Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12230 | A08 | 10688486 | C | T | upstream_gene_variant | MODIFIER | c.-209C>T| |
S8 |
2 | BAA08g12230 | A08 | 10689016 | C | T | intron_variant | MODIFIER | c.83-186C>T| |
S255 |
3 | BAA08g12230 | A08 | 10689076 | C | T | intron_variant | MODIFIER | c.83-126C>T| |
S50 |
4 | BAA08g12230 | A08 | 10690183 | C | T | missense_variant | MODERATE | c.484C>T|p.His162Tyr |
S208 S219 |
5 | BAA08g12230 | A08 | 10690465 | C | T | synonymous_variant | LOW | c.684C>T|p.Phe228Phe |
S130 |
6 | BAA08g12230 | A08 | 10690636 | C | T | synonymous_variant | LOW | c.855C>T|p.Ala285Ala |
S76 |
7 | BAA08g12230 | A08 | 10691369 | C | T | synonymous_variant | LOW | c.1084C>T|p.Leu362Leu |
S63 |
8 | BAA08g12230 | A08 | 10691901 | C | T | downstream_gene_variant | MODIFIER | c.*419C>T| |
S255 |
9 | BAA08g12230 | A08 | 10691982 | C | T | downstream_gene_variant | MODIFIER | c.*500C>T| |
S189 |
10 | BAA08g12230 | A08 | 10692497 | C | T | downstream_gene_variant | MODIFIER | c.*1015C>T| |
S36 |
11 | BAA08g12230 | A08 | 10692587 | G | A | downstream_gene_variant | MODIFIER | c.*1105G>A| |
S116 |
12 | BAA08g12230 | A08 | 10692722 | G | A | downstream_gene_variant | MODIFIER | c.*1240G>A| |
S289 S290 |
13 | BAA08g12230 | A08 | 10693741 | G | A | downstream_gene_variant | MODIFIER | c.*2259G>A| |
S199 |
14 | BAA08g12230 | A08 | 10695837 | C | T | downstream_gene_variant | MODIFIER | c.*4355C>T| |
S284 |
15 | BAA08g12230 | A08 | 10695993 | G | A | downstream_gene_variant | MODIFIER | c.*4511G>A| |
S183 |
16 | BAA08g12230 | A08 | 10696078 | C | T | downstream_gene_variant | MODIFIER | c.*4596C>T| |
S79 S84 |
17 | BAA08g12230 | A08 | 10696166 | C | T | downstream_gene_variant | MODIFIER | c.*4684C>T| |
S283 |
18 | BAA08g12230 | A08 | 10696255 | G | A | downstream_gene_variant | MODIFIER | c.*4773G>A| |
S225 S73 |
19 | BAA08g12230 | A08 | 10696269 | G | A | downstream_gene_variant | MODIFIER | c.*4787G>A| |
S61 |