1473C>T (p.Cys491=)	rs122453118	0.00013
NM_005629.4(SLC6A8):c.87G>C (p.Gly29=)	rs782373793	0.00011
NM_005629.4(SLC6A8):c.1570T>A (p.Ser524Thr)	rs782703394	0.00010
NM_005629.4(SLC6A8):c.1452C>G (p.Leu484=)	rs376421364	0.00009
NM_005629.4(SLC6A8):c.1497A>G (p.Gly499=)	rs199640501	0.00008
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.1646A>C (p.Asn549Thr)	rs782790088	0.00005
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.1614C>T (p.Asn538=)	rs369726574	0.00002
NM_005629.4(SLC6A8):c.537C>T (p.Pro179=)	rs202136567	0.00002
NM_005629.4(SLC6A8):c.1431G>A (p.Ser477=)	rs1060453	0.00001
NM_005629.4(SLC6A8):c.102C>T (p.Gly34=)
NM_005629.4(SLC6A8):c.1255-44del
NM_005629.4(SLC6A8):c.1692C>G (p.Phe564Leu)	rs201044530
NM_005629.4(SLC6A8):c.174G>A (p.Gln58=)	rs1557043848
NM_005629.4(SLC6A8):c.1899T>C (p.Ser633=)	rs2091483278
NM_005629.4(SLC6A8):c.52AAG[1] (p.Lys19del)	rs1603212916
NM_005629.4(SLC6A8):c.778-8C>G	rs781860529

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