Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g08450 | A06 | 4347253 | C | T | missense_variant | MODERATE | c.776G>A|p.Arg259Gln |
S60 |
2 | BAA06g08450 | A06 | 4347425 | C | T | missense_variant | MODERATE | c.604G>A|p.Glu202Lys |
S216 |
3 | BAA06g08450 | A06 | 4347624 | C | T | missense_variant&splice_region_variant | MODERATE | c.547G>A|p.Glu183Lys |
S240 |
4 | BAA06g08450 | A06 | 4347675 | G | A | missense_variant | MODERATE | c.496C>T|p.Leu166Phe |
S47 |
5 | BAA06g08450 | A06 | 4347876 | G | A | stop_gained | HIGH | c.295C>T|p.Arg99* |
S176 |
6 | BAA06g08450 | A06 | 4348340 | C | T | upstream_gene_variant | MODIFIER | c.-170G>A| |
S210 |
7 | BAA06g08450 | A06 | 4349660 | G | A | upstream_gene_variant | MODIFIER | c.-1490C>T| |
S297 |
8 | BAA06g08450 | A06 | 4351281 | C | T | upstream_gene_variant | MODIFIER | c.-3111G>A| |
S177 |
9 | BAA06g08450 | A06 | 4351911 | C | T | upstream_gene_variant | MODIFIER | c.-3741G>A| |
S281 |
10 | BAA06g08450 | A06 | 4352164 | C | T | upstream_gene_variant | MODIFIER | c.-3994G>A| |
S237 |
11 | BAA06g08450 | A06 | 4352505 | G | A | upstream_gene_variant | MODIFIER | c.-4335C>T| |
S276 |