| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129994765, PROB1 (A876G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 (S862C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (R852S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (P822S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (A808T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (G795A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (V791L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (A782V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (G781S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994765, PROB1 +1 more (P778L) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene