ClinVar Miner

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

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_000341.3(SLC3A1):c.-65C>T rs886056066
NM_000341.4(SLC3A1):c.1012G>C (p.Asp338His) rs140452488
NM_000341.4(SLC3A1):c.1074C>T (p.His358=) rs754041697
NM_000341.4(SLC3A1):c.1137-3T>C rs555017366
NM_000341.4(SLC3A1):c.1200A>G (p.Pro400=) rs886056069
NM_000341.4(SLC3A1):c.1258T>G (p.Ser420Ala) rs370023281
NM_000341.4(SLC3A1):c.1269C>T (p.Ser423=) rs557669708
NM_000341.4(SLC3A1):c.1334T>C (p.Ile445Thr) rs187962930
NM_000341.4(SLC3A1):c.1400T>A (p.Met467Lys) rs121912691
NM_000341.4(SLC3A1):c.1495G>T (p.Asp499Tyr) rs886056070
NM_000341.4(SLC3A1):c.1510C>T (p.Arg504Cys) rs201143887
NM_000341.4(SLC3A1):c.166G>A (p.Glu56Lys) rs886056067
NM_000341.4(SLC3A1):c.184G>A (p.Val62Ile) rs778587102
NM_000341.4(SLC3A1):c.24A>C (p.Arg8Ser) rs376615998
NM_000341.4(SLC3A1):c.303C>T (p.Ile101=) rs752281627
NM_000341.4(SLC3A1):c.395A>G (p.Lys132Arg) rs148787131
NM_000341.4(SLC3A1):c.417C>T (p.Asn139=) rs150870922
NM_000341.4(SLC3A1):c.460G>T (p.Ala154Ser) rs766140035
NM_000341.4(SLC3A1):c.478G>C (p.Val160Leu) rs886056068
NM_000341.4(SLC3A1):c.572A>G (p.Glu191Gly) rs534054965
NM_000341.4(SLC3A1):c.685C>T (p.Arg229Trp) rs758636942
NM_000341.4(SLC3A1):c.788G>C (p.Ser263Thr) rs139310305
NM_000341.4(SLC3A1):c.892-6C>G rs114640930

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