Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39630 | A05 | 38683507 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S69 |
2 | BAA05g39630 | A05 | 38683532 | C | T | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S162 |
3 | BAA05g39630 | A05 | 38684087 | C | T | upstream_gene_variant | MODIFIER | c.-687C>T| |
S132 S137 S138 S215 S237 S288 |
4 | BAA05g39630 | A05 | 38684418 | C | T | upstream_gene_variant | MODIFIER | c.-356C>T| |
S286 |
5 | BAA05g39630 | A05 | 38684659 | C | T | upstream_gene_variant | MODIFIER | c.-115C>T| |
S191 S247 |
6 | BAA05g39630 | A05 | 38684788 | C | T | synonymous_variant | LOW | c.15C>T|p.Phe5Phe |
S144 |
7 | BAA05g39630 | A05 | 38684937 | G | A | missense_variant | MODERATE | c.164G>A|p.Arg55His |
S143 |
8 | BAA05g39630 | A05 | 38685141 | C | T | missense_variant | MODERATE | c.368C>T|p.Ala123Val |
S169 |
9 | BAA05g39630 | A05 | 38686413 | C | T | synonymous_variant | LOW | c.862C>T|p.Leu288Leu |
S13 |