| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g23660 | A05 | 28420852 | C | T | missense_variant | MODERATE | c.407C>T|p.Ser136Leu |
S267 |
| 2 | BAA05g23660 | A05 | 28422917 | A | G | splice_region_variant&intron_variant | LOW | c.1018+4A>G| |
S216 S267 |
| 3 | BAA05g23660 | A05 | 28423400 | G | A | missense_variant | MODERATE | c.1165G>A|p.Asp389Asn |
S11 |
| 4 | BAA05g23660 | A05 | 28423674 | C | T | synonymous_variant | LOW | c.1254C>T|p.Ala418Ala |
S103 |
| 5 | BAA05g23660 | A05 | 28425775 | G | A | missense_variant | MODERATE | c.2459G>A|p.Arg820Lys |
S173 |
| 6 | BAA05g23660 | A05 | 28425996 | C | T | intron_variant | MODIFIER | c.2670+10C>T| |
S242 |