Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12040 | A08 | 10556860 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Glu |
S228 |
2 | BAA08g12040 | A08 | 10557143 | C | T | upstream_gene_variant | MODIFIER | c.-140G>A| |
S277 |
3 | BAA08g12040 | A08 | 10560214 | A | G | upstream_gene_variant | MODIFIER | c.-3211T>C| |
S71 |
4 | BAA08g12040 | A08 | 10560281 | C | T | upstream_gene_variant | MODIFIER | c.-3278G>A| |
S94 |
5 | BAA08g12040 | A08 | 10560389 | G | A | upstream_gene_variant | MODIFIER | c.-3386C>T| |
S95 |
6 | BAA08g12040 | A08 | 10560862 | G | A | upstream_gene_variant | MODIFIER | c.-3859C>T| |
S301 S304 |
7 | BAA08g12040 | A08 | 10561427 | G | A | upstream_gene_variant | MODIFIER | c.-4424C>T| |
S187 |
8 | BAA08g12040 | A08 | 10561611 | C | T | upstream_gene_variant | MODIFIER | c.-4608G>A| |
S44 |
9 | BAA08g12040 | A08 | 10561709 | C | T | upstream_gene_variant | MODIFIER | c.-4706G>A| |
S200 |