Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00070 | Scaffold13 | 4237152 | C | T | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S56 |
2 | BAS13g00070 | Scaffold13 | 4237479 | G | A | upstream_gene_variant | MODIFIER | c.-3398G>A| |
S35 |
3 | BAS13g00070 | Scaffold13 | 4238204 | G | A | upstream_gene_variant | MODIFIER | c.-2673G>A| |
S4 |
4 | BAS13g00070 | Scaffold13 | 4238725 | G | A | upstream_gene_variant | MODIFIER | c.-2152G>A| |
S110 |
5 | BAS13g00070 | Scaffold13 | 4239833 | G | A | upstream_gene_variant | MODIFIER | c.-1044G>A| |
S100 |
6 | BAS13g00070 | Scaffold13 | 4240727 | C | T | upstream_gene_variant | MODIFIER | c.-150C>T| |
S18 |
7 | BAS13g00070 | Scaffold13 | 4241212 | C | T | synonymous_variant | LOW | c.336C>T|p.Asp112Asp |
S115 |
8 | BAS13g00070 | Scaffold13 | 4241523 | A | C | missense_variant | MODERATE | c.454A>C|p.Ser152Arg |
S18 S221 S293 S36 |
9 | BAS13g00070 | Scaffold13 | 4241852 | G | A | missense_variant | MODERATE | c.557G>A|p.Ser186Asn |
S226 |
10 | BAS13g00070 | Scaffold13 | 4241928 | C | T | synonymous_variant | LOW | c.633C>T|p.Thr211Thr |
S262 |
11 | BAS13g00070 | Scaffold13 | 4242017 | G | A | missense_variant | MODERATE | c.722G>A|p.Gly241Glu |
S212 |
12 | BAS13g00070 | Scaffold13 | 4244007 | C | T | downstream_gene_variant | MODIFIER | c.*1486C>T| |
S287 |
13 | BAS13g00070 | Scaffold13 | 4244009 | C | T | downstream_gene_variant | MODIFIER | c.*1488C>T| |
S104 |
14 | BAS13g00070 | Scaffold13 | 4244011 | C | T | downstream_gene_variant | MODIFIER | c.*1490C>T| |
S230 |
15 | BAS13g00070 | Scaffold13 | 4244104 | G | A | downstream_gene_variant | MODIFIER | c.*1583G>A| |
S180 S67 |