Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41140 | A06 | 26785437 | G | A | missense_variant | MODERATE | c.343G>A|p.Gly115Arg |
S168 |
2 | BAA06g41140 | A06 | 26785569 | G | A | missense_variant | MODERATE | c.475G>A|p.Glu159Lys |
S56 |
3 | BAA06g41140 | A06 | 26785659 | C | T | missense_variant | MODERATE | c.565C>T|p.Leu189Phe |
S293 |
4 | BAA06g41140 | A06 | 26786266 | G | A | missense_variant | MODERATE | c.739G>A|p.Val247Met |
S25 S264 |
5 | BAA06g41140 | A06 | 26786501 | G | A | missense_variant | MODERATE | c.850G>A|p.Glu284Lys |
S19 |
6 | BAA06g41140 | A06 | 26786817 | G | A | missense_variant | MODERATE | c.1079G>A|p.Gly360Glu |
S120 |
7 | BAA06g41140 | A06 | 26787442 | G | A | missense_variant | MODERATE | c.1399G>A|p.Ala467Thr |
S185 |
8 | BAA06g41140 | A06 | 26787589 | G | A | missense_variant | MODERATE | c.1546G>A|p.Gly516Arg |
S136 |
9 | BAA06g41140 | A06 | 26787638 | G | A | missense_variant | MODERATE | c.1595G>A|p.Arg532Lys |
S151 |
10 | BAA06g41140 | A06 | 26790781 | G | A | downstream_gene_variant | MODIFIER | c.*3076G>A| |
S161 |
11 | BAA06g41140 | A06 | 26791329 | C | T | downstream_gene_variant | MODIFIER | c.*3624C>T| |
S182 |
12 | BAA06g41140 | A06 | 26791567 | C | T | downstream_gene_variant | MODIFIER | c.*3862C>T| |
S48 |
13 | BAA06g41140 | A06 | 26791595 | C | T | downstream_gene_variant | MODIFIER | c.*3890C>T| |
S250 |
14 | BAA06g41140 | A06 | 26792027 | G | A | downstream_gene_variant | MODIFIER | c.*4322G>A| |
S206 S26 |
15 | BAA06g41140 | A06 | 26792286 | G | A | downstream_gene_variant | MODIFIER | c.*4581G>A| |
S305 |