Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g21770 | A05 | 25763200 | C | T | downstream_gene_variant | MODIFIER | c.*4823G>A| |
S53 |
2 | BAA05g21770 | A05 | 25766179 | C | T | downstream_gene_variant | MODIFIER | c.*1844G>A| |
S53 |
3 | BAA05g21770 | A05 | 25767381 | C | T | downstream_gene_variant | MODIFIER | c.*642G>A| |
S17 |
4 | BAA05g21770 | A05 | 25767588 | C | T | downstream_gene_variant | MODIFIER | c.*435G>A| |
S226 |
5 | BAA05g21770 | A05 | 25767631 | C | T | downstream_gene_variant | MODIFIER | c.*392G>A| |
S247 |
6 | BAA05g21770 | A05 | 25768254 | C | T | intron_variant | MODIFIER | c.790-40G>A| |
S19 |
7 | BAA05g21770 | A05 | 25768991 | C | T | missense_variant | MODERATE | c.313G>A|p.Ala105Thr |
S105 S106 |
8 | BAA05g21770 | A05 | 25769183 | C | T | missense_variant | MODERATE | c.121G>A|p.Val41Met |
S180 |
9 | BAA05g21770 | A05 | 25769493 | C | T | upstream_gene_variant | MODIFIER | c.-190G>A| |
S271 |
10 | BAA05g21770 | A05 | 25771069 | C | T | upstream_gene_variant | MODIFIER | c.-1766G>A| |
S104 S105 |
11 | BAA05g21770 | A05 | 25771754 | G | A | upstream_gene_variant | MODIFIER | c.-2451C>T| |
S152 |
12 | BAA05g21770 | A05 | 25771821 | C | T | upstream_gene_variant | MODIFIER | c.-2518G>A| |
S264 |
13 | BAA05g21770 | A05 | 25771935 | C | T | upstream_gene_variant | MODIFIER | c.-2632G>A| |
S59 |
14 | BAA05g21770 | A05 | 25772369 | C | T | upstream_gene_variant | MODIFIER | c.-3066G>A| |
S305 |
15 | BAA05g21770 | A05 | 25772628 | C | T | upstream_gene_variant | MODIFIER | c.-3325G>A| |
S159 S243 S299 |
16 | BAA05g21770 | A05 | 25772823 | G | A | upstream_gene_variant | MODIFIER | c.-3520C>T| |
S129 |