Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g32140 | A04 | 29795534 | C | T | missense_variant | MODERATE | c.2182G>A|p.Glu728Lys |
S135 |
2 | BAA04g32140 | A04 | 29796548 | G | A | missense_variant | MODERATE | c.1823C>T|p.Ala608Val |
S35 |
3 | BAA04g32140 | A04 | 29797271 | T | A | missense_variant | MODERATE | c.1454A>T|p.His485Leu |
S248 |
4 | BAA04g32140 | A04 | 29797763 | C | T | missense_variant | MODERATE | c.962G>A|p.Arg321Lys |
S208 S219 |
5 | BAA04g32140 | A04 | 29797899 | C | T | missense_variant | MODERATE | c.826G>A|p.Asp276Asn |
S50 |
6 | BAA04g32140 | A04 | 29799606 | C | T | upstream_gene_variant | MODIFIER | c.-882G>A| |
S10 |
7 | BAA04g32140 | A04 | 29799782 | G | A | upstream_gene_variant | MODIFIER | c.-1058C>T| |
S136 |
8 | BAA04g32140 | A04 | 29803176 | G | A | upstream_gene_variant | MODIFIER | c.-4452C>T| |
S18 |