Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00510 | A08 | 339482 | C | T | upstream_gene_variant | MODIFIER | c.-2984C>T| |
S6 |
2 | BAA08g00510 | A08 | 340706 | G | A | upstream_gene_variant | MODIFIER | c.-1760G>A| |
S1 |
3 | BAA08g00510 | A08 | 341805 | G | A | upstream_gene_variant | MODIFIER | c.-661G>A| |
S96 |
4 | BAA08g00510 | A08 | 342673 | C | T | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S296 |
5 | BAA08g00510 | A08 | 342927 | C | T | intron_variant | MODIFIER | c.228-39C>T| |
S28 |
6 | BAA08g00510 | A08 | 343021 | G | A | missense_variant | MODERATE | c.283G>A|p.Gly95Arg |
S19 |
7 | BAA08g00510 | A08 | 343859 | C | T | downstream_gene_variant | MODIFIER | c.*381C>T| |
S111 |
8 | BAA08g00510 | A08 | 344330 | G | A | downstream_gene_variant | MODIFIER | c.*852G>A| |
S37 |
9 | BAA08g00510 | A08 | 346537 | G | A | downstream_gene_variant | MODIFIER | c.*3059G>A| |
S192 |
10 | BAA08g00510 | A08 | 346807 | C | T | downstream_gene_variant | MODIFIER | c.*3329C>T| |
S219 |
11 | BAA08g00510 | A08 | 346951 | C | T | downstream_gene_variant | MODIFIER | c.*3473C>T| |
S287 |
12 | BAA08g00510 | A08 | 348047 | T | C | downstream_gene_variant | MODIFIER | c.*4569T>C| |
|