ClinVar Miner

List of variants in gene combination PREPL, SLC3A1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000341.4(SLC3A1):c.*100T>C rs886056074
NM_000341.4(SLC3A1):c.1626G>T (p.Lys542Asn) rs886056071
NM_000341.4(SLC3A1):c.1717T>C (p.Leu573=) rs148703534
NM_000341.4(SLC3A1):c.1742T>G (p.Val581Gly) rs886056072
NM_000341.4(SLC3A1):c.1767C>T (p.Ile589=) rs142141929
NM_000341.4(SLC3A1):c.1810C>T (p.Leu604=) rs770801300
NM_000341.4(SLC3A1):c.1854_1859del (p.Met618_Arg619del) rs886056073
NM_000341.4(SLC3A1):c.1973G>A (p.Arg658His) rs370262167

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