ClinVar Miner

List of variants in gene C16orf58, SLC5A2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_003041.3(SLC5A2):c.*63G>A rs114517938
NM_003041.3(SLC5A2):c.1692G>A (p.Arg564=) rs147697689
NM_003041.3(SLC5A2):c.1719G>T (p.Leu573=) rs767926604
NM_003041.3(SLC5A2):c.1773G>T (p.Glu591Asp) rs149525864
NM_003041.3(SLC5A2):c.1792+12T>C rs886051963
NM_003041.3(SLC5A2):c.1844G>C (p.Cys615Ser) rs201073991
NM_003041.3(SLC5A2):c.1877C>T (p.Pro626Leu) rs535031004
NM_003041.3(SLC5A2):c.1885A>G (p.Thr629Ala) rs61741237
NM_003041.3(SLC5A2):c.1895A>C (p.Glu632Ala) rs753477563
NM_003041.3(SLC5A2):c.1895_1897delAGG (p.Glu632del) rs771257793
NM_003041.3(SLC5A2):c.1902G>A (p.Ala634=) rs372404252
NM_003041.3(SLC5A2):c.1926C>T (p.Asp642=) rs557690622
NM_003041.3(SLC5A2):c.1933G>A (p.Glu645Lys) rs760556743
NM_003041.3(SLC5A2):c.1961A>G (p.Asn654Ser) rs61742739
NM_003041.3(SLC5A2):c.1982T>C (p.Met661Thr) rs775638719

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