| | FBXO11, MSH6 (L817F +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | FBXO11, MSH6 (T839R +1 more) | Single nucleotide variant (missense variant +1 more) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | FBXO11-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, MSH6 (I819del +1 more) | Microsatellite (inframe_deletion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (Q29P) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Insertion (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (P33Q) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (Q42P) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (Q34P) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FBXO11, LOC100506235 (P31Q) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (P41L) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FBXO11, LOC100506235 (A6T) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Duplication (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Microsatellite (non-coding transcript variant +1 more) | not provided | |
| | | Microsatellite (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (N2S) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (A7G) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, MSH6 (P814S +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (P11S) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | FBXO11, MSH6 (T771S +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (P47L) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (R9G) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FBXO11, MSH6 (I826T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Duplication (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FBXO11, LOC100506235 (V14A) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | FBXO11, MSH6 (N794S +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FBXO11, LOC100506235 (Q37L) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (P11L) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | FBXO11, LOC100506235 (P33S) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FBXO11, LOC100506235 (A7V) | Single nucleotide variant (non-coding transcript variant +1 more) | FBXO11-related disorder | |
| | FBXO11, MSH6 (I780L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | FBXO11, MSH6 (D826Y +1 more) | Single nucleotide variant (missense variant +1 more) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | FBXO11, MSH6 (A705T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FBXO11, MSH6 (I742V +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | FBXO11, MSH6 (H764Y +1 more) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | FBXO11, MSH6 (A832V +1 more) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | |
| | | Single nucleotide variant (missense variant) | Developmental disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | FBXO11, LOC100506235 (Q29R) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FBXO11, MSH6 (H907fs +1 more) | Deletion (frameshift variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities +1 more | |
| | | Duplication (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |