Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05150 | A08 | 3844258 | G | A | upstream_gene_variant | MODIFIER | c.-3464G>A| |
S94 |
2 | BAA08g05150 | A08 | 3844357 | C | T | upstream_gene_variant | MODIFIER | c.-3365C>T| |
S44 |
3 | BAA08g05150 | A08 | 3844837 | C | T | upstream_gene_variant | MODIFIER | c.-2885C>T| |
S308 |
4 | BAA08g05150 | A08 | 3845839 | G | A | upstream_gene_variant | MODIFIER | c.-1883G>A| |
S281 |
5 | BAA08g05150 | A08 | 3846118 | C | T | upstream_gene_variant | MODIFIER | c.-1604C>T| |
S305 |
6 | BAA08g05150 | A08 | 3846649 | C | T | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S50 |
7 | BAA08g05150 | A08 | 3847437 | C | T | upstream_gene_variant | MODIFIER | c.-285C>T| |
S287 |
8 | BAA08g05150 | A08 | 3848433 | G | A | missense_variant | MODERATE | c.712G>A|p.Ala238Thr |
S247 |
9 | BAA08g05150 | A08 | 3848748 | C | T | missense_variant | MODERATE | c.1027C>T|p.Pro343Ser |
S235 |
10 | BAA08g05150 | A08 | 3852227 | G | A | downstream_gene_variant | MODIFIER | c.*3096G>A| |
S109 |
11 | BAA08g05150 | A08 | 3852555 | G | A | downstream_gene_variant | MODIFIER | c.*3424G>A| |
S301 S304 |
12 | BAA08g05150 | A08 | 3853542 | C | T | downstream_gene_variant | MODIFIER | c.*4411C>T| |
S215 |