Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43470 | A02 | 36003562 | C | T | upstream_gene_variant | MODIFIER | c.-4156C>T| |
S167 |
2 | BAA02g43470 | A02 | 36005000 | A | C | upstream_gene_variant | MODIFIER | c.-2718A>C| |
S128 S148 S157 S162 S173 S210 S233 S266 S302 S33 S47 |
3 | BAA02g43470 | A02 | 36005297 | G | A | upstream_gene_variant | MODIFIER | c.-2421G>A| |
S196 |
4 | BAA02g43470 | A02 | 36005638 | G | A | upstream_gene_variant | MODIFIER | c.-2080G>A| |
S152 |
5 | BAA02g43470 | A02 | 36006029 | C | T | upstream_gene_variant | MODIFIER | c.-1689C>T| |
S234 |
6 | BAA02g43470 | A02 | 36006802 | C | T | upstream_gene_variant | MODIFIER | c.-916C>T| |
S192 |
7 | BAA02g43470 | A02 | 36007071 | C | T | upstream_gene_variant | MODIFIER | c.-647C>T| |
S48 |
8 | BAA02g43470 | A02 | 36007309 | G | A | upstream_gene_variant | MODIFIER | c.-409G>A| |
S246 |
9 | BAA02g43470 | A02 | 36008595 | C | T | synonymous_variant | LOW | c.525C>T|p.Phe175Phe |
S25 S264 |
10 | BAA02g43470 | A02 | 36008714 | A | G | splice_region_variant&intron_variant | LOW | c.543-4A>G| |
S11 |
11 | BAA02g43470 | A02 | 36008840 | C | T | missense_variant | MODERATE | c.665C>T|p.Ala222Val |
S189 |
12 | BAA02g43470 | A02 | 36008945 | C | T | missense_variant | MODERATE | c.770C>T|p.Ala257Val |
S202 |
13 | BAA02g43470 | A02 | 36009848 | G | A | missense_variant | MODERATE | c.1261G>A|p.Gly421Arg |
S35 |