Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g04850 | A07 | 4071880 | C | T | intron_variant | MODIFIER | c.1419+76G>A| |
S18 |
2 | BAA07g04850 | A07 | 4072060 | C | T | intron_variant | MODIFIER | c.1369-54G>A| |
S161 |
3 | BAA07g04850 | A07 | 4072678 | G | A | missense_variant | MODERATE | c.997C>T|p.Pro333Ser |
S67 |
4 | BAA07g04850 | A07 | 4072816 | C | T | missense_variant | MODERATE | c.859G>A|p.Gly287Ser |
S293 |
5 | BAA07g04850 | A07 | 4073393 | G | A | synonymous_variant | LOW | c.282C>T|p.Ser94Ser |
S226 |
6 | BAA07g04850 | A07 | 4073447 | G | A | synonymous_variant | LOW | c.228C>T|p.Gly76Gly |
S54 |
7 | BAA07g04850 | A07 | 4075059 | G | A | upstream_gene_variant | MODIFIER | c.-1385C>T| |
S240 |