Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46960 | A02 | 38020296 | C | T | downstream_gene_variant | MODIFIER | c.*2738G>A| |
S88 |
2 | BAA02g46960 | A02 | 38021536 | C | T | downstream_gene_variant | MODIFIER | c.*1498G>A| |
S183 S198 |
3 | BAA02g46960 | A02 | 38021625 | C | T | downstream_gene_variant | MODIFIER | c.*1409G>A| |
S76 |
4 | BAA02g46960 | A02 | 38021660 | G | A | downstream_gene_variant | MODIFIER | c.*1374C>T| |
S114 |
5 | BAA02g46960 | A02 | 38021707 | G | A | downstream_gene_variant | MODIFIER | c.*1327C>T| |
S259 |
6 | BAA02g46960 | A02 | 38021827 | C | T | downstream_gene_variant | MODIFIER | c.*1207G>A| |
S203 |
7 | BAA02g46960 | A02 | 38023531 | G | A | missense_variant | MODERATE | c.766C>T|p.Leu256Phe |
S157 S163 |
8 | BAA02g46960 | A02 | 38023703 | C | T | intron_variant | MODIFIER | c.664-70G>A| |
S301 S304 |
9 | BAA02g46960 | A02 | 38027075 | G | A | synonymous_variant | LOW | c.90C>T|p.Leu30Leu |
S161 |
10 | BAA02g46960 | A02 | 38027080 | C | T | missense_variant | MODERATE | c.85G>A|p.Asp29Asn |
S295 |
11 | BAA02g46960 | A02 | 38028235 | C | T | upstream_gene_variant | MODIFIER | c.-1071G>A| |
S295 |
12 | BAA02g46960 | A02 | 38029019 | G | A | upstream_gene_variant | MODIFIER | c.-1855C>T| |
S162 |
13 | BAA02g46960 | A02 | 38029186 | C | T | upstream_gene_variant | MODIFIER | c.-2022G>A| |
S15 S3 |
14 | BAA02g46960 | A02 | 38031720 | C | T | upstream_gene_variant | MODIFIER | c.-4556G>A| |
S249 |