| | | 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 | |
| | TMEM132D, TMEM132D-AS2 (T444M) | Single nucleotide variant (non-coding transcript variant +1 more) | 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) | TMEM132D-related disorder | |
| | | Single nucleotide variant (missense variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (missense variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (missense variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (intron variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (missense variant) | TMEM132D-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMEM132D-related disorder | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | TMEM132D-related disorder +1 more | |
| | | 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 | |
| | TMEM132D, TMEM132D-AS2 (V479M) | 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 | |
| | TMEM132D, TMEM132D-AS2 (L467P) | Single nucleotide variant (non-coding transcript variant +1 more) | 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 | |
| | TMEM132D, TMEM132D-AS2 (G461S) | Single nucleotide variant (non-coding transcript variant +1 more) | 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 (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 (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 (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 | |