| | LOC112577475, RBM15 (P742L) | 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 | |
| | LOC112577475, RBM15 (R636G) | 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 | |
| | LOC129931144, RBM15 (T25A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (P10L) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (S712T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (L695F) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (S691F) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (R35H) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | LOC129931144, RBM15 (V53L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (T733A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (D687G) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Deletion | Hereditary spastic paraplegia 63 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (L614V) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (P21S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (R30Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (S712N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112577475, RBM15 (P606R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (R17W) | 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 | |
| | LOC129931144, RBM15 (L22Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (R11Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931144, RBM15 (T25R) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not specified | |
| | | Deletion | Developmental and epileptic encephalopathy, 32 | |
| | | Copy number loss | Seizure +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion | not provided | |
| | | Deletion | 1p13.3 deletion syndrome | |
| | | Deletion | Autism | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC112577475, RBM15 (Q638K) | Single nucleotide variant (missense variant) | Neuroblastoma | |
| | LOC129388571, LOC129388572 +563 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |