Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06760 | A07 | 16087253 | G | A | upstream_gene_variant | MODIFIER | c.-4897G>A| |
S295 |
2 | BAA07g06760 | A07 | 16089572 | G | A | upstream_gene_variant | MODIFIER | c.-2578G>A| |
S234 |
3 | BAA07g06760 | A07 | 16091389 | C | T | upstream_gene_variant | MODIFIER | c.-761C>T| |
S34 |
4 | BAA07g06760 | A07 | 16091557 | G | A | upstream_gene_variant | MODIFIER | c.-593G>A| |
S107 |
5 | BAA07g06760 | A07 | 16091681 | C | T | upstream_gene_variant | MODIFIER | c.-469C>T| |
S173 |
6 | BAA07g06760 | A07 | 16091713 | G | A | upstream_gene_variant | MODIFIER | c.-437G>A| |
S262 |
7 | BAA07g06760 | A07 | 16091852 | C | T | upstream_gene_variant | MODIFIER | c.-298C>T| |
S302 |
8 | BAA07g06760 | A07 | 16092116 | C | T | upstream_gene_variant | MODIFIER | c.-34C>T| |
S261 S274 S303 |
9 | BAA07g06760 | A07 | 16092189 | G | A | missense_variant | MODERATE | c.40G>A|p.Glu14Lys |
S171 |
10 | BAA07g06760 | A07 | 16092192 | G | A | missense_variant | MODERATE | c.43G>A|p.Glu15Lys |
S177 |
11 | BAA07g06760 | A07 | 16092372 | C | T | missense_variant | MODERATE | c.223C>T|p.Pro75Ser |
S69 |
12 | BAA07g06760 | A07 | 16092450 | T | C | missense_variant | MODERATE | c.301T>C|p.Tyr101His |
S241 |
13 | BAA07g06760 | A07 | 16092468 | C | T | intron_variant | MODIFIER | c.309+10C>T| |
S205 |
14 | BAA07g06760 | A07 | 16092626 | G | A | stop_gained | HIGH | c.351G>A|p.Trp117* |
S28 |
15 | BAA07g06760 | A07 | 16094076 | G | A | intron_variant | MODIFIER | c.629+1172G>A| |
S33 |
16 | BAA07g06760 | A07 | 16095034 | C | T | intron_variant | MODIFIER | c.630-772C>T| |
S189 |
17 | BAA07g06760 | A07 | 16095932 | C | T | intron_variant | MODIFIER | c.687+69C>T| |
S97 |
18 | BAA07g06760 | A07 | 16095971 | G | A | intron_variant | MODIFIER | c.687+108G>A| |
S172 S217 |
19 | BAA07g06760 | A07 | 16096427 | C | T | intron_variant | MODIFIER | c.688-407C>T| |
S37 |
20 | BAA07g06760 | A07 | 16096908 | G | A | synonymous_variant | LOW | c.762G>A|p.Leu254Leu |
S296 |
21 | BAA07g06760 | A07 | 16096925 | G | A | missense_variant | MODERATE | c.779G>A|p.Arg260His |
S178 |
22 | BAA07g06760 | A07 | 16097004 | C | T | splice_region_variant&intron_variant | LOW | c.850+8C>T| |
S281 |
23 | BAA07g06760 | A07 | 16097896 | G | A | missense_variant | MODERATE | c.1214G>A|p.Arg405His |
S283 |
24 | BAA07g06760 | A07 | 16098220 | C | T | intron_variant | MODIFIER | c.1472-13C>T| |
S55 |
25 | BAA07g06760 | A07 | 16099084 | C | T | intron_variant | MODIFIER | c.2030+30C>T| |
S19 |