| | | 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 | |
| | RANBP2, SH3RF3 +1 more (I140V) | 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 | |
| | RANBP2, SH3RF3 +1 more (R34Q) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | RANBP2, SH3RF3 +1 more (C87S) | 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 | |
| | RANBP2, SEPTIN10 (Y135C +6 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | RANBP2, SEPTIN10 (P166L +6 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | RANBP2, SEPTIN10 (R315L +9 more) | Single nucleotide variant (missense 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CCDC138, RANBP2 (R150W +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | CCDC138, RANBP2 (T139A +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | CCDC138, RANBP2 (Q150H +7 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | CCDC138, RANBP2 (I371V +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CCDC138, RANBP2 (D321G +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CCDC138, LOC129934529 +1 more (A22P +1 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | CCDC138, RANBP2 (L131F +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | CCDC138, RANBP2 (K250E +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | CCDC138, RANBP2 (D52E +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion | Familial acute necrotizing encephalopathy | |
| | | Single nucleotide variant (missense variant) | Familial acute necrotizing encephalopathy | |
| | | 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 | |
| | RANBP2, SH3RF3 +1 more (R33H) | 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 | |
| | RANBP2, SH3RF3 +1 more (A182S) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | RANBP2, SH3RF3 +1 more (R179W) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | RANBP2, SH3RF3 +1 more (S168F) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | RANBP2, SH3RF3 +1 more (S130I) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | RANBP2, SH3RF3 +1 more (H90Q) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | RANBP2, SH3RF3 +1 more (F77L) | 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 | |
| | RANBP2, SH3RF3 +1 more (A37V) | 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 | |
| | RANBP2, SEPTIN10 (R144L +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (N297Y +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (L112P +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (R166Q +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (Q256E +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (R255H +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (R255C +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (V243G +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (M107I +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (G104R +9 more) | Single nucleotide variant (missense variant) | not specified | |
| | RANBP2, SEPTIN10 (V220A +9 more) | Single nucleotide variant (missense variant) | not specified | |