| | CEACAM16, CEACAM16-AS1 (L217M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (S212R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (C201F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (L136S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (K343E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | CEACAM16-related condition | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (L175V) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A160T) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (D182E) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (N385T) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (T337I) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (F244*) | Duplication (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (V338G) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R176C) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16-AS1, CEACAM16 (G340S) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (D276E) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R84W) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (L389S) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A375T) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (E213K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (R193W) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (T319M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (M320T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (R146Q) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CEACAM16, CEACAM16-AS1 (A141P) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (T246M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (R400H) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CEACAM16, CEACAM16-AS1 (L59F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (V406I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CEACAM16, CEACAM16-AS1 (D94V) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (Q287fs) | Deletion (frameshift variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (N216K) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R211C) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (F221Y) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | CEACAM16-AS1, CEACAM16 (V124M) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R400fs) | Deletion (frameshift variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (T159A) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (V124L) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A372T) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A295V) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A375E) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (G168S) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (V219L) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (I107V) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R88C) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (S208N) | Single nucleotide variant (missense variant) | not specified | |
| | CEACAM16, CEACAM16-AS1 (A66T) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | CEACAM16-related condition +1 more | |
| | CEACAM16, CEACAM16-AS1 (D333E) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (L26V) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A375V) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CEACAM16, CEACAM16-AS1 (P28A) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (P366L) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 4B +1 more | GConflicting classifications of pathogenicity |
| | CEACAM16, CEACAM16-AS1 (P31T) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (G222C) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | CEACAM16, CEACAM16-AS1 (Q332*) | Single nucleotide variant (nonsense) | not provided | |
| | CEACAM16, CEACAM16-AS1 (P423L) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (P366R) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (S45L) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R225H) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CEACAM16, CEACAM16-AS1 (I294V) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (V309M) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CEACAM16, CEACAM16-AS1 (A55V) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (E33K) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R225C) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (V253M) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (A2V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | CEACAM16, CEACAM16-AS1 (R192H) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (R150H) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (G197D) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (P31L) | Single nucleotide variant (missense variant) | not provided | |
| | CEACAM16, CEACAM16-AS1 (I24L) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | CEACAM16-related condition +1 more | |
| | CEACAM16, CEACAM16-AS1 (P223T) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |