Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47180 | A09 | 51581558 | C | T | upstream_gene_variant | MODIFIER | c.-1461C>T| |
S94 |
2 | BAA09g47180 | A09 | 51582765 | G | A | upstream_gene_variant | MODIFIER | c.-254G>A| |
S177 |
3 | BAA09g47180 | A09 | 51582916 | G | A | upstream_gene_variant | MODIFIER | c.-103G>A| |
S36 |
4 | BAA09g47180 | A09 | 51583447 | G | A | synonymous_variant | LOW | c.294G>A|p.Lys98Lys |
S2 |
5 | BAA09g47180 | A09 | 51583654 | C | T | missense_variant | MODERATE | c.415C>T|p.Pro139Ser |
S179 |
6 | BAA09g47180 | A09 | 51584193 | C | T | missense_variant | MODERATE | c.638C>T|p.Ala213Val |
S279 |
7 | BAA09g47180 | A09 | 51584542 | C | T | missense_variant | MODERATE | c.734C>T|p.Thr245Ile |
S153 S157 S236 S257 S262 |
8 | BAA09g47180 | A09 | 51584999 | C | T | missense_variant | MODERATE | c.1106C>T|p.Ser369Phe |
S186 |
9 | BAA09g47180 | A09 | 51585493 | G | A | synonymous_variant | LOW | c.1461G>A|p.Gln487Gln |
S82 S92 |
10 | BAA09g47180 | A09 | 51588984 | G | A | downstream_gene_variant | MODIFIER | c.*3326G>A| |
S157 |
11 | BAA09g47180 | A09 | 51589151 | G | A | downstream_gene_variant | MODIFIER | c.*3493G>A| |
S239 |
12 | BAA09g47180 | A09 | 51589175 | C | T | downstream_gene_variant | MODIFIER | c.*3517C>T| |
S261 |
13 | BAA09g47180 | A09 | 51590220 | G | A | downstream_gene_variant | MODIFIER | c.*4562G>A| |
S10 |