Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17860 | A05 | 10134462 | C | T | downstream_gene_variant | MODIFIER | c.*1130G>A| |
S44 |
2 | BAA05g17860 | A05 | 10134505 | G | A | downstream_gene_variant | MODIFIER | c.*1087C>T| |
S241 |
3 | BAA05g17860 | A05 | 10134562 | G | T | downstream_gene_variant | MODIFIER | c.*1030C>A| |
S174 |
4 | BAA05g17860 | A05 | 10136051 | C | T | missense_variant | MODERATE | c.1378G>A|p.Ala460Thr |
S291 |
5 | BAA05g17860 | A05 | 10137175 | C | T | missense_variant | MODERATE | c.502G>A|p.Gly168Arg |
S97 |
6 | BAA05g17860 | A05 | 10138514 | G | A | upstream_gene_variant | MODIFIER | c.-554C>T| |
S173 |
7 | BAA05g17860 | A05 | 10138564 | C | T | upstream_gene_variant | MODIFIER | c.-604G>A| |
S183 S198 |
8 | BAA05g17860 | A05 | 10138833 | C | T | upstream_gene_variant | MODIFIER | c.-873G>A| |
S229 |
9 | BAA05g17860 | A05 | 10138841 | C | T | upstream_gene_variant | MODIFIER | c.-881G>A| |
S262 |
10 | BAA05g17860 | A05 | 10138911 | G | A | upstream_gene_variant | MODIFIER | c.-951C>T| |
S125 |
11 | BAA05g17860 | A05 | 10138959 | G | A | upstream_gene_variant | MODIFIER | c.-999C>T| |
S308 |
12 | BAA05g17860 | A05 | 10138961 | G | A | upstream_gene_variant | MODIFIER | c.-1001C>T| |
S186 |
13 | BAA05g17860 | A05 | 10139370 | C | T | upstream_gene_variant | MODIFIER | c.-1410G>A| |
S9 |