| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | PHC2, PHC2-AS1 (R486W +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | PHC2, PHC2-AS1 (T267M +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (A144T +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (T484M +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (G197A +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (P400L +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (P275S +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (Q428K +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (A276S +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | PHC2, PHC2-AS1 (A467D +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | PHC2, PHC2-AS1 (P514L +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | PHC2, PHC2-AS1 (R367Q +4 more) | Single nucleotide variant (missense variant) | not provided | |
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