Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g29530 | A09 | 19762737 | C | T | downstream_gene_variant | MODIFIER | c.*435G>A| |
S208 S219 |
2 | BAA09g29530 | A09 | 19763002 | G | A | downstream_gene_variant | MODIFIER | c.*170C>T| |
S162 |
3 | BAA09g29530 | A09 | 19763532 | G | A | synonymous_variant | LOW | c.3099C>T|p.Pro1033Pro |
S88 |
4 | BAA09g29530 | A09 | 19763645 | G | A | missense_variant | MODERATE | c.2986C>T|p.Pro996Ser |
S25 |
5 | BAA09g29530 | A09 | 19763726 | C | T | missense_variant | MODERATE | c.2905G>A|p.Ala969Thr |
S297 |
6 | BAA09g29530 | A09 | 19764172 | C | T | missense_variant | MODERATE | c.2459G>A|p.Arg820Gln |
S289 S290 |
7 | BAA09g29530 | A09 | 19764208 | C | T | missense_variant | MODERATE | c.2423G>A|p.Gly808Asp |
S293 |
8 | BAA09g29530 | A09 | 19764230 | C | T | missense_variant | MODERATE | c.2401G>A|p.Ala801Thr |
S293 |
9 | BAA09g29530 | A09 | 19764475 | C | T | missense_variant | MODERATE | c.2336G>A|p.Cys779Tyr |
S263 |
10 | BAA09g29530 | A09 | 19764596 | G | A | missense_variant | MODERATE | c.2215C>T|p.Pro739Ser |
S266 |
11 | BAA09g29530 | A09 | 19764625 | C | T | missense_variant | MODERATE | c.2186G>A|p.Gly729Glu |
S231 |
12 | BAA09g29530 | A09 | 19764812 | C | T | missense_variant | MODERATE | c.2074G>A|p.Glu692Lys |
S95 |
13 | BAA09g29530 | A09 | 19765299 | C | T | intron_variant | MODIFIER | c.1616-29G>A| |
S4 |
14 | BAA09g29530 | A09 | 19765977 | G | T | intron_variant | MODIFIER | c.1616-707C>A| |
S274 |
15 | BAA09g29530 | A09 | 19766121 | C | T | intron_variant | MODIFIER | c.1616-851G>A| |
S174 S27 |
16 | BAA09g29530 | A09 | 19766640 | C | T | intron_variant | MODIFIER | c.1615+1128G>A| |
S234 |
17 | BAA09g29530 | A09 | 19767938 | G | A | intron_variant | MODIFIER | c.1477-32C>T| |
S229 |
18 | BAA09g29530 | A09 | 19768458 | G | A | missense_variant | MODERATE | c.1166C>T|p.Ser389Leu |
S185 |
19 | BAA09g29530 | A09 | 19769798 | C | T | intron_variant | MODIFIER | c.816+178G>A| |
S274 S294 |
20 | BAA09g29530 | A09 | 19769953 | G | A | intron_variant | MODIFIER | c.816+23C>T| |
S221 |
21 | BAA09g29530 | A09 | 19770048 | G | A | synonymous_variant | LOW | c.744C>T|p.Arg248Arg |
S129 |
22 | BAA09g29530 | A09 | 19770126 | G | A | intron_variant | MODIFIER | c.728+18C>T| |
S185 |
23 | BAA09g29530 | A09 | 19770165 | C | T | missense_variant | MODERATE | c.707G>A|p.Gly236Glu |
S277 |
24 | BAA09g29530 | A09 | 19770531 | G | A | intron_variant | MODIFIER | c.597+136C>T| |
S251 |
25 | BAA09g29530 | A09 | 19770542 | G | A | intron_variant | MODIFIER | c.597+125C>T| |
S53 |