Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05350 | A07 | 4721279 | C | T | upstream_gene_variant | MODIFIER | c.-4348C>T| |
S272 |
2 | BAA07g05350 | A07 | 4727289 | C | T | missense_variant | MODERATE | c.322C>T|p.Leu108Phe |
S256 |
3 | BAA07g05350 | A07 | 4727745 | G | A | missense_variant | MODERATE | c.688G>A|p.Ala230Thr |
S136 |
4 | BAA07g05350 | A07 | 4727817 | T | G | missense_variant | MODERATE | c.760T>G|p.Phe254Val |
S122 S123 S20 S205 S227 S233 S235 S274 S278 S37 |
5 | BAA07g05350 | A07 | 4727847 | C | T | synonymous_variant | LOW | c.790C>T|p.Leu264Leu |
S133 |
6 | BAA07g05350 | A07 | 4727913 | C | T | intron_variant | MODIFIER | c.798-36C>T| |
S277 |
7 | BAA07g05350 | A07 | 4728475 | G | A | downstream_gene_variant | MODIFIER | c.*59G>A| |
S62 |
8 | BAA07g05350 | A07 | 4728566 | C | T | downstream_gene_variant | MODIFIER | c.*150C>T| |
S53 |
9 | BAA07g05350 | A07 | 4729111 | G | A | downstream_gene_variant | MODIFIER | c.*695G>A| |
S171 |
10 | BAA07g05350 | A07 | 4729205 | C | T | downstream_gene_variant | MODIFIER | c.*789C>T| |
S287 |
11 | BAA07g05350 | A07 | 4729517 | G | A | downstream_gene_variant | MODIFIER | c.*1101G>A| |
S244 |
12 | BAA07g05350 | A07 | 4729643 | C | T | downstream_gene_variant | MODIFIER | c.*1227C>T| |
S139 |
13 | BAA07g05350 | A07 | 4729752 | G | A | downstream_gene_variant | MODIFIER | c.*1336G>A| |
S270 |
14 | BAA07g05350 | A07 | 4730841 | C | T | downstream_gene_variant | MODIFIER | c.*2425C>T| |
S30 S31 |
15 | BAA07g05350 | A07 | 4731414 | C | T | downstream_gene_variant | MODIFIER | c.*2998C>T| |
S79 |
16 | BAA07g05350 | A07 | 4732902 | G | A | downstream_gene_variant | MODIFIER | c.*4486G>A| |
S129 |
17 | BAA07g05350 | A07 | 4733353 | G | A | downstream_gene_variant | MODIFIER | c.*4937G>A| |
S39 |