Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22140 | A08 | 16716119 | C | T | missense_variant | MODERATE | c.2014G>A|p.Glu672Lys |
S250 |
2 | BAA08g22140 | A08 | 16716322 | G | A | missense_variant | MODERATE | c.1811C>T|p.Ser604Phe |
S289 S290 |
3 | BAA08g22140 | A08 | 16716548 | C | T | missense_variant | MODERATE | c.1585G>A|p.Ala529Thr |
S46 |
4 | BAA08g22140 | A08 | 16716676 | C | T | missense_variant | MODERATE | c.1457G>A|p.Arg486His |
S92 |
5 | BAA08g22140 | A08 | 16716704 | C | T | missense_variant | MODERATE | c.1429G>A|p.Val477Met |
S243 |
6 | BAA08g22140 | A08 | 16716911 | G | A | missense_variant | MODERATE | c.1291C>T|p.Leu431Phe |
S85 |
7 | BAA08g22140 | A08 | 16717039 | G | A | missense_variant | MODERATE | c.1163C>T|p.Pro388Leu |
S286 |
8 | BAA08g22140 | A08 | 16717218 | G | A | synonymous_variant | LOW | c.984C>T|p.Thr328Thr |
S202 |
9 | BAA08g22140 | A08 | 16717219 | G | A | missense_variant | MODERATE | c.983C>T|p.Thr328Ile |
S229 |
10 | BAA08g22140 | A08 | 16717900 | G | A | missense_variant | MODERATE | c.302C>T|p.Ala101Val |
S37 |
11 | BAA08g22140 | A08 | 16718524 | A | G | missense_variant | MODERATE | c.11T>C|p.Val4Ala |
S245 |
12 | BAA08g22140 | A08 | 16721234 | C | T | upstream_gene_variant | MODIFIER | c.-2700G>A| |
S278 |
13 | BAA08g22140 | A08 | 16722530 | C | T | upstream_gene_variant | MODIFIER | c.-3996G>A| |
S216 |
14 | BAA08g22140 | A08 | 16723319 | G | A | upstream_gene_variant | MODIFIER | c.-4785C>T| |
S55 |