Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45900 | A09 | 50900572 | C | T | upstream_gene_variant | MODIFIER | c.-3305C>T| |
S181 |
2 | BAA09g45900 | A09 | 50900743 | C | T | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S297 |
3 | BAA09g45900 | A09 | 50908399 | C | T | intron_variant | MODIFIER | c.517+3220C>T| |
S275 |
4 | BAA09g45900 | A09 | 50908410 | C | T | intron_variant | MODIFIER | c.517+3231C>T| |
S275 |
5 | BAA09g45900 | A09 | 50908528 | C | T | intron_variant | MODIFIER | c.517+3349C>T| |
S109 |
6 | BAA09g45900 | A09 | 50908767 | C | T | intron_variant | MODIFIER | c.518-3483C>T| |
S28 |
7 | BAA09g45900 | A09 | 50908826 | C | T | intron_variant | MODIFIER | c.518-3424C>T| |
S18 |
8 | BAA09g45900 | A09 | 50909053 | C | T | intron_variant | MODIFIER | c.518-3197C>T| |
S251 |
9 | BAA09g45900 | A09 | 50912568 | G | A | missense_variant | MODERATE | c.760G>A|p.Glu254Lys |
S39 |
10 | BAA09g45900 | A09 | 50912833 | G | A | missense_variant | MODERATE | c.886G>A|p.Glu296Lys |
S209 |
11 | BAA09g45900 | A09 | 50913191 | G | A | missense_variant | MODERATE | c.1244G>A|p.Arg415Lys |
S82 S92 |
12 | BAA09g45900 | A09 | 50913703 | G | A | missense_variant | MODERATE | c.1756G>A|p.Ala586Thr |
S167 |
13 | BAA09g45900 | A09 | 50913786 | G | A | synonymous_variant | LOW | c.1839G>A|p.Leu613Leu |
S284 |