Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29660 | A02 | 16998997 | C | T | missense_variant | MODERATE | c.1102G>A|p.Ala368Thr |
S181 |
2 | BAA02g29660 | A02 | 16999083 | C | T | splice_region_variant&intron_variant | LOW | c.1024-8G>A| |
S157 S163 |
3 | BAA02g29660 | A02 | 16999442 | C | T | intron_variant | MODIFIER | c.1024-367G>A| |
S66 |
4 | BAA02g29660 | A02 | 17000090 | C | T | intron_variant | MODIFIER | c.1024-1015G>A| |
S167 |
5 | BAA02g29660 | A02 | 17002581 | C | T | missense_variant | MODERATE | c.449G>A|p.Gly150Glu |
S303 |
6 | BAA02g29660 | A02 | 17003341 | C | T | synonymous_variant | LOW | c.87G>A|p.Val29Val |
S159 S188 S243 S276 S298 S299 |
7 | BAA02g29660 | A02 | 17003831 | G | A | upstream_gene_variant | MODIFIER | c.-404C>T| |
S161 |
8 | BAA02g29660 | A02 | 17003871 | C | T | upstream_gene_variant | MODIFIER | c.-444G>A| |
S286 |
9 | BAA02g29660 | A02 | 17004665 | C | T | upstream_gene_variant | MODIFIER | c.-1238G>A| |
S289 S290 |
10 | BAA02g29660 | A02 | 17005327 | G | A | upstream_gene_variant | MODIFIER | c.-1900C>T| |
S298 |
11 | BAA02g29660 | A02 | 17005580 | G | A | upstream_gene_variant | MODIFIER | c.-2153C>T| |
S36 |
12 | BAA02g29660 | A02 | 17005714 | G | A | upstream_gene_variant | MODIFIER | c.-2287C>T| |
S155 S211 |
13 | BAA02g29660 | A02 | 17005756 | C | T | upstream_gene_variant | MODIFIER | c.-2329G>A| |
S283 |
14 | BAA02g29660 | A02 | 17005854 | G | A | upstream_gene_variant | MODIFIER | c.-2427C>T| |
S70 |
15 | BAA02g29660 | A02 | 17006835 | C | T | upstream_gene_variant | MODIFIER | c.-3408G>A| |
S270 |
16 | BAA02g29660 | A02 | 17007032 | G | A | upstream_gene_variant | MODIFIER | c.-3605C>T| |
S43 |
17 | BAA02g29660 | A02 | 17008071 | G | A | upstream_gene_variant | MODIFIER | c.-4644C>T| |
S129 |
18 | BAA02g29660 | A02 | 17008164 | G | A | upstream_gene_variant | MODIFIER | c.-4737C>T| |
S48 |