Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23330 | A01 | 11990018 | C | T | downstream_gene_variant | MODIFIER | c.*4645G>A| |
S61 |
2 | BAA01g23330 | A01 | 11991535 | G | A | downstream_gene_variant | MODIFIER | c.*3128C>T| |
S280 |
3 | BAA01g23330 | A01 | 11991577 | C | T | downstream_gene_variant | MODIFIER | c.*3086G>A| |
S136 |
4 | BAA01g23330 | A01 | 11992150 | C | T | downstream_gene_variant | MODIFIER | c.*2513G>A| |
S233 |
5 | BAA01g23330 | A01 | 11993061 | C | T | downstream_gene_variant | MODIFIER | c.*1602G>A| |
S170 |
6 | BAA01g23330 | A01 | 11993379 | C | T | downstream_gene_variant | MODIFIER | c.*1284G>A| |
S183 |
7 | BAA01g23330 | A01 | 11993987 | C | T | downstream_gene_variant | MODIFIER | c.*676G>A| |
S249 |
8 | BAA01g23330 | A01 | 11995077 | G | A | intron_variant | MODIFIER | c.1110+25C>T| |
S149 |
9 | BAA01g23330 | A01 | 11995885 | C | T | synonymous_variant | LOW | c.417G>A|p.Leu139Leu |
S158 |
10 | BAA01g23330 | A01 | 11996203 | C | T | missense_variant | MODERATE | c.287G>A|p.Ser96Asn |
S200 |
11 | BAA01g23330 | A01 | 11996461 | G | A | missense_variant | MODERATE | c.29C>T|p.Thr10Ile |
S217 |
12 | BAA01g23330 | A01 | 11997607 | C | T | upstream_gene_variant | MODIFIER | c.-1118G>A| |
S20 |
13 | BAA01g23330 | A01 | 11999564 | G | A | upstream_gene_variant | MODIFIER | c.-3075C>T| |
S195 |