ClinVar Miner

Variants in gene CCDC88C with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 9
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HGVS dbSNP
NM_001080414.4(CCDC88C):c.1962G>A (p.Leu654=) rs61746076
NM_001080414.4(CCDC88C):c.3900C>T (p.Phe1300=) rs199536020
NM_001080414.4(CCDC88C):c.4433T>C (p.Val1478Ala) rs201222692
NM_001080414.4(CCDC88C):c.4668G>A (p.Leu1556=) rs139544500
NM_001080414.4(CCDC88C):c.4707G>A (p.Arg1569=) rs145210051
NM_001080414.4(CCDC88C):c.4889G>A (p.Arg1630His) rs115510695
NM_001080414.4(CCDC88C):c.5951G>A (p.Arg1984Gln) rs61745465
NM_001080414.4(CCDC88C):c.766C>T (p.Leu256=) rs183742506
NM_001080414.4(CCDC88C):c.912C>T (p.Asp304=) rs61736349

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