Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20730 | A09 | 12822793 | G | A | upstream_gene_variant | MODIFIER | c.-334G>A| |
S87 |
2 | BAA09g20730 | A09 | 12823198 | G | A | synonymous_variant | LOW | c.72G>A|p.Gln24Gln |
S167 |
3 | BAA09g20730 | A09 | 12823597 | C | T | stop_gained | HIGH | c.121C>T|p.Gln41* |
S43 |
4 | BAA09g20730 | A09 | 12823780 | G | A | missense_variant | MODERATE | c.206G>A|p.Gly69Glu |
S33 |
5 | BAA09g20730 | A09 | 12823791 | C | T | missense_variant | MODERATE | c.217C>T|p.Pro73Ser |
S161 |
6 | BAA09g20730 | A09 | 12824576 | C | T | synonymous_variant | LOW | c.1002C>T|p.Ser334Ser |
S206 S26 |
7 | BAA09g20730 | A09 | 12824862 | G | A | intron_variant | MODIFIER | c.1183+18G>A| |
S209 |
8 | BAA09g20730 | A09 | 12825380 | G | A | synonymous_variant | LOW | c.1380G>A|p.Arg460Arg |
S138 |
9 | BAA09g20730 | A09 | 12825979 | C | T | missense_variant | MODERATE | c.1979C>T|p.Ser660Leu |
S128 |
10 | BAA09g20730 | A09 | 12826280 | C | T | missense_variant | MODERATE | c.2165C>T|p.Ser722Phe |
S177 |
11 | BAA09g20730 | A09 | 12826507 | C | T | synonymous_variant | LOW | c.2392C>T|p.Leu798Leu |
S92 |
12 | BAA09g20730 | A09 | 12826924 | C | T | missense_variant | MODERATE | c.2809C>T|p.Pro937Ser |
S15 S3 |
13 | BAA09g20730 | A09 | 12831180 | G | A | downstream_gene_variant | MODIFIER | c.*1764G>A| |
S124 |