| | ARMCX5-GPRASP2, GPRASP1 (L1284S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A995V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (M685I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (F584L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (R87Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (M1179V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GPRASP1, ARMCX5-GPRASP2 (T144R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (R463H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A130V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (R110fs) | Microsatellite (frameshift variant +1 more) | not provided | |
| | ARMCX5-GPRASP2, GPRASP1 (Y246C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E208K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (N1385H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (Q1380K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (S1356F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E1343D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (P1252L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (T124I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (P1086S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E1011K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E851K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E7D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (T727I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A726P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (S653N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A648V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (G551D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E539D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (E515K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (S453T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (I434V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A4E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (K353E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (C600W) | Single nucleotide variant (missense variant +1 more) | GPRASP1-related disorder | |
| | GPRASP1, ARMCX5-GPRASP2 (T735I) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | ARMCX5-GPRASP2, GPRASP1 (R802K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (P1208L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (D561G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A311T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (D1269V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (D1388N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A96T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (R286K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (V219I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (R75C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (S123I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (W272C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (T1029R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARMCX5-GPRASP2, GPRASP1 (M1299T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (P1112T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (M603T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (V127L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (T516S) | Single nucleotide variant (missense variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | ARMCX5-GPRASP2, GPRASP1 (M370L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (G816W) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (R1222H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (W585S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (G966E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A889V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (G551V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (A564G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (G721E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (C1241F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (K386Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (V560A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMCX5-GPRASP2, GPRASP1 (V66D) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | ARMCX5-GPRASP2, GPRASP1 (R595G) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | ARMCX5-GPRASP2, GPRASP1 (L791P) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | ARMCX5-GPRASP2, GPRASP1 (P1036S) | Single nucleotide variant (missense variant +1 more) | Intellectual disability | |
| | ARMCX5-GPRASP2, GPRASP1 (P1252T) | Single nucleotide variant (missense variant +1 more) | Intellectual disability | |
| | ARMCX5-GPRASP2, GPRASP1 (E1127Q) | Single nucleotide variant (missense variant +1 more) | Intellectual disability | |