Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g01120 | A03 | 436843 | G | A | splice_region_variant&intron_variant | LOW | c.40+4G>A| |
S112 |
2 | BAA03g01120 | A03 | 437053 | C | T | missense_variant | MODERATE | c.49C>T|p.Pro17Ser |
S219 S72 |
3 | BAA03g01120 | A03 | 438339 | G | A | missense_variant | MODERATE | c.400G>A|p.Ala134Thr |
S155 S211 |
4 | BAA03g01120 | A03 | 438564 | G | A | missense_variant | MODERATE | c.625G>A|p.Gly209Arg |
S236 |
5 | BAA03g01120 | A03 | 438744 | G | A | missense_variant | MODERATE | c.805G>A|p.Asp269Asn |
S155 S211 |
6 | BAA03g01120 | A03 | 439484 | G | A | intron_variant | MODIFIER | c.1314+138G>A| |
S61 |
7 | BAA03g01120 | A03 | 439586 | G | A | intron_variant | MODIFIER | c.1314+240G>A| |
S143 |
8 | BAA03g01120 | A03 | 439696 | C | T | intron_variant | MODIFIER | c.1314+350C>T| |
S302 |
9 | BAA03g01120 | A03 | 440101 | C | T | intron_variant | MODIFIER | c.1314+755C>T| |
S140 S8 |
10 | BAA03g01120 | A03 | 441153 | G | A | intron_variant | MODIFIER | c.1314+1807G>A| |
S282 |
11 | BAA03g01120 | A03 | 441429 | G | A | intron_variant | MODIFIER | c.1314+2083G>A| |
S226 |
12 | BAA03g01120 | A03 | 441597 | C | T | intron_variant | MODIFIER | c.1315-2088C>T| |
S238 |
13 | BAA03g01120 | A03 | 441831 | G | T | intron_variant | MODIFIER | c.1315-1854G>T| |
S273 |
14 | BAA03g01120 | A03 | 447040 | C | T | missense_variant | MODERATE | c.2276C>T|p.Thr759Ile |
S172 S217 |