Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g39600 | A03 | 18438581 | G | A | upstream_gene_variant | MODIFIER | c.-362G>A| |
S146 |
2 | BAA03g39600 | A03 | 18439046 | G | A | missense_variant | MODERATE | c.104G>A|p.Arg35His |
S203 |
3 | BAA03g39600 | A03 | 18439069 | G | A | missense_variant | MODERATE | c.127G>A|p.Glu43Lys |
S269 |
4 | BAA03g39600 | A03 | 18439536 | C | T | missense_variant | MODERATE | c.452C>T|p.Thr151Ile |
S293 |
5 | BAA03g39600 | A03 | 18439859 | C | T | splice_region_variant&intron_variant | LOW | c.695+8C>T| |
S255 |
6 | BAA03g39600 | A03 | 18440159 | C | T | missense_variant | MODERATE | c.854C>T|p.Thr285Ile |
S134 |
7 | BAA03g39600 | A03 | 18440584 | C | T | synonymous_variant | LOW | c.1099C>T|p.Leu367Leu |
S55 |
8 | BAA03g39600 | A03 | 18441011 | C | T | missense_variant | MODERATE | c.1526C>T|p.Ser509Phe |
S268 |
9 | BAA03g39600 | A03 | 18443434 | G | A | downstream_gene_variant | MODIFIER | c.*1813G>A| |
S169 |
10 | BAA03g39600 | A03 | 18444934 | C | T | downstream_gene_variant | MODIFIER | c.*3313C>T| |
S280 |