Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g05630 | A06 | 3170523 | C | T | missense_variant | MODERATE | c.1498G>A|p.Val500Ile |
S288 |
2 | BAA06g05630 | A06 | 3170692 | G | A | synonymous_variant | LOW | c.1329C>T|p.Leu443Leu |
S155 S211 |
3 | BAA06g05630 | A06 | 3170895 | G | A | missense_variant | MODERATE | c.1126C>T|p.Arg376Cys |
S232 |
4 | BAA06g05630 | A06 | 3170907 | C | T | missense_variant | MODERATE | c.1114G>A|p.Glu372Lys |
S171 |
5 | BAA06g05630 | A06 | 3171115 | C | T | synonymous_variant | LOW | c.906G>A|p.Val302Val |
S247 |
6 | BAA06g05630 | A06 | 3171140 | C | T | missense_variant | MODERATE | c.881G>A|p.Arg294Lys |
S269 |
7 | BAA06g05630 | A06 | 3171558 | C | T | missense_variant | MODERATE | c.463G>A|p.Gly155Arg |
S275 |
8 | BAA06g05630 | A06 | 3171569 | C | T | missense_variant | MODERATE | c.452G>A|p.Gly151Asp |
S209 |
9 | BAA06g05630 | A06 | 3171745 | G | A | synonymous_variant | LOW | c.276C>T|p.Cys92Cys |
S295 |