ClinVar Miner

List of variants in gene SLC35A1 studied for abdominal and pelvic region disorder

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_006416.4(SLC35A1):c.[147T>C;277delG;281delC]
NM_006416.5(SLC35A1):c.1000G>A (p.Val334Ile)
NM_006416.5(SLC35A1):c.133A>G (p.Thr45Ala) rs145006535
NM_006416.5(SLC35A1):c.19A>C (p.Asn7His) rs114156788
NM_006416.5(SLC35A1):c.303G>C (p.Gln101His) rs1554166294
NM_006416.5(SLC35A1):c.355-7T>C rs774147829
NM_006416.5(SLC35A1):c.400T>C (p.Leu134=) rs866423704
NM_006416.5(SLC35A1):c.467C>G (p.Thr156Arg) rs578205635
NM_006416.5(SLC35A1):c.507+8A>G rs201797109
NM_006416.5(SLC35A1):c.556T>C (p.Leu186=) rs147999550
NM_006416.5(SLC35A1):c.558G>A (p.Leu186=) rs368921086
NM_006416.5(SLC35A1):c.569T>C (p.Phe190Ser) rs763621828
NM_006416.5(SLC35A1):c.586G>A (p.Glu196Lys) rs1554166844
NM_006416.5(SLC35A1):c.699T>G (p.Ile233Met) rs150233994
NM_006416.5(SLC35A1):c.757G>C (p.Ala253Pro) rs1484245900

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