Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g25010 | A08 | 18151271 | G | A | upstream_gene_variant | MODIFIER | c.-4967G>A| |
S40 S49 |
2 | BAA08g25010 | A08 | 18151715 | C | T | upstream_gene_variant | MODIFIER | c.-4523C>T| |
S201 |
3 | BAA08g25010 | A08 | 18151787 | C | T | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S228 |
4 | BAA08g25010 | A08 | 18152379 | G | A | upstream_gene_variant | MODIFIER | c.-3859G>A| |
S238 |
5 | BAA08g25010 | A08 | 18153125 | C | A | upstream_gene_variant | MODIFIER | c.-3113C>A| |
S180 |
6 | BAA08g25010 | A08 | 18155503 | G | A | upstream_gene_variant | MODIFIER | c.-735G>A| |
S139 |
7 | BAA08g25010 | A08 | 18155780 | C | T | upstream_gene_variant | MODIFIER | c.-458C>T| |
S277 |
8 | BAA08g25010 | A08 | 18156366 | C | T | synonymous_variant | LOW | c.129C>T|p.Phe43Phe |
S69 |
9 | BAA08g25010 | A08 | 18156463 | C | T | missense_variant | MODERATE | c.226C>T|p.Leu76Phe |
S13 |
10 | BAA08g25010 | A08 | 18160913 | C | T | downstream_gene_variant | MODIFIER | c.*4067C>T| |
S19 |
11 | BAA08g25010 | A08 | 18161165 | C | T | downstream_gene_variant | MODIFIER | c.*4319C>T| |
S247 |