Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00050 | Scaffold13 | 3110499 | C | T | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S297 |
2 | BAS13g00050 | Scaffold13 | 3112335 | G | A | upstream_gene_variant | MODIFIER | c.-2954G>A| |
S54 |
3 | BAS13g00050 | Scaffold13 | 3112341 | C | T | upstream_gene_variant | MODIFIER | c.-2948C>T| |
S33 |
4 | BAS13g00050 | Scaffold13 | 3112525 | G | A | upstream_gene_variant | MODIFIER | c.-2764G>A| |
S107 S238 |
5 | BAS13g00050 | Scaffold13 | 3112555 | G | A | upstream_gene_variant | MODIFIER | c.-2734G>A| |
S286 |
6 | BAS13g00050 | Scaffold13 | 3112797 | G | A | upstream_gene_variant | MODIFIER | c.-2492G>A| |
S129 S164 |
7 | BAS13g00050 | Scaffold13 | 3113178 | C | G | upstream_gene_variant | MODIFIER | c.-2111C>G| |
S216 S265 S39 |
8 | BAS13g00050 | Scaffold13 | 3113868 | G | A | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S169 S225 |
9 | BAS13g00050 | Scaffold13 | 3114048 | G | A | upstream_gene_variant | MODIFIER | c.-1241G>A| |
S18 |
10 | BAS13g00050 | Scaffold13 | 3114164 | G | A | upstream_gene_variant | MODIFIER | c.-1125G>A| |
S114 |
11 | BAS13g00050 | Scaffold13 | 3114316 | C | T | upstream_gene_variant | MODIFIER | c.-973C>T| |
S240 |
12 | BAS13g00050 | Scaffold13 | 3114367 | G | A | upstream_gene_variant | MODIFIER | c.-922G>A| |
S82 |
13 | BAS13g00050 | Scaffold13 | 3114901 | G | A | upstream_gene_variant | MODIFIER | c.-388G>A| |
S245 |
14 | BAS13g00050 | Scaffold13 | 3114987 | C | T | upstream_gene_variant | MODIFIER | c.-302C>T| |
S158 |
15 | BAS13g00050 | Scaffold13 | 3116102 | G | A | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S306 |
16 | BAS13g00050 | Scaffold13 | 3116164 | C | T | synonymous_variant | LOW | c.465C>T|p.Asn155Asn |
S165 S211 |
17 | BAS13g00050 | Scaffold13 | 3116299 | C | T | synonymous_variant | LOW | c.600C>T|p.Ile200Ile |
S140 |
18 | BAS13g00050 | Scaffold13 | 3116690 | C | T | downstream_gene_variant | MODIFIER | c.*388C>T| |
S47 |
19 | BAS13g00050 | Scaffold13 | 3116708 | G | A | downstream_gene_variant | MODIFIER | c.*406G>A| |
S243 S299 |
20 | BAS13g00050 | Scaffold13 | 3116866 | G | A | downstream_gene_variant | MODIFIER | c.*564G>A| |
S172 S217 |
21 | BAS13g00050 | Scaffold13 | 3116874 | C | T | downstream_gene_variant | MODIFIER | c.*572C>T| |
S235 |
22 | BAS13g00050 | Scaffold13 | 3117079 | C | T | downstream_gene_variant | MODIFIER | c.*777C>T| |
S19 |
23 | BAS13g00050 | Scaffold13 | 3117174 | C | A | downstream_gene_variant | MODIFIER | c.*872C>A| |
S305 |
24 | BAS13g00050 | Scaffold13 | 3117431 | G | A | downstream_gene_variant | MODIFIER | c.*1129G>A| |
S174 |
25 | BAS13g00050 | Scaffold13 | 3118275 | G | A | downstream_gene_variant | MODIFIER | c.*1973G>A| |
S232 |