ClinVar Miner

List of variants in gene CA2 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_000067.3(CA2):c.*17G>A rs140653628
NM_000067.3(CA2):c.*303C>T rs150089617
NM_000067.3(CA2):c.*374A>G rs886063151
NM_000067.3(CA2):c.*465A>C rs886063152
NM_000067.3(CA2):c.*562T>C rs886063153
NM_000067.3(CA2):c.139_142CTGT[1] (p.Ser48fs) rs1564077060
NM_000067.3(CA2):c.40G>A (p.Glu14Lys) rs758659684
NM_000067.3(CA2):c.508-7G>A rs886063149
NM_000067.3(CA2):c.539C>T (p.Pro180Leu) rs886063150
NM_000067.3(CA2):c.648C>T (p.Ser216=) rs376387073

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