Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10700 | A01 | 4915844 | G | A | missense_variant | MODERATE | c.1139C>T|p.Thr380Met |
S45 |
2 | BAA01g10700 | A01 | 4916964 | G | A | missense_variant | MODERATE | c.398C>T|p.Ser133Phe |
S195 |
3 | BAA01g10700 | A01 | 4917004 | C | T | missense_variant | MODERATE | c.358G>A|p.Gly120Arg |
S44 |
4 | BAA01g10700 | A01 | 4917109 | C | T | missense_variant | MODERATE | c.253G>A|p.Val85Ile |
S210 S225 |
5 | BAA01g10700 | A01 | 4917496 | G | A | synonymous_variant | LOW | c.63C>T|p.Leu21Leu |
S297 |
6 | BAA01g10700 | A01 | 4920841 | G | A | upstream_gene_variant | MODIFIER | c.-3283C>T| |
S149 |
7 | BAA01g10700 | A01 | 4921836 | G | A | upstream_gene_variant | MODIFIER | c.-4278C>T| |
S13 |
8 | BAA01g10700 | A01 | 4922040 | G | A | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S9 |