Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19290 | A05 | 11341345 | C | T | downstream_gene_variant | MODIFIER | c.*3840G>A| |
S136 |
2 | BAA05g19290 | A05 | 11341731 | C | T | downstream_gene_variant | MODIFIER | c.*3454G>A| |
S18 |
3 | BAA05g19290 | A05 | 11345385 | C | T | missense_variant | MODERATE | c.1351G>A|p.Ala451Thr |
S143 |
4 | BAA05g19290 | A05 | 11345664 | G | A | synonymous_variant | LOW | c.1158C>T|p.Val386Val |
S245 |
5 | BAA05g19290 | A05 | 11347944 | G | A | intron_variant | MODIFIER | c.42-47C>T| |
S185 |
6 | BAA05g19290 | A05 | 11348518 | G | A | upstream_gene_variant | MODIFIER | c.-419C>T| |
S34 |
7 | BAA05g19290 | A05 | 11348759 | G | A | upstream_gene_variant | MODIFIER | c.-660C>T| |
S173 |
8 | BAA05g19290 | A05 | 11349112 | C | T | upstream_gene_variant | MODIFIER | c.-1013G>A| |
S188 |
9 | BAA05g19290 | A05 | 11350312 | T | C | upstream_gene_variant | MODIFIER | c.-2213A>G| |
S1 S161 S228 S90 |
10 | BAA05g19290 | A05 | 11350813 | C | T | upstream_gene_variant | MODIFIER | c.-2714G>A| |
S223 |
11 | BAA05g19290 | A05 | 11351456 | C | T | upstream_gene_variant | MODIFIER | c.-3357G>A| |
S117 |
12 | BAA05g19290 | A05 | 11352910 | C | T | upstream_gene_variant | MODIFIER | c.-4811G>A| |
S155 |