Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12400 | A08 | 10822314 | C | T | upstream_gene_variant | MODIFIER | c.-4677C>T| |
S291 |
2 | BAA08g12400 | A08 | 10822539 | C | T | upstream_gene_variant | MODIFIER | c.-4452C>T| |
S251 |
3 | BAA08g12400 | A08 | 10822553 | G | A | upstream_gene_variant | MODIFIER | c.-4438G>A| |
S218 |
4 | BAA08g12400 | A08 | 10822575 | G | A | upstream_gene_variant | MODIFIER | c.-4416G>A| |
S301 S304 |
5 | BAA08g12400 | A08 | 10822787 | C | T | upstream_gene_variant | MODIFIER | c.-4204C>T| |
S18 |
6 | BAA08g12400 | A08 | 10823320 | C | T | upstream_gene_variant | MODIFIER | c.-3671C>T| |
S230 |
7 | BAA08g12400 | A08 | 10824125 | G | A | upstream_gene_variant | MODIFIER | c.-2866G>A| |
S100 |
8 | BAA08g12400 | A08 | 10824582 | C | T | upstream_gene_variant | MODIFIER | c.-2409C>T| |
S215 |
9 | BAA08g12400 | A08 | 10825408 | C | T | upstream_gene_variant | MODIFIER | c.-1583C>T| |
S235 |
10 | BAA08g12400 | A08 | 10827708 | C | T | missense_variant | MODERATE | c.376C>T|p.Pro126Ser |
S44 |
11 | BAA08g12400 | A08 | 10827828 | G | A | splice_region_variant&intron_variant | LOW | c.417-8G>A| |
S165 |
12 | BAA08g12400 | A08 | 10828017 | G | A | missense_variant | MODERATE | c.517G>A|p.Asp173Asn |
S131 S19 |
13 | BAA08g12400 | A08 | 10828023 | G | A | missense_variant | MODERATE | c.523G>A|p.Ala175Thr |
S223 |