Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08000 | A08 | 7277689 | C | T | downstream_gene_variant | MODIFIER | c.*2887G>A| |
S15 S156 S3 S34 S6 |
2 | BAA08g08000 | A08 | 7280874 | C | T | missense_variant | MODERATE | c.1346G>A|p.Gly449Asp |
S302 |
3 | BAA08g08000 | A08 | 7282311 | C | T | missense_variant | MODERATE | c.305G>A|p.Arg102Gln |
S167 |
4 | BAA08g08000 | A08 | 7282430 | C | T | synonymous_variant | LOW | c.186G>A|p.Val62Val |
S270 |
5 | BAA08g08000 | A08 | 7282515 | C | T | synonymous_variant | LOW | c.171G>A|p.Leu57Leu |
S148 S30 S31 |
6 | BAA08g08000 | A08 | 7282679 | C | T | missense_variant | MODERATE | c.7G>A|p.Asp3Asn |
S118 |
7 | BAA08g08000 | A08 | 7283046 | G | A | upstream_gene_variant | MODIFIER | c.-361C>T| |
S139 |
8 | BAA08g08000 | A08 | 7283180 | C | T | upstream_gene_variant | MODIFIER | c.-495G>A| |
S176 |
9 | BAA08g08000 | A08 | 7284654 | G | A | upstream_gene_variant | MODIFIER | c.-1969C>T| |
S190 |
10 | BAA08g08000 | A08 | 7284802 | G | A | upstream_gene_variant | MODIFIER | c.-2117C>T| |
S174 |
11 | BAA08g08000 | A08 | 7284837 | G | A | upstream_gene_variant | MODIFIER | c.-2152C>T| |
S288 |
12 | BAA08g08000 | A08 | 7285036 | G | A | upstream_gene_variant | MODIFIER | c.-2351C>T| |
S286 |
13 | BAA08g08000 | A08 | 7286626 | C | T | upstream_gene_variant | MODIFIER | c.-3941G>A| |
S236 |
14 | BAA08g08000 | A08 | 7287010 | T | C | upstream_gene_variant | MODIFIER | c.-4325A>G| |
S187 |
15 | BAA08g08000 | A08 | 7287618 | G | A | upstream_gene_variant | MODIFIER | c.-4933C>T| |
S282 |