ClinVar Miner

List of variants in gene CFI 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: 18
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NM_000204.4(CFI):c.-98T>C rs886058984
NM_000204.4(CFI):c.1112G>T (p.Gly371Val) rs763931500
NM_000204.4(CFI):c.129C>T (p.Cys43=) rs146462954
NM_000204.4(CFI):c.1381T>C (p.Phe461Leu) rs886058983
NM_000204.4(CFI):c.1429+5A>G rs771786368
NM_000204.4(CFI):c.1429G>C (p.Asp477His) rs754972981
NM_000204.4(CFI):c.1516A>C (p.Lys506Gln) rs886058982
NM_000204.4(CFI):c.1532C>T (p.Ala511Val) rs760801046
NM_000204.4(CFI):c.1709G>C (p.Ser570Thr) rs200973120
NM_000204.4(CFI):c.205A>G (p.Lys69Glu) rs771325547
NM_000204.4(CFI):c.209A>C (p.Asn70Thr)
NM_000204.4(CFI):c.309C>T (p.Asn103=) rs761425840
NM_000204.4(CFI):c.405T>C (p.Asp135=) rs375792874
NM_000204.4(CFI):c.540A>G (p.Glu180=) rs759777516
NM_000204.5(CFI):c.1160C>T (p.Thr387Ile)
NM_000204.5(CFI):c.1355C>A (p.Ala452Asp)
NM_000204.5(CFI):c.184A>G (p.Lys62Glu)
NM_000204.5(CFI):c.850T>G (p.Cys284Gly)

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