Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41900 | A02 | 34994696 | C | T | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S135 |
2 | BAA02g41900 | A02 | 34994809 | G | A | upstream_gene_variant | MODIFIER | c.-1872G>A| |
S259 |
3 | BAA02g41900 | A02 | 34994925 | C | T | upstream_gene_variant | MODIFIER | c.-1756C>T| |
S237 |
4 | BAA02g41900 | A02 | 34995650 | C | T | upstream_gene_variant | MODIFIER | c.-1031C>T| |
S187 |
5 | BAA02g41900 | A02 | 34996967 | G | A | intron_variant | MODIFIER | c.81-187G>A| |
S60 |
6 | BAA02g41900 | A02 | 34997200 | G | A | missense_variant | MODERATE | c.127G>A|p.Val43Ile |
S27 |
7 | BAA02g41900 | A02 | 34998705 | C | T | missense_variant | MODERATE | c.200C>T|p.Thr67Ile |
S262 |
8 | BAA02g41900 | A02 | 35000314 | G | A | downstream_gene_variant | MODIFIER | c.*45G>A| |
S166 |
9 | BAA02g41900 | A02 | 35001209 | C | T | downstream_gene_variant | MODIFIER | c.*940C>T| |
S15 S153 S156 S213 S3 S34 |
10 | BAA02g41900 | A02 | 35001228 | G | A | downstream_gene_variant | MODIFIER | c.*959G>A| |
S62 |
11 | BAA02g41900 | A02 | 35002407 | C | T | downstream_gene_variant | MODIFIER | c.*2138C>T| |
S178 |