List of variants in gene SLC2A1 reported as likely benign by Ambry Genetics

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.1296C>T (p.Tyr432=)	rs75485205	0.00267
NM_006516.4(SLC2A1):c.27G>A (p.Thr9=)	rs34025424	0.00176
NM_006516.4(SLC2A1):c.507C>T (p.Leu169=)	rs115541691	0.00102
NM_006516.4(SLC2A1):c.894C>T (p.Phe298=)	rs140825318	0.00073
NM_006516.4(SLC2A1):c.777C>T (p.Ile259=)	rs78388808	0.00068
NM_006516.4(SLC2A1):c.1437C>T (p.Pro479=)	rs146879902	0.00065
NM_006516.4(SLC2A1):c.498C>T (p.Val166=)	rs150971143	0.00036
NM_006516.4(SLC2A1):c.895G>A (p.Glu299Lys)	rs148518827	0.00031
NM_006516.4(SLC2A1):c.972+17T>A	rs202140308	0.00017
NM_006516.4(SLC2A1):c.764A>C (p.Lys255Thr)	rs5811	0.00013
NM_006516.4(SLC2A1):c.312C>G (p.Phe104Leu)	rs76672402	0.00010
NM_006516.4(SLC2A1):c.1395C>T (p.Ser465=)	rs75852730	0.00008
NM_006516.4(SLC2A1):c.543C>T (p.Gly181=)	rs377674001	0.00008
NM_006516.4(SLC2A1):c.987G>A (p.Glu329=)	rs201989024	0.00008
NM_006516.4(SLC2A1):c.1005C>G (p.Thr335=)	rs763664146	0.00006
NM_006516.4(SLC2A1):c.188C>T (p.Thr63Met)	rs200828053	0.00006
NM_006516.4(SLC2A1):c.1034C>T (p.Ala345Val)	rs769943554	0.00004
NM_006516.4(SLC2A1):c.180G>A (p.Thr60=)	rs780638574	0.00004
NM_006516.4(SLC2A1):c.606C>T (p.Ile202=)	rs779779804	0.00004
NM_006516.4(SLC2A1):c.657C>T (p.Asn219=)	rs534113895	0.00004
NM_006516.4(SLC2A1):c.339G>A (p.Ser113=)	rs755571737	0.00003
NM_006516.4(SLC2A1):c.624C>G (p.Pro208=)	rs778522408	0.00003
NM_006516.4(SLC2A1):c.495C>T (p.Val165=)	rs181115612	0.00002
NM_006516.4(SLC2A1):c.708C>T (p.Asp236=)	rs566497194	0.00002
NM_006516.4(SLC2A1):c.804C>T (p.Tyr268=)	rs1370873840	0.00002
NM_006516.4(SLC2A1):c.1134C>T (p.Phe378=)	rs758184335	0.00001
NM_006516.4(SLC2A1):c.123G>A (p.Glu41=)	rs769414573	0.00001
NM_006516.4(SLC2A1):c.1297G>A (p.Val433Ile)	rs200819771	0.00001
NM_006516.4(SLC2A1):c.189G>A (p.Thr63=)	rs766043826	0.00001
NM_006516.4(SLC2A1):c.318C>T (p.Ser106=)	rs760599149	0.00001
NM_006516.4(SLC2A1):c.746G>A (p.Arg249Gln)	rs587784395	0.00001
NM_006516.4(SLC2A1):c.1023C>T (p.Leu341=)	rs143588685
NM_006516.4(SLC2A1):c.1155C>T (p.Pro385=)	rs76860965
NM_006516.4(SLC2A1):c.183C>A (p.Leu61=)
NM_006516.4(SLC2A1):c.312C>T (p.Phe104=)	rs76672402
NM_006516.4(SLC2A1):c.387C>G (p.Ile129Met)	rs751907207

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