Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14460 | A08 | 12339245 | T | A | downstream_gene_variant | MODIFIER | c.*1719A>T| |
S35 |
2 | BAA08g14460 | A08 | 12340220 | C | T | downstream_gene_variant | MODIFIER | c.*744G>A| |
S249 |
3 | BAA08g14460 | A08 | 12341449 | G | A | missense_variant | MODERATE | c.733C>T|p.Pro245Ser |
S30 |
4 | BAA08g14460 | A08 | 12341661 | G | A | missense_variant | MODERATE | c.521C>T|p.Ala174Val |
S155 S211 |
5 | BAA08g14460 | A08 | 12342000 | C | T | intron_variant | MODIFIER | c.456-274G>A| |
S205 |
6 | BAA08g14460 | A08 | 12343382 | C | T | intron_variant | MODIFIER | c.456-1656G>A| |
S302 |
7 | BAA08g14460 | A08 | 12343591 | C | T | intron_variant | MODIFIER | c.455+1518G>A| |
S308 |
8 | BAA08g14460 | A08 | 12343980 | C | T | intron_variant | MODIFIER | c.455+1129G>A| |
S283 |
9 | BAA08g14460 | A08 | 12344404 | C | T | intron_variant | MODIFIER | c.455+705G>A| |
S52 |
10 | BAA08g14460 | A08 | 12344672 | G | A | intron_variant | MODIFIER | c.455+437C>T| |
S66 |
11 | BAA08g14460 | A08 | 12347299 | C | T | upstream_gene_variant | MODIFIER | c.-1736G>A| |
S47 |
12 | BAA08g14460 | A08 | 12349016 | G | A | upstream_gene_variant | MODIFIER | c.-3453C>T| |
S265 |
13 | BAA08g14460 | A08 | 12349402 | G | A | upstream_gene_variant | MODIFIER | c.-3839C>T| |
S185 |
14 | BAA08g14460 | A08 | 12349857 | C | T | upstream_gene_variant | MODIFIER | c.-4294G>A| |
S284 |