Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34400 | A01 | 23039891 | C | T | missense_variant | MODERATE | c.1474G>A|p.Ala492Thr |
S114 S236 |
2 | BAA01g34400 | A01 | 23040267 | C | T | missense_variant | MODERATE | c.1098G>A|p.Met366Ile |
S286 |
3 | BAA01g34400 | A01 | 23040400 | G | A | missense_variant | MODERATE | c.965C>T|p.Ala322Val |
S95 |
4 | BAA01g34400 | A01 | 23040859 | C | T | synonymous_variant | LOW | c.585G>A|p.Lys195Lys |
S156 |
5 | BAA01g34400 | A01 | 23040887 | A | T | missense_variant | MODERATE | c.557T>A|p.Val186Asp |
S98 |
6 | BAA01g34400 | A01 | 23041197 | C | T | missense_variant | MODERATE | c.247G>A|p.Ala83Thr |
S82 S92 |
7 | BAA01g34400 | A01 | 23041437 | C | T | missense_variant | MODERATE | c.7G>A|p.Ala3Thr |
S282 |
8 | BAA01g34400 | A01 | 23041825 | C | T | upstream_gene_variant | MODIFIER | c.-382G>A| |
S266 |
9 | BAA01g34400 | A01 | 23042205 | C | T | upstream_gene_variant | MODIFIER | c.-762G>A| |
S28 |
10 | BAA01g34400 | A01 | 23042990 | C | A | upstream_gene_variant | MODIFIER | c.-1547G>T| |
S139 |
11 | BAA01g34400 | A01 | 23043289 | C | T | upstream_gene_variant | MODIFIER | c.-1846G>A| |
S198 |
12 | BAA01g34400 | A01 | 23044382 | C | T | upstream_gene_variant | MODIFIER | c.-2939G>A| |
S295 |