Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g06200 | A06 | 3441963 | C | T | synonymous_variant | LOW | c.1248G>A|p.Thr416Thr |
S259 |
2 | BAA06g06200 | A06 | 3442379 | C | T | missense_variant | MODERATE | c.832G>A|p.Asp278Asn |
S262 |
3 | BAA06g06200 | A06 | 3442385 | C | T | missense_variant | MODERATE | c.826G>A|p.Val276Met |
S279 |
4 | BAA06g06200 | A06 | 3442427 | C | T | missense_variant | MODERATE | c.784G>A|p.Asp262Asn |
S259 |
5 | BAA06g06200 | A06 | 3443123 | A | C | missense_variant | MODERATE | c.304T>G|p.Phe102Val |
S127 S174 S175 S203 S280 S78 |
6 | BAA06g06200 | A06 | 3443142 | G | A | synonymous_variant | LOW | c.285C>T|p.Phe95Phe |
S216 |
7 | BAA06g06200 | A06 | 3445075 | G | A | upstream_gene_variant | MODIFIER | c.-1649C>T| |
S115 |
8 | BAA06g06200 | A06 | 3445543 | G | A | upstream_gene_variant | MODIFIER | c.-2117C>T| |
S169 |
9 | BAA06g06200 | A06 | 3445782 | C | T | upstream_gene_variant | MODIFIER | c.-2356G>A| |
S98 |
10 | BAA06g06200 | A06 | 3445785 | C | T | upstream_gene_variant | MODIFIER | c.-2359G>A| |
S288 |
11 | BAA06g06200 | A06 | 3446239 | C | T | upstream_gene_variant | MODIFIER | c.-2813G>A| |
S96 |