Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17840 | A09 | 10729882 | G | A | missense_variant | MODERATE | c.740G>A|p.Gly247Glu |
S142 S143 |
2 | BAA09g17840 | A09 | 10729958 | C | T | splice_region_variant&intron_variant | LOW | c.808+8C>T| |
S173 |
3 | BAA09g17840 | A09 | 10731241 | C | T | synonymous_variant | LOW | c.1156C>T|p.Leu386Leu |
S237 |
4 | BAA09g17840 | A09 | 10731707 | G | A | missense_variant | MODERATE | c.1495G>A|p.Glu499Lys |
S10 S182 |
5 | BAA09g17840 | A09 | 10731761 | C | T | missense_variant | MODERATE | c.1549C>T|p.Leu517Phe |
S48 |
6 | BAA09g17840 | A09 | 10731765 | C | T | missense_variant | MODERATE | c.1553C>T|p.Ser518Phe |
S263 |
7 | BAA09g17840 | A09 | 10733950 | C | T | downstream_gene_variant | MODIFIER | c.*1770C>T| |
S140 |
8 | BAA09g17840 | A09 | 10734776 | G | A | downstream_gene_variant | MODIFIER | c.*2596G>A| |
S124 |
9 | BAA09g17840 | A09 | 10735047 | G | A | downstream_gene_variant | MODIFIER | c.*2867G>A| |
S286 |