Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26290 | A08 | 18791537 | G | A | downstream_gene_variant | MODIFIER | c.*1320C>T| |
S107 |
2 | BAA08g26290 | A08 | 18794193 | G | A | missense_variant | MODERATE | c.245C>T|p.Thr82Met |
S204 |
3 | BAA08g26290 | A08 | 18794485 | C | T | upstream_gene_variant | MODIFIER | c.-48G>A| |
S169 |
4 | BAA08g26290 | A08 | 18794730 | C | T | upstream_gene_variant | MODIFIER | c.-293G>A| |
S296 |
5 | BAA08g26290 | A08 | 18794924 | G | A | upstream_gene_variant | MODIFIER | c.-487C>T| |
S95 |
6 | BAA08g26290 | A08 | 18795286 | C | T | upstream_gene_variant | MODIFIER | c.-849G>A| |
S99 |
7 | BAA08g26290 | A08 | 18795630 | G | C | upstream_gene_variant | MODIFIER | c.-1193C>G| |
S216 |
8 | BAA08g26290 | A08 | 18796379 | G | A | upstream_gene_variant | MODIFIER | c.-1942C>T| |
S281 |
9 | BAA08g26290 | A08 | 18797261 | G | A | upstream_gene_variant | MODIFIER | c.-2824C>T| |
S136 |
10 | BAA08g26290 | A08 | 18798946 | G | A | upstream_gene_variant | MODIFIER | c.-4509C>T| |
S115 |