Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47410 | A09 | 51725663 | G | A | missense_variant | MODERATE | c.1238C>T|p.Ser413Leu |
S97 |
2 | BAA09g47410 | A09 | 51725743 | G | A | synonymous_variant | LOW | c.1158C>T|p.Phe386Phe |
S225 S73 |
3 | BAA09g47410 | A09 | 51725756 | C | T | missense_variant | MODERATE | c.1145G>A|p.Arg382Lys |
S192 |
4 | BAA09g47410 | A09 | 51726076 | G | A | missense_variant | MODERATE | c.973C>T|p.Leu325Phe |
S167 |
5 | BAA09g47410 | A09 | 51726289 | C | T | missense_variant | MODERATE | c.760G>A|p.Gly254Arg |
S94 |
6 | BAA09g47410 | A09 | 51726465 | C | T | missense_variant | MODERATE | c.584G>A|p.Gly195Glu |
S76 |
7 | BAA09g47410 | A09 | 51726856 | G | A | splice_region_variant&intron_variant | LOW | c.196-3C>T| |
S165 |
8 | BAA09g47410 | A09 | 51729754 | C | T | upstream_gene_variant | MODIFIER | c.-2536G>A| |
S302 |
9 | BAA09g47410 | A09 | 51731295 | G | A | upstream_gene_variant | MODIFIER | c.-4077C>T| |
S233 |
10 | BAA09g47410 | A09 | 51731515 | C | T | upstream_gene_variant | MODIFIER | c.-4297G>A| |
S130 |
11 | BAA09g47410 | A09 | 51731901 | C | T | upstream_gene_variant | MODIFIER | c.-4683G>A| |
S122 |