Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15480 | A09 | 8848173 | G | A | downstream_gene_variant | MODIFIER | c.*1798C>T| |
S70 |
2 | BAA09g15480 | A09 | 8849244 | G | A | downstream_gene_variant | MODIFIER | c.*727C>T| |
S167 |
3 | BAA09g15480 | A09 | 8850090 | G | A | missense_variant | MODERATE | c.1066C>T|p.Pro356Ser |
S25 |
4 | BAA09g15480 | A09 | 8851801 | C | T | intron_variant | MODIFIER | c.304-61G>A| |
S173 |
5 | BAA09g15480 | A09 | 8855035 | C | T | upstream_gene_variant | MODIFIER | c.-2778G>A| |
S297 |
6 | BAA09g15480 | A09 | 8855110 | C | T | upstream_gene_variant | MODIFIER | c.-2853G>A| |
S256 |
7 | BAA09g15480 | A09 | 8855321 | C | T | upstream_gene_variant | MODIFIER | c.-3064G>A| |
S179 |
8 | BAA09g15480 | A09 | 8855322 | C | T | upstream_gene_variant | MODIFIER | c.-3065G>A| |
|
9 | BAA09g15480 | A09 | 8856547 | C | T | upstream_gene_variant | MODIFIER | c.-4290G>A| |
S6 |
10 | BAA09g15480 | A09 | 8856582 | G | A | upstream_gene_variant | MODIFIER | c.-4325C>T| |
S233 |