Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14250 | A02 | 6665917 | G | A | missense_variant | MODERATE | c.30G>A|p.Met10Ile |
S210 S225 |
2 | BAA02g14250 | A02 | 6666104 | G | A | missense_variant | MODERATE | c.217G>A|p.Glu73Lys |
S150 |
3 | BAA02g14250 | A02 | 6666284 | G | A | missense_variant | MODERATE | c.397G>A|p.Glu133Lys |
S170 |
4 | BAA02g14250 | A02 | 6666438 | G | A | missense_variant | MODERATE | c.551G>A|p.Gly184Asp |
S139 |
5 | BAA02g14250 | A02 | 6666568 | C | T | synonymous_variant | LOW | c.681C>T|p.Phe227Phe |
S6 |
6 | BAA02g14250 | A02 | 6666589 | G | A | synonymous_variant | LOW | c.702G>A|p.Gly234Gly |
S155 S211 |
7 | BAA02g14250 | A02 | 6666707 | C | T | missense_variant | MODERATE | c.820C>T|p.Pro274Ser |
S242 |
8 | BAA02g14250 | A02 | 6666939 | A | C | missense_variant | MODERATE | c.1052A>C|p.Asn351Thr |
S125 S153 S175 S225 S257 S268 S279 S41 |
9 | BAA02g14250 | A02 | 6667206 | G | A | missense_variant | MODERATE | c.1319G>A|p.Arg440Lys |
S144 |
10 | BAA02g14250 | A02 | 6667788 | G | A | missense_variant | MODERATE | c.1901G>A|p.Arg634Lys |
S136 |
11 | BAA02g14250 | A02 | 6671483 | C | T | downstream_gene_variant | MODIFIER | c.*3646C>T| |
S272 |