Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g08100 | A06 | 4204026 | C | T | missense_variant | MODERATE | c.3146G>A|p.Arg1049Lys |
S171 |
2 | BAA06g08100 | A06 | 4204424 | C | T | synonymous_variant | LOW | c.2847G>A|p.Lys949Lys |
S178 |
3 | BAA06g08100 | A06 | 4207137 | C | T | synonymous_variant | LOW | c.1494G>A|p.Gln498Gln |
S295 |
4 | BAA06g08100 | A06 | 4207957 | C | T | stop_gained | HIGH | c.845G>A|p.Trp282* |
S308 S94 |
5 | BAA06g08100 | A06 | 4208117 | C | T | missense_variant&splice_region_variant | MODERATE | c.685G>A|p.Val229Met |
S84 S93 |
6 | BAA06g08100 | A06 | 4208714 | A | T | missense_variant | MODERATE | c.392T>A|p.Ile131Lys |
S5 |
7 | BAA06g08100 | A06 | 4208739 | G | A | missense_variant | MODERATE | c.367C>T|p.Leu123Phe |
S295 |
8 | BAA06g08100 | A06 | 4210689 | C | T | upstream_gene_variant | MODIFIER | c.-192G>A| |
S96 |
9 | BAA06g08100 | A06 | 4211177 | C | T | upstream_gene_variant | MODIFIER | c.-680G>A| |
S60 |
10 | BAA06g08100 | A06 | 4212100 | G | A | upstream_gene_variant | MODIFIER | c.-1603C>T| |
S297 |
11 | BAA06g08100 | A06 | 4213220 | G | A | upstream_gene_variant | MODIFIER | c.-2723C>T| |
S161 |
12 | BAA06g08100 | A06 | 4213383 | C | T | upstream_gene_variant | MODIFIER | c.-2886G>A| |
S277 |
13 | BAA06g08100 | A06 | 4213390 | C | T | upstream_gene_variant | MODIFIER | c.-2893G>A| |
S270 |
14 | BAA06g08100 | A06 | 4213509 | C | T | upstream_gene_variant | MODIFIER | c.-3012G>A| |
S183 S198 |
15 | BAA06g08100 | A06 | 4213694 | G | A | upstream_gene_variant | MODIFIER | c.-3197C>T| |
S138 |
16 | BAA06g08100 | A06 | 4215480 | C | T | upstream_gene_variant | MODIFIER | c.-4983G>A| |
S237 |