| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002944.2 | 7100 | Nonsense Mutation | CGA,TGA | R2269* | NP_002935.2 |
| XM_006715548.3 | 7100 | Nonsense Mutation | CGA,TGA | R2264* | XP_006715611.1 |
| XM_011536049.2 | 7100 | Nonsense Mutation | CGA,TGA | R2279* | XP_011534351.1 |
| XM_011536050.2 | 7100 | Nonsense Mutation | CGA,TGA | R2278* | XP_011534352.1 |
| XM_011536051.2 | 7100 | Nonsense Mutation | CGA,TGA | R2270* | XP_011534353.1 |
| XM_011536052.2 | 7100 | Nonsense Mutation | CGA,TGA | R2265* | XP_011534354.1 |
| XM_011536053.2 | 7100 | Nonsense Mutation | CGA,TGA | R2221* | XP_011534355.1 |
| XM_011536054.2 | 7100 | UTR 3 | XP_011534356.1 | ||
| XM_011536055.2 | 7100 | Intron | XP_011534357.1 | ||
| XM_011536056.2 | 7100 | Intron | XP_011534358.1 | ||
| XM_011536057.2 | 7100 | Intron | XP_011534359.1 | ||
| XM_011536058.2 | 7100 | Intron | XP_011534360.1 | ||
| XM_017011172.1 | 7100 | Nonsense Mutation | CGA,TGA | R2256* | XP_016866661.1 |
| XM_017011173.1 | 7100 | Nonsense Mutation | CGA,TGA | R2255* | XP_016866662.1 |