Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05000 | A08 | 3684350 | G | A | upstream_gene_variant | MODIFIER | c.-4734G>A| |
S237 |
2 | BAA08g05000 | A08 | 3686168 | G | A | upstream_gene_variant | MODIFIER | c.-2916G>A| |
S301 S304 |
3 | BAA08g05000 | A08 | 3686206 | G | A | upstream_gene_variant | MODIFIER | c.-2878G>A| |
S81 S85 |
4 | BAA08g05000 | A08 | 3686239 | G | A | upstream_gene_variant | MODIFIER | c.-2845G>A| |
S15 S156 S3 S34 S6 |
5 | BAA08g05000 | A08 | 3686246 | C | T | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S104 S52 |
6 | BAA08g05000 | A08 | 3688280 | G | A | upstream_gene_variant | MODIFIER | c.-804G>A| |
S109 |
7 | BAA08g05000 | A08 | 3688853 | C | T | upstream_gene_variant | MODIFIER | c.-231C>T| |
S236 |
8 | BAA08g05000 | A08 | 3688901 | G | A | upstream_gene_variant | MODIFIER | c.-183G>A| |
S37 |
9 | BAA08g05000 | A08 | 3690245 | A | T | missense_variant | MODERATE | c.448A>T|p.Ile150Leu |
S25 |
10 | BAA08g05000 | A08 | 3690392 | C | T | missense_variant | MODERATE | c.595C>T|p.Pro199Ser |
S192 |
11 | BAA08g05000 | A08 | 3690706 | G | A | downstream_gene_variant | MODIFIER | c.*222G>A| |
S19 |