| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861892, PRMT5 (A159V +4 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PRMT5, PRMT5-AS1 (M358V +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | LOC126861892, PRMT5 (S214P +4 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PRMT5, PRMT5-AS1 (A381S +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRMT5, PRMT5-AS1 (S564F +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC126861892, PRMT5 (R203H +4 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PRMT5, PRMT5-AS1 (R431H +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | PRMT5, PRMT5-AS1 (K504Q +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC126861892, PRMT5 (E116Q +4 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
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