ClinVar Miner

List of variants in gene COPA reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_004371.3(COPA):c.1005T>C (p.Tyr335=) rs74125578
NM_004371.3(COPA):c.1741C>T (p.Leu581=) rs79304843
NM_004371.3(COPA):c.192A>G (p.Pro64=) rs143827776
NM_004371.3(COPA):c.2263+7A>G rs116596416
NM_004371.3(COPA):c.2319C>T (p.Ser773=) rs74125574
NM_004371.3(COPA):c.2754+4A>G rs75190422
NM_004371.3(COPA):c.297G>A (p.Thr99=) rs77097084
NM_004371.3(COPA):c.399G>A (p.Gly133=) rs142221638
NM_004371.3(COPA):c.436A>G (p.Thr146Ala) rs57425682
NM_004371.3(COPA):c.994A>G (p.Met332Val) rs115066135

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