Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00530 | A08 | 354274 | G | A | upstream_gene_variant | MODIFIER | c.-2998G>A| |
S279 |
2 | BAA08g00530 | A08 | 354957 | A | G | upstream_gene_variant | MODIFIER | c.-2315A>G| |
S166 |
3 | BAA08g00530 | A08 | 355114 | G | A | upstream_gene_variant | MODIFIER | c.-2158G>A| |
S129 |
4 | BAA08g00530 | A08 | 355453 | G | A | upstream_gene_variant | MODIFIER | c.-1819G>A| |
S40 S49 |
5 | BAA08g00530 | A08 | 355632 | C | T | upstream_gene_variant | MODIFIER | c.-1640C>T| |
S51 |
6 | BAA08g00530 | A08 | 358273 | C | T | missense_variant | MODERATE | c.638C>T|p.Pro213Leu |
S295 |
7 | BAA08g00530 | A08 | 358333 | C | T | missense_variant | MODERATE | c.698C>T|p.Pro233Leu |
S34 |
8 | BAA08g00530 | A08 | 360604 | A | T | downstream_gene_variant | MODIFIER | c.*2225A>T| |
S103 |
9 | BAA08g00530 | A08 | 361301 | C | T | downstream_gene_variant | MODIFIER | c.*2922C>T| |
S294 |
10 | BAA08g00530 | A08 | 362488 | C | T | downstream_gene_variant | MODIFIER | c.*4109C>T| |
S50 |
11 | BAA08g00530 | A08 | 362503 | C | T | downstream_gene_variant | MODIFIER | c.*4124C>T| |
S111 |
12 | BAA08g00530 | A08 | 363269 | G | A | downstream_gene_variant | MODIFIER | c.*4890G>A| |
S249 |