Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10180 | A02 | 4520651 | G | A | missense_variant | MODERATE | c.2369C>T|p.Ala790Val |
S164 |
2 | BAA02g10180 | A02 | 4523395 | G | A | synonymous_variant | LOW | c.1620C>T|p.Pro540Pro |
S48 |
3 | BAA02g10180 | A02 | 4524169 | C | T | splice_region_variant&synonymous_variant | LOW | c.1113G>A|p.Ser371Ser |
S178 |
4 | BAA02g10180 | A02 | 4524542 | C | T | missense_variant | MODERATE | c.908G>A|p.Ser303Asn |
S25 |
5 | BAA02g10180 | A02 | 4525364 | G | A | missense_variant | MODERATE | c.404C>T|p.Ala135Val |
S125 |
6 | BAA02g10180 | A02 | 4525428 | C | T | missense_variant | MODERATE | c.340G>A|p.Ala114Thr |
S221 |
7 | BAA02g10180 | A02 | 4526118 | G | A | upstream_gene_variant | MODIFIER | c.-55C>T| |
S43 |
8 | BAA02g10180 | A02 | 4528311 | G | A | upstream_gene_variant | MODIFIER | c.-2248C>T| |
S188 |
9 | BAA02g10180 | A02 | 4529291 | C | T | upstream_gene_variant | MODIFIER | c.-3228G>A| |
S278 |
10 | BAA02g10180 | A02 | 4530664 | C | T | upstream_gene_variant | MODIFIER | c.-4601G>A| |
S120 |