| | | 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 (synonymous variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFP36L2-related disorder | |
| | LOC129933607, ZFP36L2 (A329V) | Single nucleotide variant (missense variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (missense variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (missense variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (missense variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFP36L2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | 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 | |
| | LOC129933607, ZFP36L2 (G402V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A330V) | 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 | |
| | LOC129933607, ZFP36L2 (R393C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A387V) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A356V) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A329T) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A348D) | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | LOC129933607, ZFP36L2 (Q396H) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A351S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A364V) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933607, ZFP36L2 (A377P) | 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 | |
| | LOC129933607, ZFP36L2 (A364T) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Oocyte maturation defect 13 | |
| | | Deletion (inframe_deletion) | Oocyte maturation defect 13 | |
| | | Copy number loss | See cases | |
| | | Copy number gain | Mosaic trisomy 2 | |
| | | Copy number gain | See cases | |
| | | Copy number gain | not provided | |
| | ZFP36L2, LOC129933606 (S476fs) | Duplication (frameshift variant) | not provided | |
| | | Copy number gain | not provided | |
| | | Deletion | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Inversion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126806252, LOC126806253 +2457 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |