ClinVar Miner

List of variants in gene GALE 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: 27
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HGVS dbSNP
NM_001008216.2(GALE):c.*192T>C rs576468712
NM_001008216.2(GALE):c.*326_*328dup rs557214506
NM_001008216.2(GALE):c.*327A>T rs535702110
NM_001008216.2(GALE):c.-77+241C>G rs566996145
NM_001008216.2(GALE):c.-77+340G>C rs568182391
NM_001008216.2(GALE):c.13G>T (p.Val5Leu)
NM_001008216.2(GALE):c.140A>C (p.Glu47Ala) rs367768055
NM_001008216.2(GALE):c.307G>T (p.Asp103Tyr)
NM_001008216.2(GALE):c.330C>T (p.Thr110=) rs377557637
NM_001008216.2(GALE):c.369G>A (p.Gly123=) rs138148991
NM_001008216.2(GALE):c.423C>T (p.Tyr141=) rs138518245
NM_001008216.2(GALE):c.447C>G (p.Pro149=) rs571625657
NM_001008216.2(GALE):c.450G>A (p.Thr150=) rs566884215
NM_001008216.2(GALE):c.488T>G (p.Phe163Cys)
NM_001008216.2(GALE):c.506G>A (p.Arg169Gln) rs140878602
NM_001008216.2(GALE):c.647C>T (p.Ala216Val) rs542192037
NM_001008216.2(GALE):c.648G>A (p.Ala216=) rs144723215
NM_001008216.2(GALE):c.760G>A (p.Ala254Thr)
NM_001008216.2(GALE):c.873+13_873+14insA rs765063773
NM_001008216.2(GALE):c.873+6C>T rs1553130228
NM_001008216.2(GALE):c.873G>A (p.Lys291=)
NM_001008216.2(GALE):c.879G>A (p.Pro293=) rs142332521
NM_001008216.2(GALE):c.912G>A (p.Val304=) rs143694860
NM_001008216.2(GALE):c.923A>G (p.Tyr308Cys) rs780393850
NM_001008216.2(GALE):c.955G>C (p.Gly319Arg) rs752384408
NM_001008216.2(GALE):c.973G>A (p.Gly325Arg)
NM_001008216.2(GALE):c.97G>A (p.Asp33Asn) rs727503945

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