Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26330 | A09 | 17109796 | G | A | missense_variant | MODERATE | c.2270C>T|p.Thr757Ile |
S66 |
2 | BAA09g26330 | A09 | 17110428 | C | T | synonymous_variant | LOW | c.1731G>A|p.Leu577Leu |
S68 |
3 | BAA09g26330 | A09 | 17110895 | C | T | missense_variant | MODERATE | c.1264G>A|p.Gly422Arg |
S76 |
4 | BAA09g26330 | A09 | 17110918 | C | T | missense_variant | MODERATE | c.1241G>A|p.Gly414Asp |
S206 S26 |
5 | BAA09g26330 | A09 | 17111272 | C | T | missense_variant | MODERATE | c.887G>A|p.Arg296Gln |
S182 |
6 | BAA09g26330 | A09 | 17112381 | C | T | synonymous_variant | LOW | c.330G>A|p.Lys110Lys |
S208 S219 |
7 | BAA09g26330 | A09 | 17113106 | C | T | upstream_gene_variant | MODIFIER | c.-332G>A| |
S87 |
8 | BAA09g26330 | A09 | 17113190 | C | T | upstream_gene_variant | MODIFIER | c.-416G>A| |
S192 |
9 | BAA09g26330 | A09 | 17113265 | T | G | upstream_gene_variant | MODIFIER | c.-491A>C| |
S106 S200 S40 S45 |
10 | BAA09g26330 | A09 | 17114050 | C | T | upstream_gene_variant | MODIFIER | c.-1276G>A| |
S3 |
11 | BAA09g26330 | A09 | 17114318 | G | A | upstream_gene_variant | MODIFIER | c.-1544C>T| |
S221 |
12 | BAA09g26330 | A09 | 17114327 | G | A | upstream_gene_variant | MODIFIER | c.-1553C>T| |
S45 |
13 | BAA09g26330 | A09 | 17114452 | C | T | upstream_gene_variant | MODIFIER | c.-1678G>A| |
S36 |
14 | BAA09g26330 | A09 | 17114460 | G | A | upstream_gene_variant | MODIFIER | c.-1686C>T| |
S155 S211 |
15 | BAA09g26330 | A09 | 17114538 | G | A | upstream_gene_variant | MODIFIER | c.-1764C>T| |
S298 |
16 | BAA09g26330 | A09 | 17115315 | G | A | upstream_gene_variant | MODIFIER | c.-2541C>T| |
S289 |
17 | BAA09g26330 | A09 | 17117411 | C | T | upstream_gene_variant | MODIFIER | c.-4637G>A| |
S150 |