Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26860 | A05 | 31387509 | C | T | upstream_gene_variant | MODIFIER | c.-1947C>T| |
S202 |
2 | BAA05g26860 | A05 | 31389352 | G | A | upstream_gene_variant | MODIFIER | c.-104G>A| |
S225 S73 |
3 | BAA05g26860 | A05 | 31389465 | C | T | missense_variant | MODERATE | c.10C>T|p.Leu4Phe |
S208 |
4 | BAA05g26860 | A05 | 31389495 | C | T | missense_variant | MODERATE | c.40C>T|p.Pro14Ser |
S19 |
5 | BAA05g26860 | A05 | 31390982 | G | A | splice_region_variant&intron_variant | LOW | c.719-4G>A| |
S176 S9 |
6 | BAA05g26860 | A05 | 31391047 | C | T | synonymous_variant | LOW | c.780C>T|p.Ala260Ala |
S42 |
7 | BAA05g26860 | A05 | 31391096 | G | A | intron_variant | MODIFIER | c.813+16G>A| |
S1 S90 |
8 | BAA05g26860 | A05 | 31391606 | G | A | missense_variant | MODERATE | c.911G>A|p.Gly304Glu |
S211 S227 |
9 | BAA05g26860 | A05 | 31391805 | G | A | intron_variant | MODIFIER | c.1004+27G>A| |
S9 |
10 | BAA05g26860 | A05 | 31392868 | G | A | synonymous_variant | LOW | c.1332G>A|p.Lys444Lys |
S308 |