Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44770 | A03 | 21306159 | G | A | downstream_gene_variant | MODIFIER | c.*1378C>T| |
S47 |
2 | BAA03g44770 | A03 | 21309604 | C | T | missense_variant | MODERATE | c.1045G>A|p.Val349Met |
S204 |
3 | BAA03g44770 | A03 | 21309611 | G | A | synonymous_variant | LOW | c.1038C>T|p.Phe346Phe |
S155 S211 |
4 | BAA03g44770 | A03 | 21309656 | G | A | synonymous_variant | LOW | c.993C>T|p.Ser331Ser |
S112 |
5 | BAA03g44770 | A03 | 21310102 | G | A | missense_variant | MODERATE | c.547C>T|p.Leu183Phe |
S296 |
6 | BAA03g44770 | A03 | 21310217 | G | A | synonymous_variant | LOW | c.432C>T|p.Val144Val |
S167 |
7 | BAA03g44770 | A03 | 21310371 | G | A | missense_variant | MODERATE | c.278C>T|p.Pro93Leu |
S155 |
8 | BAA03g44770 | A03 | 21313722 | G | A | upstream_gene_variant | MODIFIER | c.-3074C>T| |
S292 |
9 | BAA03g44770 | A03 | 21315601 | G | A | upstream_gene_variant | MODIFIER | c.-4953C>T| |
S135 |