| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g19250 | A10 | 17716966 | C | T | missense_variant&splice_region_variant | MODERATE | c.595G>A|p.Asp199Asn |
S37 |
| 2 | BAA10g19250 | A10 | 17718178 | C | T | splice_region_variant&intron_variant | LOW | c.307+3G>A| |
S46 |
| 3 | BAA10g19250 | A10 | 17718223 | C | T | missense_variant | MODERATE | c.265G>A|p.Gly89Arg |
S25 |
| 4 | BAA10g19250 | A10 | 17718230 | C | T | synonymous_variant | LOW | c.258G>A|p.Ala86Ala |
S236 |
| 5 | BAA10g19250 | A10 | 17720337 | C | T | upstream_gene_variant | MODIFIER | c.-1447G>A| |
S156 |
| 6 | BAA10g19250 | A10 | 17720477 | C | T | upstream_gene_variant | MODIFIER | c.-1587G>A| |
S11 |
| 7 | BAA10g19250 | A10 | 17721039 | G | A | upstream_gene_variant | MODIFIER | c.-2149C>T| |
S85 |
| 8 | BAA10g19250 | A10 | 17723274 | C | T | upstream_gene_variant | MODIFIER | c.-4384G>A| |
S262 |