ClinVar Miner

List of variants in gene SLC13A3 reported as benign for not provided

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_022829.6(SLC13A3):c.1278C>T (p.Pro426=) rs1880898 0.58688
NM_022829.6(SLC13A3):c.207C>G (p.Leu69=) rs2273024 0.30359
NM_022829.6(SLC13A3):c.908G>C (p.Gly303Ala) rs141554970 0.01782
NM_022829.6(SLC13A3):c.1035T>A (p.Val345=) rs35393013 0.01294
NM_022829.6(SLC13A3):c.1121+18C>T rs188079387 0.00370
NM_022829.6(SLC13A3):c.813C>T (p.Asp271=) rs139209119 0.00137
NM_022829.6(SLC13A3):c.412T>C (p.Leu138=) rs141910662 0.00124
NM_022829.6(SLC13A3):c.1632+13del rs140718691 0.00115
NM_022829.6(SLC13A3):c.1518C>G (p.Pro506=) rs139887313 0.00097
NM_022829.6(SLC13A3):c.957T>C (p.Asn319=) rs191161551 0.00026
NM_022829.6(SLC13A3):c.292A>T (p.Ile98Phe) rs201443231 0.00013
NM_022829.6(SLC13A3):c.903C>T (p.Tyr301=) rs146172910 0.00012
NM_022829.6(SLC13A3):c.118C>T (p.Arg40Cys) rs77731467
NM_022829.6(SLC13A3):c.1333-4G>T rs8116973
NM_022829.6(SLC13A3):c.1392C>T (p.Pro464=)
NM_022829.6(SLC13A3):c.1458G>C (p.Ala486=) rs202391
NM_022829.6(SLC13A3):c.336C>T (p.Ile112=) rs200268336
NM_022829.6(SLC13A3):c.891C>T (p.Ile297=)

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