Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49010 | A09 | 52583202 | C | T | upstream_gene_variant | MODIFIER | c.-4486C>T| |
S108 |
2 | BAA09g49010 | A09 | 52583346 | G | A | upstream_gene_variant | MODIFIER | c.-4342G>A| |
S172 S217 |
3 | BAA09g49010 | A09 | 52583389 | G | A | upstream_gene_variant | MODIFIER | c.-4299G>A| |
S4 |
4 | BAA09g49010 | A09 | 52583487 | G | A | upstream_gene_variant | MODIFIER | c.-4201G>A| |
S39 |
5 | BAA09g49010 | A09 | 52585135 | C | T | upstream_gene_variant | MODIFIER | c.-2553C>T| |
S18 |
6 | BAA09g49010 | A09 | 52585210 | C | T | upstream_gene_variant | MODIFIER | c.-2478C>T| |
S140 |
7 | BAA09g49010 | A09 | 52585304 | G | A | upstream_gene_variant | MODIFIER | c.-2384G>A| |
S116 |
8 | BAA09g49010 | A09 | 52585812 | G | A | upstream_gene_variant | MODIFIER | c.-1876G>A| |
S271 |
9 | BAA09g49010 | A09 | 52589641 | G | A | missense_variant&splice_region_variant | MODERATE | c.976G>A|p.Asp326Asn |
S268 |
10 | BAA09g49010 | A09 | 52589722 | G | A | splice_region_variant&intron_variant | LOW | c.977-8G>A| |
S180 |
11 | BAA09g49010 | A09 | 52591848 | G | A | downstream_gene_variant | MODIFIER | c.*1805G>A| |
S217 S248 |