Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00220 | Scaffold13 | 5034508 | G | A | missense_variant | MODERATE | c.1322C>T|p.Ser441Leu |
S107 |
2 | BAS13g00220 | Scaffold13 | 5035503 | C | T | missense_variant | MODERATE | c.709G>A|p.Asp237Asn |
S229 |
3 | BAS13g00220 | Scaffold13 | 5036428 | G | A | missense_variant | MODERATE | c.292C>T|p.Pro98Ser |
S203 |
4 | BAS13g00220 | Scaffold13 | 5036657 | C | T | intron_variant | MODIFIER | c.145-82G>A| |
S118 |
5 | BAS13g00220 | Scaffold13 | 5037291 | C | T | upstream_gene_variant | MODIFIER | c.-116G>A| |
S7 |
6 | BAS13g00220 | Scaffold13 | 5037296 | G | A | upstream_gene_variant | MODIFIER | c.-121C>T| |
S176 |
7 | BAS13g00220 | Scaffold13 | 5038596 | G | A | upstream_gene_variant | MODIFIER | c.-1421C>T| |
S16 S165 |
8 | BAS13g00220 | Scaffold13 | 5038802 | G | A | upstream_gene_variant | MODIFIER | c.-1627C>T| |
S100 |
9 | BAS13g00220 | Scaffold13 | 5039684 | C | T | upstream_gene_variant | MODIFIER | c.-2509G>A| |
S155 S211 |
10 | BAS13g00220 | Scaffold13 | 5039693 | G | A | upstream_gene_variant | MODIFIER | c.-2518C>T| |
S36 |
11 | BAS13g00220 | Scaffold13 | 5040017 | C | T | upstream_gene_variant | MODIFIER | c.-2842G>A| |
S47 |
12 | BAS13g00220 | Scaffold13 | 5040647 | G | A | upstream_gene_variant | MODIFIER | c.-3472C>T| |
S266 |
13 | BAS13g00220 | Scaffold13 | 5040667 | C | T | upstream_gene_variant | MODIFIER | c.-3492G>A| |
S44 |
14 | BAS13g00220 | Scaffold13 | 5040711 | G | A | upstream_gene_variant | MODIFIER | c.-3536C>T| |
S28 |