Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16930 | A08 | 13870063 | C | T | missense_variant | MODERATE | c.110C>T|p.Ala37Val |
S18 |
2 | BAA08g16930 | A08 | 13870311 | G | A | missense_variant | MODERATE | c.272G>A|p.Arg91His |
S275 |
3 | BAA08g16930 | A08 | 13871015 | C | T | missense_variant | MODERATE | c.734C>T|p.Ala245Val |
S152 |
4 | BAA08g16930 | A08 | 13871687 | C | T | synonymous_variant | LOW | c.1101C>T|p.Ser367Ser |
S207 |
5 | BAA08g16930 | A08 | 13872462 | C | T | missense_variant | MODERATE | c.1594C>T|p.Leu532Phe |
S139 |
6 | BAA08g16930 | A08 | 13872629 | C | T | synonymous_variant | LOW | c.1761C>T|p.Asp587Asp |
S249 |
7 | BAA08g16930 | A08 | 13872858 | G | A | splice_region_variant&intron_variant | LOW | c.1985+5G>A| |
S181 |