List of variants in gene SLC22A5 reported as likely benign by GeneDx

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_003060.4(SLC22A5):c.952-107C>T	rs73787199	0.01008
NM_003060.4(SLC22A5):c.1268-212G>A	rs113550530	0.00805
NM_003060.4(SLC22A5):c.653-203G>A	rs143232217	0.00772
NM_003060.4(SLC22A5):c.1268-136C>A	rs562878896	0.00568
NM_003060.4(SLC22A5):c.*271T>G	rs116252376	0.00420
NM_003060.4(SLC22A5):c.1267+279G>A	rs80314534	0.00404
NM_003060.4(SLC22A5):c.1451-16G>A	rs140988771	0.00371
NM_003060.4(SLC22A5):c.498-266A>T	rs143429111	0.00365
NM_003060.4(SLC22A5):c.1053-292T>G	rs78200702	0.00351
NM_003060.4(SLC22A5):c.1434C>T (p.Pro478=)	rs140495935	0.00202
NM_003060.4(SLC22A5):c.1052+49T>A	rs144619991	0.00128
NM_003060.4(SLC22A5):c.934A>G (p.Ile312Val)	rs77300588	0.00085
NM_003060.4(SLC22A5):c.1380C>T (p.Asn460=)	rs149521997	0.00079
NM_003060.4(SLC22A5):c.279G>C (p.Ser93=)	rs377734902	0.00073
NM_003060.4(SLC22A5):c.1441G>A (p.Val481Ile)	rs11568513	0.00061
NM_003060.4(SLC22A5):c.1341C>T (p.Tyr447=)	rs58188318	0.00052
NM_003060.4(SLC22A5):c.-26G>A	rs369724970	0.00023
NM_003060.4(SLC22A5):c.798G>A (p.Pro266=)	rs143758508	0.00022
NM_003060.4(SLC22A5):c.1053-3C>T	rs149201271	0.00021
NM_003060.4(SLC22A5):c.1377A>G (p.Arg459=)	rs142264458	0.00018
NM_003060.4(SLC22A5):c.852C>T (p.Leu284=)	rs146185976	0.00017
NM_003060.4(SLC22A5):c.1043T>C (p.Ile348Thr)	rs150544263	0.00016
NM_003060.4(SLC22A5):c.93C>T (p.Pro31=)	rs375293546	0.00009
NM_003060.4(SLC22A5):c.451G>A (p.Val151Met)	rs386134193	0.00003
NM_003060.4(SLC22A5):c.1185A>G (p.Gln395=)	rs916795176	0.00002
NM_003060.4(SLC22A5):c.573G>T (p.Lys191Asn)	rs765204844	0.00002
NM_003060.4(SLC22A5):c.1125C>T (p.Asn375=)	rs202219455	0.00001
NM_003060.4(SLC22A5):c.1267+14G>A	rs769114259	0.00001
NM_003060.4(SLC22A5):c.405G>A (p.Val135=)	rs777083211	0.00001
NM_003060.4(SLC22A5):c.1080G>T (p.Gly360=)	rs139508856
NM_003060.4(SLC22A5):c.1170C>G (p.Ala390=)	rs774368158
NM_003060.4(SLC22A5):c.1451-53A>T	rs77893586
NM_003060.4(SLC22A5):c.394-18C>G	rs200136788

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