Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g12060 | A06 | 6080314 | G | A | downstream_gene_variant | MODIFIER | c.*2202C>T| |
S207 |
2 | BAA06g12060 | A06 | 6081154 | G | A | downstream_gene_variant | MODIFIER | c.*1362C>T| |
S81 S85 |
3 | BAA06g12060 | A06 | 6083602 | G | A | synonymous_variant | LOW | c.1101C>T|p.Ala367Ala |
S38 |
4 | BAA06g12060 | A06 | 6083884 | G | A | synonymous_variant | LOW | c.819C>T|p.Phe273Phe |
S244 |
5 | BAA06g12060 | A06 | 6083950 | C | T | synonymous_variant | LOW | c.753G>A|p.Lys251Lys |
S177 |
6 | BAA06g12060 | A06 | 6084018 | G | A | missense_variant | MODERATE | c.685C>T|p.Pro229Ser |
S166 |
7 | BAA06g12060 | A06 | 6084058 | G | A | synonymous_variant | LOW | c.645C>T|p.Asn215Asn |
S140 |
8 | BAA06g12060 | A06 | 6084216 | C | T | missense_variant | MODERATE | c.487G>A|p.Gly163Arg |
S216 |
9 | BAA06g12060 | A06 | 6084273 | C | T | missense_variant | MODERATE | c.430G>A|p.Gly144Arg |
S174 |
10 | BAA06g12060 | A06 | 6084407 | G | A | missense_variant | MODERATE | c.296C>T|p.Pro99Leu |
S249 |