Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00030 | A02 | 19147 | G | A | upstream_gene_variant | MODIFIER | c.-2578G>A| |
S295 |
2 | BAA02g00030 | A02 | 19434 | G | A | upstream_gene_variant | MODIFIER | c.-2291G>A| |
S25 |
3 | BAA02g00030 | A02 | 19976 | C | T | upstream_gene_variant | MODIFIER | c.-1749C>T| |
S274 |
4 | BAA02g00030 | A02 | 20352 | C | T | upstream_gene_variant | MODIFIER | c.-1373C>T| |
S66 |
5 | BAA02g00030 | A02 | 20368 | C | T | upstream_gene_variant | MODIFIER | c.-1357C>T| |
S274 |
6 | BAA02g00030 | A02 | 20826 | G | A | upstream_gene_variant | MODIFIER | c.-899G>A| |
S155 S211 |
7 | BAA02g00030 | A02 | 22241 | G | A | missense_variant | MODERATE | c.517G>A|p.Val173Ile |
S139 |
8 | BAA02g00030 | A02 | 22817 | C | T | missense_variant | MODERATE | c.1093C>T|p.Pro365Ser |
S277 |
9 | BAA02g00030 | A02 | 22952 | G | A | missense_variant | MODERATE | c.1228G>A|p.Asp410Asn |
S148 S30 S31 |
10 | BAA02g00030 | A02 | 22970 | G | A | missense_variant | MODERATE | c.1246G>A|p.Glu416Lys |
S10 |
11 | BAA02g00030 | A02 | 23574 | G | A | synonymous_variant | LOW | c.1749G>A|p.Gln583Gln |
S232 |
12 | BAA02g00030 | A02 | 24111 | C | T | synonymous_variant | LOW | c.2199C>T|p.Tyr733Tyr |
S130 |
13 | BAA02g00030 | A02 | 24461 | G | A | missense_variant | MODERATE | c.2549G>A|p.Gly850Glu |
S244 |
14 | BAA02g00030 | A02 | 24672 | G | A | synonymous_variant | LOW | c.2760G>A|p.Pro920Pro |
S266 |
15 | BAA02g00030 | A02 | 26228 | G | A | intron_variant | MODIFIER | c.2814+1502G>A| |
S4 |
16 | BAA02g00030 | A02 | 26437 | G | A | intron_variant | MODIFIER | c.2814+1711G>A| |
S158 |
17 | BAA02g00030 | A02 | 26463 | G | A | intron_variant | MODIFIER | c.2814+1737G>A| |
S149 |
18 | BAA02g00030 | A02 | 27083 | C | T | intron_variant | MODIFIER | c.2815-1379C>T| |
S211 |
19 | BAA02g00030 | A02 | 27367 | C | T | intron_variant | MODIFIER | c.2815-1095C>T| |
S250 |
20 | BAA02g00030 | A02 | 27473 | G | A | intron_variant | MODIFIER | c.2815-989G>A| |
S122 |
21 | BAA02g00030 | A02 | 27563 | C | T | intron_variant | MODIFIER | c.2815-899C>T| |
S123 |
22 | BAA02g00030 | A02 | 28009 | G | A | intron_variant | MODIFIER | c.2815-453G>A| |
S259 |
23 | BAA02g00030 | A02 | 28871 | C | T | synonymous_variant | LOW | c.3117C>T|p.Tyr1039Tyr |
S262 |
24 | BAA02g00030 | A02 | 29234 | G | A | synonymous_variant | LOW | c.3480G>A|p.Glu1160Glu |
S162 |
25 | BAA02g00030 | A02 | 29289 | G | A | missense_variant | MODERATE | c.3535G>A|p.Ala1179Thr |
S59 |