| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (V768I +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (S859T +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (R858H +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (T842M +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (T688M +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (A862E +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (L810F +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (L839V +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (I655M +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (S831R +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (N617H +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (F602L +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (intron variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | ATP2C2, ATP2C2-AS1 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | ATP2C2, ATP2C2-AS1 (T788A) | Single nucleotide variant (non-coding transcript variant +2 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (intron variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | ATP2C2, ATP2C2-AS1 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | ATP2C2, ATP2C2-AS1 (P624Q +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (missense variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (intron variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (intron variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ATP2C2-related disorder | |
| | ATP2C2, ATP2C2-AS1 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | ATP2C2, ATP2C2-AS1 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | ATP2C2, ATP2C2-AS1 (G629W +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | ATP2C2-related disorder +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | ATP2C2, ATP2C2-AS1 (S742C +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ATP2C2, ATP2C2-AS1 (A842P +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (D636E +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (M723I +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (I739F +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ATP2C2, ATP2C2-AS1 (A592T +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ATP2C2, ATP2C2-AS1 +1 more (S859C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (G629R +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ATP2C2, ATP2C2-AS1 (L915S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |