Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g32490 | A07 | 31912897 | C | T | missense_variant | MODERATE | c.1258G>A|p.Glu420Lys |
S159 S243 |
2 | BAA07g32490 | A07 | 31913874 | G | A | synonymous_variant | LOW | c.648C>T|p.His216His |
S259 |
3 | BAA07g32490 | A07 | 31914620 | G | A | synonymous_variant | LOW | c.444C>T|p.Thr148Thr |
S295 |
4 | BAA07g32490 | A07 | 31914934 | G | A | missense_variant | MODERATE | c.130C>T|p.Pro44Ser |
S245 |
5 | BAA07g32490 | A07 | 31914999 | C | T | missense_variant | MODERATE | c.65G>A|p.Gly22Glu |
S123 |
6 | BAA07g32490 | A07 | 31915652 | C | T | upstream_gene_variant | MODIFIER | c.-589G>A| |
S148 S31 |
7 | BAA07g32490 | A07 | 31916155 | C | T | upstream_gene_variant | MODIFIER | c.-1092G>A| |
S301 S304 |
8 | BAA07g32490 | A07 | 31918048 | G | A | upstream_gene_variant | MODIFIER | c.-2985C>T| |
S206 S26 |
9 | BAA07g32490 | A07 | 31919199 | G | A | upstream_gene_variant | MODIFIER | c.-4136C>T| |
S38 |