Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49830 | A09 | 52986663 | G | A | missense_variant | MODERATE | c.1969C>T|p.Pro657Ser |
S45 |
2 | BAA09g49830 | A09 | 52986723 | G | A | splice_region_variant&intron_variant | LOW | c.1912-3C>T| |
S193 |
3 | BAA09g49830 | A09 | 52986838 | C | T | missense_variant | MODERATE | c.1862G>A|p.Gly621Glu |
S219 S72 |
4 | BAA09g49830 | A09 | 52987648 | C | T | synonymous_variant | LOW | c.1137G>A|p.Gln379Gln |
S163 |
5 | BAA09g49830 | A09 | 52987684 | C | T | stop_gained | HIGH | c.1101G>A|p.Trp367* |
S30 S31 |
6 | BAA09g49830 | A09 | 52987782 | C | T | missense_variant | MODERATE | c.1003G>A|p.Glu335Lys |
S168 |
7 | BAA09g49830 | A09 | 52988772 | G | A | missense_variant | MODERATE | c.182C>T|p.Ala61Val |
S167 |
8 | BAA09g49830 | A09 | 52989039 | C | T | upstream_gene_variant | MODIFIER | c.-86G>A| |
S131 |
9 | BAA09g49830 | A09 | 52989760 | T | G | upstream_gene_variant | MODIFIER | c.-807A>C| |
S97 |
10 | BAA09g49830 | A09 | 52991247 | G | A | upstream_gene_variant | MODIFIER | c.-2294C>T| |
S74 |
11 | BAA09g49830 | A09 | 52991338 | A | G | upstream_gene_variant | MODIFIER | c.-2385T>C| |
S204 |
12 | BAA09g49830 | A09 | 52991696 | G | A | upstream_gene_variant | MODIFIER | c.-2743C>T| |
S200 |
13 | BAA09g49830 | A09 | 52991778 | C | T | upstream_gene_variant | MODIFIER | c.-2825G>A| |
S230 |
14 | BAA09g49830 | A09 | 52992104 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S153 |
15 | BAA09g49830 | A09 | 52992150 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S162 |