Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18700 | A01 | 9188625 | G | A | upstream_gene_variant | MODIFIER | c.-4739G>A| |
S244 |
2 | BAA01g18700 | A01 | 9189396 | C | T | upstream_gene_variant | MODIFIER | c.-3968C>T| |
S7 |
3 | BAA01g18700 | A01 | 9189428 | C | T | upstream_gene_variant | MODIFIER | c.-3936C>T| |
S228 |
4 | BAA01g18700 | A01 | 9192803 | C | T | upstream_gene_variant | MODIFIER | c.-561C>T| |
S146 |
5 | BAA01g18700 | A01 | 9193112 | C | T | upstream_gene_variant | MODIFIER | c.-252C>T| |
S134 |
6 | BAA01g18700 | A01 | 9193601 | C | T | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S206 S26 |
7 | BAA01g18700 | A01 | 9193863 | C | T | missense_variant | MODERATE | c.500C>T|p.Thr167Ile |
S277 |
8 | BAA01g18700 | A01 | 9194330 | G | A | splice_region_variant&intron_variant | LOW | c.868-4G>A| |
S86 |
9 | BAA01g18700 | A01 | 9195288 | C | T | intron_variant | MODIFIER | c.1432-20C>T| |
S128 |
10 | BAA01g18700 | A01 | 9195650 | C | T | intron_variant | MODIFIER | c.1638+30C>T| |
S267 |
11 | BAA01g18700 | A01 | 9195814 | G | A | intron_variant | MODIFIER | c.1729+15G>A| |
S116 |
12 | BAA01g18700 | A01 | 9195915 | G | A | missense_variant | MODERATE | c.1744G>A|p.Asp582Asn |
S240 |
13 | BAA01g18700 | A01 | 9198119 | G | A | downstream_gene_variant | MODIFIER | c.*1070G>A| |
S123 |
14 | BAA01g18700 | A01 | 9198189 | G | A | downstream_gene_variant | MODIFIER | c.*1140G>A| |
S159 S243 |
15 | BAA01g18700 | A01 | 9198786 | G | A | downstream_gene_variant | MODIFIER | c.*1737G>A| |
S59 |