Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18460 | A08 | 14770295 | C | T | upstream_gene_variant | MODIFIER | c.-1696C>T| |
S260 |
2 | BAA08g18460 | A08 | 14770297 | C | T | upstream_gene_variant | MODIFIER | c.-1694C>T| |
S47 |
3 | BAA08g18460 | A08 | 14771208 | C | T | upstream_gene_variant | MODIFIER | c.-783C>T| |
S36 |
4 | BAA08g18460 | A08 | 14771439 | C | T | upstream_gene_variant | MODIFIER | c.-552C>T| |
S181 |
5 | BAA08g18460 | A08 | 14772226 | C | T | missense_variant | MODERATE | c.236C>T|p.Ala79Val |
S168 |
6 | BAA08g18460 | A08 | 14772384 | C | T | missense_variant | MODERATE | c.394C>T|p.Pro132Ser |
S166 |
7 | BAA08g18460 | A08 | 14777410 | C | T | downstream_gene_variant | MODIFIER | c.*3327C>T| |
S9 |
8 | BAA08g18460 | A08 | 14777554 | G | A | downstream_gene_variant | MODIFIER | c.*3471G>A| |
S11 |
9 | BAA08g18460 | A08 | 14778561 | G | A | downstream_gene_variant | MODIFIER | c.*4478G>A| |
S56 |
10 | BAA08g18460 | A08 | 14778818 | C | T | downstream_gene_variant | MODIFIER | c.*4735C>T| |
S293 |