Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g53490 | A09 | 54714637 | G | A | synonymous_variant | LOW | c.1671C>T|p.Ala557Ala |
S274 S45 |
2 | BAA09g53490 | A09 | 54717218 | G | A | missense_variant | MODERATE | c.977C>T|p.Ser326Phe |
S204 |
3 | BAA09g53490 | A09 | 54718780 | G | A | intron_variant | MODIFIER | c.564-823C>T| |
S180 |
4 | BAA09g53490 | A09 | 54719384 | G | A | intron_variant | MODIFIER | c.564-1427C>T| |
S184 |
5 | BAA09g53490 | A09 | 54719789 | C | T | intron_variant | MODIFIER | c.564-1832G>A| |
S50 |
6 | BAA09g53490 | A09 | 54721506 | C | T | intron_variant | MODIFIER | c.564-3549G>A| |
S237 |
7 | BAA09g53490 | A09 | 54725224 | C | T | missense_variant | MODERATE | c.427G>A|p.Ala143Thr |
S203 S8 |
8 | BAA09g53490 | A09 | 54725449 | G | A | missense_variant | MODERATE | c.202C>T|p.His68Tyr |
S202 |
9 | BAA09g53490 | A09 | 54725539 | G | A | missense_variant | MODERATE | c.112C>T|p.Pro38Ser |
S15 S3 |
10 | BAA09g53490 | A09 | 54725856 | G | A | upstream_gene_variant | MODIFIER | c.-206C>T| |
S39 |
11 | BAA09g53490 | A09 | 54726462 | G | A | upstream_gene_variant | MODIFIER | c.-812C>T| |
S291 |
12 | BAA09g53490 | A09 | 54726876 | G | A | upstream_gene_variant | MODIFIER | c.-1226C>T| |
S132 S137 S215 S89 |
13 | BAA09g53490 | A09 | 54727033 | C | T | upstream_gene_variant | MODIFIER | c.-1383G>A| |
S94 |