Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50770 | A09 | 53486600 | C | T | downstream_gene_variant | MODIFIER | c.*1625G>A| |
S293 |
2 | BAA09g50770 | A09 | 53488280 | G | A | missense_variant | MODERATE | c.1244C>T|p.Pro415Leu |
S36 |
3 | BAA09g50770 | A09 | 53488746 | G | A | synonymous_variant | LOW | c.867C>T|p.Gly289Gly |
S190 |
4 | BAA09g50770 | A09 | 53488987 | G | A | synonymous_variant | LOW | c.708C>T|p.Val236Val |
S150 |
5 | BAA09g50770 | A09 | 53489734 | C | T | upstream_gene_variant | MODIFIER | c.-40G>A| |
S121 |
6 | BAA09g50770 | A09 | 53489866 | C | T | upstream_gene_variant | MODIFIER | c.-172G>A| |
S242 |
7 | BAA09g50770 | A09 | 53490615 | G | A | upstream_gene_variant | MODIFIER | c.-921C>T| |
S270 |
8 | BAA09g50770 | A09 | 53493265 | C | T | upstream_gene_variant | MODIFIER | c.-3571G>A| |
S142 |
9 | BAA09g50770 | A09 | 53493947 | G | A | upstream_gene_variant | MODIFIER | c.-4253C>T| |
S48 |