Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g02120 | Scaffold13 | 17174307 | G | A | downstream_gene_variant | MODIFIER | c.*4910C>T| |
S168 |
2 | BAS13g02120 | Scaffold13 | 17175194 | C | T | downstream_gene_variant | MODIFIER | c.*4023G>A| |
S23 |
3 | BAS13g02120 | Scaffold13 | 17175198 | G | A | downstream_gene_variant | MODIFIER | c.*4019C>T| |
S2 |
4 | BAS13g02120 | Scaffold13 | 17177981 | C | T | downstream_gene_variant | MODIFIER | c.*1236G>A| |
S178 |
5 | BAS13g02120 | Scaffold13 | 17178311 | C | T | downstream_gene_variant | MODIFIER | c.*906G>A| |
S42 |
6 | BAS13g02120 | Scaffold13 | 17178401 | C | T | downstream_gene_variant | MODIFIER | c.*816G>A| |
S178 |
7 | BAS13g02120 | Scaffold13 | 17179216 | C | T | downstream_gene_variant | MODIFIER | c.*1G>A| |
S249 |
8 | BAS13g02120 | Scaffold13 | 17179331 | G | A | synonymous_variant | LOW | c.780C>T|p.Ile260Ile |
S229 |
9 | BAS13g02120 | Scaffold13 | 17179339 | C | T | missense_variant | MODERATE | c.772G>A|p.Val258Ile |
S114 |
10 | BAS13g02120 | Scaffold13 | 17179401 | C | T | missense_variant | MODERATE | c.710G>A|p.Ser237Asn |
S70 |
11 | BAS13g02120 | Scaffold13 | 17179811 | C | T | intron_variant | MODIFIER | c.337-37G>A| |
S139 |
12 | BAS13g02120 | Scaffold13 | 17180918 | C | T | upstream_gene_variant | MODIFIER | c.-649G>A| |
S295 |
13 | BAS13g02120 | Scaffold13 | 17181326 | C | T | upstream_gene_variant | MODIFIER | c.-1057G>A| |
S116 |
14 | BAS13g02120 | Scaffold13 | 17181515 | G | A | upstream_gene_variant | MODIFIER | c.-1246C>T| |
S25 |
15 | BAS13g02120 | Scaffold13 | 17181595 | C | T | upstream_gene_variant | MODIFIER | c.-1326G>A| |
S163 |
16 | BAS13g02120 | Scaffold13 | 17181676 | G | A | upstream_gene_variant | MODIFIER | c.-1407C>T| |
S294 |
17 | BAS13g02120 | Scaffold13 | 17182149 | G | A | upstream_gene_variant | MODIFIER | c.-1880C>T| |
S185 |
18 | BAS13g02120 | Scaffold13 | 17182164 | C | T | upstream_gene_variant | MODIFIER | c.-1895G>A| |
S126 |
19 | BAS13g02120 | Scaffold13 | 17182376 | C | T | upstream_gene_variant | MODIFIER | c.-2107G>A| |
S81 |
20 | BAS13g02120 | Scaffold13 | 17182441 | C | G | upstream_gene_variant | MODIFIER | c.-2172G>C| |
S10 S100 S177 S184 S201 S277 S292 S45 S57 S64 S69 S76 S8 S95 S96 |
21 | BAS13g02120 | Scaffold13 | 17182551 | C | T | upstream_gene_variant | MODIFIER | c.-2282G>A| |
S84 S93 |
22 | BAS13g02120 | Scaffold13 | 17182662 | C | T | upstream_gene_variant | MODIFIER | c.-2393G>A| |
S129 |
23 | BAS13g02120 | Scaffold13 | 17182753 | C | T | upstream_gene_variant | MODIFIER | c.-2484G>A| |
S197 |
24 | BAS13g02120 | Scaffold13 | 17182994 | G | A | upstream_gene_variant | MODIFIER | c.-2725C>T| |
S241 |
25 | BAS13g02120 | Scaffold13 | 17183231 | C | T | upstream_gene_variant | MODIFIER | c.-2962G>A| |
S115 |