| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g14490 | A07 | 22092692 | G | A | synonymous_variant | LOW | c.357C>T|p.Phe119Phe |
S278 |
| 2 | BAA07g14490 | A07 | 22092712 | C | T | missense_variant | MODERATE | c.337G>A|p.Gly113Arg |
S18 |
| 3 | BAA07g14490 | A07 | 22093160 | G | A | synonymous_variant | LOW | c.57C>T|p.Cys19Cys |
S219 S72 |
| 4 | BAA07g14490 | A07 | 22094677 | C | T | upstream_gene_variant | MODIFIER | c.-1374G>A| |
S97 |
| 5 | BAA07g14490 | A07 | 22095296 | G | A | upstream_gene_variant | MODIFIER | c.-1993C>T| |
S239 |
| 6 | BAA07g14490 | A07 | 22096272 | C | T | upstream_gene_variant | MODIFIER | c.-2969G>A| |
S1 S90 |
| 7 | BAA07g14490 | A07 | 22096350 | G | A | upstream_gene_variant | MODIFIER | c.-3047C>T| |
S142 S299 |
| 8 | BAA07g14490 | A07 | 22097944 | C | A | upstream_gene_variant | MODIFIER | c.-4641G>T| |
S250 |
| 9 | BAA07g14490 | A07 | 22098001 | C | T | upstream_gene_variant | MODIFIER | c.-4698G>A| |
|