Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19170 | A06 | 9860723 | G | A | upstream_gene_variant | MODIFIER | c.-4548G>A| |
S82 S92 |
2 | BAA06g19170 | A06 | 9863531 | C | T | upstream_gene_variant | MODIFIER | c.-1740C>T| |
S221 |
3 | BAA06g19170 | A06 | 9864648 | G | A | upstream_gene_variant | MODIFIER | c.-623G>A| |
S240 S294 |
4 | BAA06g19170 | A06 | 9866082 | C | T | intron_variant | MODIFIER | c.157+534C>T| |
S99 |
5 | BAA06g19170 | A06 | 9869354 | G | A | intron_variant | MODIFIER | c.158-3341G>A| |
S88 |
6 | BAA06g19170 | A06 | 9869721 | C | T | intron_variant | MODIFIER | c.158-2974C>T| |
S257 |
7 | BAA06g19170 | A06 | 9870057 | G | T | intron_variant | MODIFIER | c.158-2638G>T| |
S19 |
8 | BAA06g19170 | A06 | 9872065 | C | T | intron_variant | MODIFIER | c.158-630C>T| |
S113 S36 |
9 | BAA06g19170 | A06 | 9872702 | G | A | synonymous_variant | LOW | c.165G>A|p.Glu55Glu |
S119 |
10 | BAA06g19170 | A06 | 9872790 | C | T | intron_variant | MODIFIER | c.210+43C>T| |
S55 |
11 | BAA06g19170 | A06 | 9873181 | G | A | intron_variant | MODIFIER | c.280+118G>A| |
S190 |
12 | BAA06g19170 | A06 | 9873830 | G | A | intron_variant | MODIFIER | c.280+767G>A| |
S81 S85 |
13 | BAA06g19170 | A06 | 9874146 | G | A | intron_variant | MODIFIER | c.280+1083G>A| |
S149 |
14 | BAA06g19170 | A06 | 9874193 | G | A | intron_variant | MODIFIER | c.280+1130G>A| |
S85 |
15 | BAA06g19170 | A06 | 9874398 | G | A | intron_variant | MODIFIER | c.280+1335G>A| |
S240 |
16 | BAA06g19170 | A06 | 9875487 | C | T | intron_variant | MODIFIER | c.280+2424C>T| |
S34 |
17 | BAA06g19170 | A06 | 9881077 | G | A | missense_variant | MODERATE | c.524G>A|p.Arg175His |
S100 |
18 | BAA06g19170 | A06 | 9882652 | C | T | missense_variant | MODERATE | c.890C>T|p.Pro297Leu |
S77 |
19 | BAA06g19170 | A06 | 9883717 | G | A | synonymous_variant | LOW | c.1713G>A|p.Leu571Leu |
S54 |
20 | BAA06g19170 | A06 | 9885564 | G | A | synonymous_variant | LOW | c.1827G>A|p.Glu609Glu |
S169 |
21 | BAA06g19170 | A06 | 9885736 | G | A | missense_variant | MODERATE | c.1928G>A|p.Arg643Gln |
S59 |
22 | BAA06g19170 | A06 | 9885962 | G | A | stop_gained | HIGH | c.2154G>A|p.Trp718* |
S292 |