Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18540 | A02 | 9449865 | G | A | upstream_gene_variant | MODIFIER | c.-2437G>A| |
S193 |
2 | BAA02g18540 | A02 | 9449889 | C | T | upstream_gene_variant | MODIFIER | c.-2413C>T| |
S301 S304 |
3 | BAA02g18540 | A02 | 9451158 | C | T | upstream_gene_variant | MODIFIER | c.-1144C>T| |
S182 |
4 | BAA02g18540 | A02 | 9451881 | C | T | upstream_gene_variant | MODIFIER | c.-421C>T| |
S93 |
5 | BAA02g18540 | A02 | 9452108 | C | T | upstream_gene_variant | MODIFIER | c.-194C>T| |
S266 |
6 | BAA02g18540 | A02 | 9452556 | C | T | synonymous_variant | LOW | c.255C>T|p.Asp85Asp |
S189 S226 S250 S41 |
7 | BAA02g18540 | A02 | 9452760 | T | A | missense_variant | MODERATE | c.459T>A|p.Asp153Glu |
S216 |
8 | BAA02g18540 | A02 | 9454019 | C | T | intron_variant | MODIFIER | c.754+964C>T| |
S293 |
9 | BAA02g18540 | A02 | 9455271 | G | A | intron_variant | MODIFIER | c.754+2216G>A| |
S157 S166 |
10 | BAA02g18540 | A02 | 9456449 | C | T | intron_variant | MODIFIER | c.754+3394C>T| |
S100 |
11 | BAA02g18540 | A02 | 9456561 | C | T | intron_variant | MODIFIER | c.755-3331C>T| |
S84 S93 |
12 | BAA02g18540 | A02 | 9457803 | C | T | intron_variant | MODIFIER | c.755-2089C>T| |
S277 |
13 | BAA02g18540 | A02 | 9457857 | G | A | intron_variant | MODIFIER | c.755-2035G>A| |
S193 |
14 | BAA02g18540 | A02 | 9458238 | G | A | intron_variant | MODIFIER | c.755-1654G>A| |
S86 |
15 | BAA02g18540 | A02 | 9459891 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.755-1G>A| |
S232 |
16 | BAA02g18540 | A02 | 9460240 | C | T | missense_variant | MODERATE | c.1103C>T|p.Ala368Val |
S2 |