Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g03010 | Scaffold13 | 24895357 | G | A | downstream_gene_variant | MODIFIER | c.*4723C>T| |
S45 |
2 | BAS13g03010 | Scaffold13 | 24896132 | C | T | downstream_gene_variant | MODIFIER | c.*3948G>A| |
S81 S85 |
3 | BAS13g03010 | Scaffold13 | 24896277 | C | T | downstream_gene_variant | MODIFIER | c.*3803G>A| |
S11 |
4 | BAS13g03010 | Scaffold13 | 24898460 | G | A | downstream_gene_variant | MODIFIER | c.*1620C>T| |
S70 |
5 | BAS13g03010 | Scaffold13 | 24903587 | G | A | intron_variant | MODIFIER | c.1738+613C>T| |
S289 S290 |
6 | BAS13g03010 | Scaffold13 | 24905155 | G | A | intron_variant | MODIFIER | c.924+24C>T| |
S115 |
7 | BAS13g03010 | Scaffold13 | 24905511 | G | A | missense_variant | MODERATE | c.592C>T|p.Leu198Phe |
S164 |
8 | BAS13g03010 | Scaffold13 | 24905552 | G | A | missense_variant | MODERATE | c.551C>T|p.Ala184Val |
S15 S3 |
9 | BAS13g03010 | Scaffold13 | 24906989 | G | A | upstream_gene_variant | MODIFIER | c.-887C>T| |
S281 |
10 | BAS13g03010 | Scaffold13 | 24907162 | G | A | upstream_gene_variant | MODIFIER | c.-1060C>T| |
S164 |
11 | BAS13g03010 | Scaffold13 | 24907685 | G | A | upstream_gene_variant | MODIFIER | c.-1583C>T| |
S38 |
12 | BAS13g03010 | Scaffold13 | 24907831 | C | T | upstream_gene_variant | MODIFIER | c.-1729G>A| |
S160 |
13 | BAS13g03010 | Scaffold13 | 24908934 | G | A | upstream_gene_variant | MODIFIER | c.-2832C>T| |
S98 |
14 | BAS13g03010 | Scaffold13 | 24909583 | G | A | upstream_gene_variant | MODIFIER | c.-3481C>T| |
S168 |
15 | BAS13g03010 | Scaffold13 | 24909746 | G | A | upstream_gene_variant | MODIFIER | c.-3644C>T| |
S164 |