Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g25690 | A09 | 16547483 | G | A | upstream_gene_variant | MODIFIER | c.-2808G>A| |
S124 |
2 | BAA09g25690 | A09 | 16549787 | C | T | upstream_gene_variant | MODIFIER | c.-504C>T| |
S294 |
3 | BAA09g25690 | A09 | 16549944 | G | A | upstream_gene_variant | MODIFIER | c.-347G>A| |
S69 |
4 | BAA09g25690 | A09 | 16550828 | G | A | missense_variant | MODERATE | c.461G>A|p.Ser154Asn |
S249 |
5 | BAA09g25690 | A09 | 16551016 | G | A | missense_variant | MODERATE | c.577G>A|p.Gly193Arg |
S127 |
6 | BAA09g25690 | A09 | 16551827 | G | A | missense_variant | MODERATE | c.1163G>A|p.Gly388Asp |
S226 S282 |
7 | BAA09g25690 | A09 | 16551992 | G | A | missense_variant | MODERATE | c.1328G>A|p.Gly443Asp |
S11 |
8 | BAA09g25690 | A09 | 16551994 | C | T | missense_variant | MODERATE | c.1330C>T|p.His444Tyr |
S156 |
9 | BAA09g25690 | A09 | 16552000 | C | T | missense_variant | MODERATE | c.1336C>T|p.Pro446Ser |
S182 |
10 | BAA09g25690 | A09 | 16554295 | G | A | downstream_gene_variant | MODIFIER | c.*1901G>A| |
S166 |
11 | BAA09g25690 | A09 | 16555549 | G | A | downstream_gene_variant | MODIFIER | c.*3155G>A| |
S223 |
12 | BAA09g25690 | A09 | 16556113 | C | T | downstream_gene_variant | MODIFIER | c.*3719C>T| |
S60 |
13 | BAA09g25690 | A09 | 16556410 | C | T | downstream_gene_variant | MODIFIER | c.*4016C>T| |
S183 |