List of variants in gene SLC22A6 reported as uncertain significance for not specified

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: 52

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HGVS	dbSNP	gnomAD frequency
NM_153276.3(SLC22A6):c.700C>G (p.Gln234Glu)	rs751215054	0.00008
NM_153276.3(SLC22A6):c.664G>A (p.Val222Met)	rs1416600616	0.00004
NM_153276.3(SLC22A6):c.239G>A (p.Arg80His)	rs755249293	0.00003
NM_153276.3(SLC22A6):c.319G>A (p.Asp107Asn)	rs565805838	0.00003
NM_153276.3(SLC22A6):c.1360C>T (p.Arg454Trp)	rs1289616706	0.00001
NM_153276.3(SLC22A6):c.1392G>T (p.Met464Ile)	rs756411177	0.00001
NM_153276.3(SLC22A6):c.1431G>A (p.Met477Ile)	rs1239443098	0.00001
NM_153276.3(SLC22A6):c.1438G>A (p.Glu480Lys)	rs1230203789	0.00001
NM_153276.3(SLC22A6):c.164C>T (p.Ala55Val)	rs202055464	0.00001
NM_153276.3(SLC22A6):c.185G>C (p.Gly62Ala)	rs144803446	0.00001
NM_153276.3(SLC22A6):c.44G>A (p.Arg15His)	rs751931872	0.00001
NM_153276.3(SLC22A6):c.785T>C (p.Phe262Ser)	rs1266103870	0.00001
NM_153276.3(SLC22A6):c.1009C>T (p.His337Tyr)
NM_153276.3(SLC22A6):c.1016T>G (p.Phe339Cys)
NM_153276.3(SLC22A6):c.1069G>C (p.Val357Leu)
NM_153276.3(SLC22A6):c.1082A>C (p.Gln361Pro)
NM_153276.3(SLC22A6):c.1099A>C (p.Ile367Leu)	rs770039912
NM_153276.3(SLC22A6):c.1130T>C (p.Val377Ala)
NM_153276.3(SLC22A6):c.1147C>T (p.Leu383Phe)	rs2539600418
NM_153276.3(SLC22A6):c.1183C>T (p.Arg395Trp)
NM_153276.3(SLC22A6):c.1184G>C (p.Arg395Pro)
NM_153276.3(SLC22A6):c.1247C>A (p.Pro416His)
NM_153276.3(SLC22A6):c.1315A>T (p.Asn439Tyr)
NM_153276.3(SLC22A6):c.1408A>G (p.Ile470Val)
NM_153276.3(SLC22A6):c.1411G>A (p.Val471Met)
NM_153276.3(SLC22A6):c.1428C>A (p.Ser476Arg)	rs1181669528
NM_153276.3(SLC22A6):c.1454T>C (p.Met485Thr)	rs2539595452
NM_153276.3(SLC22A6):c.1456C>A (p.Pro486Thr)	rs760201276
NM_153276.3(SLC22A6):c.1493G>C (p.Ser498Thr)
NM_153276.3(SLC22A6):c.1495G>T (p.Ala499Ser)
NM_153276.3(SLC22A6):c.1552G>A (p.Asp518Asn)
NM_153276.3(SLC22A6):c.1628C>T (p.Ser543Leu)
NM_153276.3(SLC22A6):c.206G>A (p.Arg69Gln)
NM_153276.3(SLC22A6):c.251C>T (p.Pro84Leu)
NM_153276.3(SLC22A6):c.254A>C (p.Gln85Pro)
NM_153276.3(SLC22A6):c.375C>A (p.Asp125Glu)
NM_153276.3(SLC22A6):c.449T>C (p.Met150Thr)	rs2539609558
NM_153276.3(SLC22A6):c.485G>A (p.Arg162Gln)
NM_153276.3(SLC22A6):c.4G>T (p.Ala2Ser)
NM_153276.3(SLC22A6):c.569C>T (p.Ala190Val)	rs2539608230
NM_153276.3(SLC22A6):c.584C>T (p.Ser195Leu)
NM_153276.3(SLC22A6):c.620T>A (p.Met207Lys)	rs2539607984
NM_153276.3(SLC22A6):c.640A>T (p.Met214Leu)	rs2086261483
NM_153276.3(SLC22A6):c.665T>G (p.Val222Gly)
NM_153276.3(SLC22A6):c.719T>G (p.Val240Gly)
NM_153276.3(SLC22A6):c.725A>T (p.Tyr242Phe)
NM_153276.3(SLC22A6):c.727G>T (p.Ala243Ser)
NM_153276.3(SLC22A6):c.802T>C (p.Phe268Leu)
NM_153276.3(SLC22A6):c.858G>T (p.Arg286Ser)	rs141733197
NM_153276.3(SLC22A6):c.878G>A (p.Arg293Gln)
NM_153276.3(SLC22A6):c.892C>T (p.Arg298Trp)
NM_153276.3(SLC22A6):c.958G>A (p.Gly320Ser)

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