Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19310 | A03 | 8564779 | G | A | synonymous_variant | LOW | c.630G>A|p.Thr210Thr |
S226 |
2 | BAA03g19310 | A03 | 8565030 | T | G | missense_variant | MODERATE | c.881T>G|p.Met294Arg |
S44 |
3 | BAA03g19310 | A03 | 8565059 | C | T | stop_gained | HIGH | c.910C>T|p.Gln304* |
S158 |
4 | BAA03g19310 | A03 | 8565587 | G | A | missense_variant | MODERATE | c.1438G>A|p.Asp480Asn |
S161 |
5 | BAA03g19310 | A03 | 8565730 | C | T | synonymous_variant | LOW | c.1581C>T|p.Val527Val |
S23 |
6 | BAA03g19310 | A03 | 8566472 | A | T | stop_gained | HIGH | c.2323A>T|p.Lys775* |
S252 |
7 | BAA03g19310 | A03 | 8566521 | C | T | missense_variant | MODERATE | c.2372C>T|p.Ala791Val |
S237 |
8 | BAA03g19310 | A03 | 8566809 | C | T | missense_variant | MODERATE | c.2660C>T|p.Thr887Ile |
S272 |
9 | BAA03g19310 | A03 | 8567050 | G | A | intron_variant | MODIFIER | c.2871+30G>A| |
S181 |
10 | BAA03g19310 | A03 | 8567092 | C | T | intron_variant | MODIFIER | c.2872-24C>T| |
S80 |
11 | BAA03g19310 | A03 | 8567310 | C | T | intron_variant | MODIFIER | c.2931+135C>T| |
S170 |
12 | BAA03g19310 | A03 | 8567450 | C | T | intron_variant | MODIFIER | c.2932-79C>T| |
S260 |
13 | BAA03g19310 | A03 | 8567550 | G | A | missense_variant | MODERATE | c.2953G>A|p.Glu985Lys |
S265 |
14 | BAA03g19310 | A03 | 8567809 | C | T | intron_variant | MODIFIER | c.3084+128C>T| |
S208 S93 |
15 | BAA03g19310 | A03 | 8568188 | C | T | intron_variant | MODIFIER | c.3246-38C>T| |
S193 |
16 | BAA03g19310 | A03 | 8569192 | C | T | downstream_gene_variant | MODIFIER | c.*114C>T| |
S16 |
17 | BAA03g19310 | A03 | 8569676 | C | T | downstream_gene_variant | MODIFIER | c.*598C>T| |
S17 |
18 | BAA03g19310 | A03 | 8572580 | G | A | downstream_gene_variant | MODIFIER | c.*3502G>A| |
S63 |
19 | BAA03g19310 | A03 | 8573087 | G | T | downstream_gene_variant | MODIFIER | c.*4009G>T| |
S153 S213 |