Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g03160 | A08 | 2203959 | C | T | upstream_gene_variant | MODIFIER | c.-3088C>T| |
S243 S299 |
2 | BAA08g03160 | A08 | 2204245 | C | T | upstream_gene_variant | MODIFIER | c.-2802C>T| |
S172 S217 |
3 | BAA08g03160 | A08 | 2205347 | C | T | upstream_gene_variant | MODIFIER | c.-1700C>T| |
S261 |
4 | BAA08g03160 | A08 | 2207191 | G | A | missense_variant | MODERATE | c.145G>A|p.Glu49Lys |
S116 |
5 | BAA08g03160 | A08 | 2207769 | C | A | splice_region_variant&intron_variant | LOW | c.275-4C>A| |
S208 S267 S40 S65 S86 S92 |
6 | BAA08g03160 | A08 | 2208075 | C | T | intron_variant | MODIFIER | c.513+64C>T| |
S292 |
7 | BAA08g03160 | A08 | 2208213 | G | A | intron_variant | MODIFIER | c.514-78G>A| |
S158 |
8 | BAA08g03160 | A08 | 2213765 | C | T | synonymous_variant | LOW | c.1945C>T|p.Leu649Leu |
S270 |
9 | BAA08g03160 | A08 | 2214245 | C | T | missense_variant | MODERATE | c.2176C>T|p.Pro726Ser |
S36 |
10 | BAA08g03160 | A08 | 2214475 | C | T | missense_variant | MODERATE | c.2318C>T|p.Ala773Val |
S164 |
11 | BAA08g03160 | A08 | 2217068 | C | T | downstream_gene_variant | MODIFIER | c.*1529C>T| |
S162 |