Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30230 | A02 | 17571795 | G | A | upstream_gene_variant | MODIFIER | c.-4977G>A| |
S34 |
2 | BAA02g30230 | A02 | 17572089 | C | T | upstream_gene_variant | MODIFIER | c.-4683C>T| |
S262 |
3 | BAA02g30230 | A02 | 17572261 | G | A | upstream_gene_variant | MODIFIER | c.-4511G>A| |
S155 S211 |
4 | BAA02g30230 | A02 | 17573215 | C | T | upstream_gene_variant | MODIFIER | c.-3557C>T| |
S201 |
5 | BAA02g30230 | A02 | 17574760 | G | A | upstream_gene_variant | MODIFIER | c.-2012G>A| |
S5 |
6 | BAA02g30230 | A02 | 17576329 | G | A | upstream_gene_variant | MODIFIER | c.-443G>A| |
S228 |
7 | BAA02g30230 | A02 | 17576449 | C | T | upstream_gene_variant | MODIFIER | c.-323C>T| |
S270 |
8 | BAA02g30230 | A02 | 17576675 | C | T | upstream_gene_variant | MODIFIER | c.-97C>T| |
S301 S304 |
9 | BAA02g30230 | A02 | 17576750 | C | T | upstream_gene_variant | MODIFIER | c.-22C>T| |
S15 S3 |
10 | BAA02g30230 | A02 | 17576815 | C | T | missense_variant | MODERATE | c.44C>T|p.Ser15Phe |
S160 |
11 | BAA02g30230 | A02 | 17577403 | G | A | missense_variant | MODERATE | c.632G>A|p.Arg211Lys |
S155 S211 |
12 | BAA02g30230 | A02 | 17577513 | G | A | missense_variant | MODERATE | c.742G>A|p.Glu248Lys |
S251 |
13 | BAA02g30230 | A02 | 17577876 | C | T | splice_region_variant&intron_variant | LOW | c.808-3C>T| |
S275 |
14 | BAA02g30230 | A02 | 17578337 | G | A | splice_region_variant&intron_variant | LOW | c.1182+5G>A| |
S79 S91 |