| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g14490 | A06 | 7175558 | C | T | synonymous_variant | LOW | c.1677G>A|p.Arg559Arg |
S176 S97 |
| 2 | BAA06g14490 | A06 | 7176683 | C | T | missense_variant | MODERATE | c.811G>A|p.Asp271Asn |
S244 |
| 3 | BAA06g14490 | A06 | 7177190 | C | T | missense_variant | MODERATE | c.394G>A|p.Glu132Lys |
S60 |
| 4 | BAA06g14490 | A06 | 7177777 | C | T | synonymous_variant | LOW | c.24G>A|p.Val8Val |
S266 |
| 5 | BAA06g14490 | A06 | 7177871 | G | A | upstream_gene_variant | MODIFIER | c.-71C>T| |
S186 |
| 6 | BAA06g14490 | A06 | 7178990 | C | T | upstream_gene_variant | MODIFIER | c.-1190G>A| |
S221 |
| 7 | BAA06g14490 | A06 | 7179050 | C | T | upstream_gene_variant | MODIFIER | c.-1250G>A| |
S298 |
| 8 | BAA06g14490 | A06 | 7181816 | G | A | upstream_gene_variant | MODIFIER | c.-4016C>T| |
S143 |