| | | Insertion (frameshift variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (splice donor variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (splice acceptor variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | LOC126861535, ITGA7 (Q718* +13 more) | Single nucleotide variant (nonsense) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Deletion (frameshift variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Deletion (frameshift variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Duplication (frameshift variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | ITGA7, LOC126861535 (Q646fs +13 more) | Deletion (frameshift variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Deletion (frameshift variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Deletion (frameshift variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (intron variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Indel (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Inversion (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | ITGA7, LOC126861535 (F314L +13 more) | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | ITGA7, LOC126861535 (D259E +12 more) | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | ITGA7, LOC126861535 (I237V +12 more) | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | ITGA7, LOC126861535 (T313A +13 more) | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency +1 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant +3 more) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Deletion | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| | | Single nucleotide variant (synonymous variant) | Congenital muscular dystrophy due to integrin alpha-7 deficiency | |