Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g02490 | A07 | 1940955 | C | T | upstream_gene_variant | MODIFIER | c.-4776C>T| |
S144 |
2 | BAA07g02490 | A07 | 1941176 | C | T | upstream_gene_variant | MODIFIER | c.-4555C>T| |
S94 |
3 | BAA07g02490 | A07 | 1941435 | C | A | upstream_gene_variant | MODIFIER | c.-4296C>A| |
S166 |
4 | BAA07g02490 | A07 | 1941472 | G | A | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S257 |
5 | BAA07g02490 | A07 | 1942596 | G | A | upstream_gene_variant | MODIFIER | c.-3135G>A| |
S295 |
6 | BAA07g02490 | A07 | 1943072 | G | A | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S105 S106 |
7 | BAA07g02490 | A07 | 1944299 | C | T | upstream_gene_variant | MODIFIER | c.-1432C>T| |
S306 S308 |
8 | BAA07g02490 | A07 | 1945236 | G | A | upstream_gene_variant | MODIFIER | c.-495G>A| |
S19 |
9 | BAA07g02490 | A07 | 1945333 | C | T | upstream_gene_variant | MODIFIER | c.-398C>T| |
S195 |
10 | BAA07g02490 | A07 | 1946802 | C | T | missense_variant | MODERATE | c.688C>T|p.Arg230Trp |
S187 |
11 | BAA07g02490 | A07 | 1946911 | C | T | missense_variant | MODERATE | c.797C>T|p.Ala266Val |
S77 S82 |