Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36720 | A09 | 44951934 | C | T | stop_gained | HIGH | c.421C>T|p.Gln141* |
S192 |
2 | BAA09g36720 | A09 | 44952233 | G | A | stop_gained | HIGH | c.720G>A|p.Trp240* |
S125 |
3 | BAA09g36720 | A09 | 44952539 | G | A | missense_variant | MODERATE | c.953G>A|p.Gly318Asp |
S203 |
4 | BAA09g36720 | A09 | 44952565 | C | T | missense_variant | MODERATE | c.979C>T|p.Leu327Phe |
S152 |
5 | BAA09g36720 | A09 | 44952687 | G | A | missense_variant | MODERATE | c.1027G>A|p.Gly343Arg |
S42 |
6 | BAA09g36720 | A09 | 44952865 | G | A | missense_variant | MODERATE | c.1205G>A|p.Arg402Lys |
S79 S91 |
7 | BAA09g36720 | A09 | 44953134 | G | A | splice_region_variant&intron_variant | LOW | c.1388-4G>A| |
S305 |
8 | BAA09g36720 | A09 | 44953217 | C | T | synonymous_variant | LOW | c.1467C>T|p.Ala489Ala |
S195 |
9 | BAA09g36720 | A09 | 44954071 | G | A | missense_variant | MODERATE | c.2056G>A|p.Val686Met |
S268 |
10 | BAA09g36720 | A09 | 44954247 | G | A | synonymous_variant | LOW | c.2232G>A|p.Glu744Glu |
S73 S91 |