Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33580 | A02 | 28726752 | G | A | upstream_gene_variant | MODIFIER | c.-2462G>A| |
S209 |
2 | BAA02g33580 | A02 | 28726908 | C | T | upstream_gene_variant | MODIFIER | c.-2306C>T| |
S121 |
3 | BAA02g33580 | A02 | 28727603 | G | A | upstream_gene_variant | MODIFIER | c.-1611G>A| |
S41 |
4 | BAA02g33580 | A02 | 28727609 | G | A | upstream_gene_variant | MODIFIER | c.-1605G>A| |
S82 S92 |
5 | BAA02g33580 | A02 | 28727850 | C | T | upstream_gene_variant | MODIFIER | c.-1364C>T| |
S128 |
6 | BAA02g33580 | A02 | 28727902 | G | A | upstream_gene_variant | MODIFIER | c.-1312G>A| |
S245 |
7 | BAA02g33580 | A02 | 28728484 | G | A | upstream_gene_variant | MODIFIER | c.-730G>A| |
S188 |
8 | BAA02g33580 | A02 | 28729829 | C | T | stop_gained | HIGH | c.616C>T|p.Gln206* |
S282 |
9 | BAA02g33580 | A02 | 28729954 | C | T | synonymous_variant | LOW | c.741C>T|p.Asp247Asp |
S19 |
10 | BAA02g33580 | A02 | 28730120 | C | T | synonymous_variant | LOW | c.907C>T|p.Leu303Leu |
S121 |
11 | BAA02g33580 | A02 | 28730349 | C | T | missense_variant | MODERATE | c.1136C>T|p.Thr379Ile |
S168 |
12 | BAA02g33580 | A02 | 28730456 | G | A | missense_variant | MODERATE | c.1243G>A|p.Gly415Arg |
S281 |
13 | BAA02g33580 | A02 | 28731606 | C | T | missense_variant | MODERATE | c.2138C>T|p.Thr713Ile |
S264 |
14 | BAA02g33580 | A02 | 28731617 | G | A | missense_variant | MODERATE | c.2149G>A|p.Glu717Lys |
S19 |
15 | BAA02g33580 | A02 | 28735133 | G | A | missense_variant | MODERATE | c.2716G>A|p.Asp906Asn |
S174 |
16 | BAA02g33580 | A02 | 28735648 | G | A | intron_variant | MODIFIER | c.2878+353G>A| |
S155 S211 |
17 | BAA02g33580 | A02 | 28736961 | G | A | intron_variant | MODIFIER | c.2879-772G>A| |
S186 |
18 | BAA02g33580 | A02 | 28737149 | G | A | intron_variant | MODIFIER | c.2879-584G>A| |
S122 |
19 | BAA02g33580 | A02 | 28737161 | G | A | intron_variant | MODIFIER | c.2879-572G>A| |
S211 |
20 | BAA02g33580 | A02 | 28737207 | G | A | intron_variant | MODIFIER | c.2879-526G>A| |
S236 |
21 | BAA02g33580 | A02 | 28737774 | G | A | missense_variant | MODERATE | c.2920G>A|p.Glu974Lys |
S291 |
22 | BAA02g33580 | A02 | 28738037 | C | T | intron_variant | MODIFIER | c.2972-131C>T| |
S40 S49 |
23 | BAA02g33580 | A02 | 28738256 | G | A | synonymous_variant | LOW | c.3060G>A|p.Lys1020Lys |
S176 |
24 | BAA02g33580 | A02 | 28741782 | G | A | missense_variant | MODERATE | c.3178G>A|p.Ala1060Thr |
S199 |
25 | BAA02g33580 | A02 | 28742662 | G | A | downstream_gene_variant | MODIFIER | c.*746G>A| |
S45 |