Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22630 | A08 | 16951461 | G | A | missense_variant | MODERATE | c.1682C>T|p.Ser561Phe |
S302 |
2 | BAA08g22630 | A08 | 16953120 | G | A | missense_variant | MODERATE | c.1019C>T|p.Ala340Val |
S151 S263 |
3 | BAA08g22630 | A08 | 16953142 | G | A | missense_variant | MODERATE | c.997C>T|p.His333Tyr |
S211 |
4 | BAA08g22630 | A08 | 16953229 | C | T | missense_variant | MODERATE | c.910G>A|p.Gly304Arg |
S156 |
5 | BAA08g22630 | A08 | 16953978 | G | A | missense_variant | MODERATE | c.661C>T|p.Pro221Ser |
S256 |
6 | BAA08g22630 | A08 | 16954286 | C | T | missense_variant | MODERATE | c.353G>A|p.Ser118Asn |
S231 |
7 | BAA08g22630 | A08 | 16955463 | G | A | upstream_gene_variant | MODIFIER | c.-549C>T| |
S305 |
8 | BAA08g22630 | A08 | 16958217 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S30 |
9 | BAA08g22630 | A08 | 16959730 | G | A | upstream_gene_variant | MODIFIER | c.-4816C>T| |
S255 |
10 | BAA08g22630 | A08 | 16959803 | G | A | upstream_gene_variant | MODIFIER | c.-4889C>T| |
S203 |