| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g14340 | A08 | 12246051 | C | T | splice_region_variant&intron_variant | LOW | c.1205-8G>A| |
S123 |
| 2 | BAA08g14340 | A08 | 12246134 | G | A | missense_variant | MODERATE | c.1193C>T|p.Ala398Val |
S257 |
| 3 | BAA08g14340 | A08 | 12247277 | C | T | missense_variant | MODERATE | c.788G>A|p.Cys263Tyr |
S139 |
| 4 | BAA08g14340 | A08 | 12247922 | G | A | missense_variant | MODERATE | c.143C>T|p.Ser48Phe |
S20 |
| 5 | BAA08g14340 | A08 | 12247926 | C | T | missense_variant | MODERATE | c.139G>A|p.Val47Ile |
S294 |
| 6 | BAA08g14340 | A08 | 12248505 | G | A | upstream_gene_variant | MODIFIER | c.-441C>T| |
S212 S259 |
| 7 | BAA08g14340 | A08 | 12249015 | G | A | upstream_gene_variant | MODIFIER | c.-951C>T| |
S62 |
| 8 | BAA08g14340 | A08 | 12249577 | G | A | upstream_gene_variant | MODIFIER | c.-1513C>T| |
S170 |
| 9 | BAA08g14340 | A08 | 12249739 | G | A | upstream_gene_variant | MODIFIER | c.-1675C>T| |
S116 |
| 10 | BAA08g14340 | A08 | 12250155 | C | T | upstream_gene_variant | MODIFIER | c.-2091G>A| |
S152 |
| 11 | BAA08g14340 | A08 | 12250423 | C | T | upstream_gene_variant | MODIFIER | c.-2359G>A| |
S157 S163 |
| 12 | BAA08g14340 | A08 | 12250673 | A | G | upstream_gene_variant | MODIFIER | c.-2609T>C| |
S161 |
| 13 | BAA08g14340 | A08 | 12250958 | G | A | upstream_gene_variant | MODIFIER | c.-2894C>T| |
S84 S93 |
| 14 | BAA08g14340 | A08 | 12251050 | C | T | upstream_gene_variant | MODIFIER | c.-2986G>A| |
S208 |
| 15 | BAA08g14340 | A08 | 12252077 | G | A | upstream_gene_variant | MODIFIER | c.-4013C>T| |
S32 |
| 16 | BAA08g14340 | A08 | 12252492 | G | A | upstream_gene_variant | MODIFIER | c.-4428C>T| |
S128 |