ClinVar Miner

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

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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NM_004371.4(COPA):c.1491A>G (p.Ser497=) rs1047288998
NM_004371.4(COPA):c.1667+9A>G rs375429812
NM_004371.4(COPA):c.2015A>T (p.Asn672Ile) rs147312908
NM_004371.4(COPA):c.2420A>C (p.Asn807Thr) rs199630217
NM_004371.4(COPA):c.2483G>A (p.Gly828Glu) rs144241395
NM_004371.4(COPA):c.2531G>A (p.Gly844Asp) rs143115096
NM_004371.4(COPA):c.2683T>G (p.Ser895Ala) rs139398871
NM_004371.4(COPA):c.2808C>T (p.Phe936=) rs760354732
NM_004371.4(COPA):c.3423C>T (p.Thr1141=) rs776753399
NM_004371.4(COPA):c.3433C>T (p.Leu1145=) rs747075563
NM_004371.4(COPA):c.3483C>T (p.Asp1161=) rs376400505
NM_004371.4(COPA):c.607-5T>C rs1167456164
NM_004371.4(COPA):c.607-8_607-7del rs1553206195
NM_004371.4(COPA):c.657T>G (p.Leu219=) rs1571174206
NM_004371.4(COPA):c.753T>C (p.Asn251=) rs374078706

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