Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39470 | A09 | 47076683 | C | T | downstream_gene_variant | MODIFIER | c.*2661G>A| |
S184 |
2 | BAA09g39470 | A09 | 47076780 | C | T | downstream_gene_variant | MODIFIER | c.*2564G>A| |
S149 |
3 | BAA09g39470 | A09 | 47077133 | C | T | downstream_gene_variant | MODIFIER | c.*2211G>A| |
S155 S211 |
4 | BAA09g39470 | A09 | 47077610 | C | T | downstream_gene_variant | MODIFIER | c.*1734G>A| |
S30 S31 |
5 | BAA09g39470 | A09 | 47078006 | C | T | downstream_gene_variant | MODIFIER | c.*1338G>A| |
S169 |
6 | BAA09g39470 | A09 | 47078342 | G | A | downstream_gene_variant | MODIFIER | c.*1002C>T| |
S273 |
7 | BAA09g39470 | A09 | 47078851 | C | T | downstream_gene_variant | MODIFIER | c.*493G>A| |
S57 |
8 | BAA09g39470 | A09 | 47079014 | G | A | downstream_gene_variant | MODIFIER | c.*330C>T| |
S81 |
9 | BAA09g39470 | A09 | 47079542 | C | T | synonymous_variant | LOW | c.1386G>A|p.Pro462Pro |
S30 S31 |
10 | BAA09g39470 | A09 | 47079773 | C | T | synonymous_variant | LOW | c.1155G>A|p.Lys385Lys |
S211 S227 |
11 | BAA09g39470 | A09 | 47080559 | G | A | synonymous_variant | LOW | c.369C>T|p.Val123Val |
S149 |
12 | BAA09g39470 | A09 | 47083614 | G | A | upstream_gene_variant | MODIFIER | c.-2687C>T| |
S4 |