| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g08290 | A08 | 7577759 | G | A | missense_variant | MODERATE | c.65G>A|p.Arg22Lys | S260 | 
| 2 | BAA08g08290 | A08 | 7578167 | C | T | stop_gained | HIGH | c.385C>T|p.Gln129* | S140 | 
| 3 | BAA08g08290 | A08 | 7578205 | G | A | missense_variant | MODERATE | c.423G>A|p.Met141Ile | S281 | 
| 4 | BAA08g08290 | A08 | 7579106 | C | T | intron_variant | MODIFIER | c.773+461C>T| | S305 | 
| 5 | BAA08g08290 | A08 | 7580515 | G | A | intron_variant | MODIFIER | c.1011+68G>A| | S159 | 
| 6 | BAA08g08290 | A08 | 7580917 | C | T | intron_variant | MODIFIER | c.1012-212C>T| | S83 S88 | 
| 7 | BAA08g08290 | A08 | 7581439 | C | T | missense_variant | MODERATE | c.1322C>T|p.Ser441Leu | S276 | 
| 8 | BAA08g08290 | A08 | 7582197 | C | T | missense_variant | MODERATE | c.2080C>T|p.Leu694Phe | S281 | 
| 9 | BAA08g08290 | A08 | 7582928 | T | C | intron_variant | MODIFIER | c.2588+135T>C| | S134 | 
| 10 | BAA08g08290 | A08 | 7583330 | G | A | intron_variant | MODIFIER | c.2588+537G>A| | S260 | 
| 11 | BAA08g08290 | A08 | 7583867 | A | T | intron_variant | MODIFIER | c.2589-840A>T| | S286 | 
| 12 | BAA08g08290 | A08 | 7583935 | G | A | intron_variant | MODIFIER | c.2589-772G>A| | S148 S210 | 
| 13 | BAA08g08290 | A08 | 7586069 | G | A | downstream_gene_variant | MODIFIER | c.*904G>A| | S306 S308 | 
| 14 | BAA08g08290 | A08 | 7586351 | G | A | downstream_gene_variant | MODIFIER | c.*1186G>A| | S241 | 
| 15 | BAA08g08290 | A08 | 7587260 | G | A | downstream_gene_variant | MODIFIER | c.*2095G>A| | S240 | 
| 16 | BAA08g08290 | A08 | 7588434 | C | T | downstream_gene_variant | MODIFIER | c.*3269C>T| | S143 | 
| 17 | BAA08g08290 | A08 | 7589565 | C | T | downstream_gene_variant | MODIFIER | c.*4400C>T| | S208 S93 | 
| 18 | BAA08g08290 | A08 | 7590091 | C | T | downstream_gene_variant | MODIFIER | c.*4926C>T| | S178 |