Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001003786.2 | 1246 | Nonsense Mutation | CGA,TGA | R347* | NP_001003786.1 |
NM_001003787.2 | 1246 | Nonsense Mutation | CGA,TGA | R384* | NP_001003787.1 |
NM_001003788.2 | 1246 | Nonsense Mutation | CGA,TGA | R326* | NP_001003788.1 |
NM_001165969.1 | 1246 | UTR 3 | NP_001159441.1 | ||
NM_001165970.1 | 1246 | UTR 3 | NP_001159442.1 | ||
NM_153335.5 | 1246 | UTR 3 | NP_699166.2 | ||
XM_005257797.2 | 1246 | Nonsense Mutation | CGA,TGA | R376* | XP_005257854.1 |
XM_005257798.2 | 1246 | Nonsense Mutation | CGA,TGA | R355* | XP_005257855.1 |
XM_005257799.2 | 1246 | Nonsense Mutation | CGA,TGA | R326* | XP_005257856.1 |
XM_005257800.2 | 1246 | UTR 3 | XP_005257857.1 | ||
XM_005257801.4 | 1246 | Intron | XP_005257858.1 | ||
XM_005257803.4 | 1246 | Intron | XP_005257860.1 | ||
XM_011525466.2 | 1246 | Silent Mutation | AGC,AGT | S369S | XP_011523768.1 |
XM_011525467.2 | 1246 | Nonsense Mutation | CGA,TGA | R349* | XP_011523769.1 |
XM_017025312.1 | 1246 | UTR 3 | XP_016880801.1 | ||
XM_017025313.1 | 1246 | UTR 3 | XP_016880802.1 | ||
XM_017025314.1 | 1246 | Intron | XP_016880803.1 |