Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04130 | A09 | 2473436 | C | T | upstream_gene_variant | MODIFIER | c.-4905C>T| |
S171 |
2 | BAA09g04130 | A09 | 2474780 | C | T | upstream_gene_variant | MODIFIER | c.-3561C>T| |
S269 |
3 | BAA09g04130 | A09 | 2475342 | G | A | upstream_gene_variant | MODIFIER | c.-2999G>A| |
S8 |
4 | BAA09g04130 | A09 | 2476256 | G | A | upstream_gene_variant | MODIFIER | c.-2085G>A| |
S51 |
5 | BAA09g04130 | A09 | 2476990 | G | A | upstream_gene_variant | MODIFIER | c.-1351G>A| |
S252 |
6 | BAA09g04130 | A09 | 2477186 | C | T | upstream_gene_variant | MODIFIER | c.-1155C>T| |
S158 |
7 | BAA09g04130 | A09 | 2477470 | C | T | upstream_gene_variant | MODIFIER | c.-871C>T| |
S136 |
8 | BAA09g04130 | A09 | 2478371 | C | T | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S17 S218 S269 |
9 | BAA09g04130 | A09 | 2478893 | G | A | missense_variant | MODERATE | c.409G>A|p.Ala137Thr |
S296 |
10 | BAA09g04130 | A09 | 2479726 | G | A | missense_variant | MODERATE | c.832G>A|p.Gly278Ser |
S74 |
11 | BAA09g04130 | A09 | 2480448 | G | A | missense_variant | MODERATE | c.1123G>A|p.Glu375Lys |
S15 S3 |
12 | BAA09g04130 | A09 | 2484130 | G | A | downstream_gene_variant | MODIFIER | c.*3203G>A| |
S36 |