Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g33790 | A08 | 21931120 | G | A | missense_variant | MODERATE | c.1804C>T|p.Pro602Ser |
S66 |
2 | BAA08g33790 | A08 | 21931308 | C | T | splice_region_variant&intron_variant | LOW | c.1621-5G>A| |
S251 |
3 | BAA08g33790 | A08 | 21931429 | G | A | missense_variant | MODERATE | c.1582C>T|p.Pro528Ser |
S13 |
4 | BAA08g33790 | A08 | 21931869 | G | A | missense_variant | MODERATE | c.1142C>T|p.Thr381Ile |
S30 S31 |
5 | BAA08g33790 | A08 | 21932331 | G | A | missense_variant&splice_region_variant | MODERATE | c.868C>T|p.Arg290Trp |
S266 |
6 | BAA08g33790 | A08 | 21932418 | C | T | splice_region_variant&intron_variant | LOW | c.866+6G>A| |
S252 |
7 | BAA08g33790 | A08 | 21933176 | C | T | synonymous_variant | LOW | c.528G>A|p.Arg176Arg |
S161 |
8 | BAA08g33790 | A08 | 21933177 | C | T | missense_variant | MODERATE | c.527G>A|p.Arg176Gln |
S198 |
9 | BAA08g33790 | A08 | 21936623 | C | T | upstream_gene_variant | MODIFIER | c.-1711G>A| |
S128 |
10 | BAA08g33790 | A08 | 21936817 | C | T | upstream_gene_variant | MODIFIER | c.-1905G>A| |
S153 |
11 | BAA08g33790 | A08 | 21938511 | C | T | upstream_gene_variant | MODIFIER | c.-3599G>A| |
S74 |
12 | BAA08g33790 | A08 | 21939380 | G | A | upstream_gene_variant | MODIFIER | c.-4468C>T| |
S289 S290 |