Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08480 | A05 | 4224939 | G | A | missense_variant | MODERATE | c.1688C>T|p.Ser563Phe |
S298 |
2 | BAA05g08480 | A05 | 4225337 | G | A | splice_region_variant&intron_variant | LOW | c.1482+8C>T| |
S56 |
3 | BAA05g08480 | A05 | 4225527 | G | A | missense_variant | MODERATE | c.1391C>T|p.Thr464Ile |
S13 |
4 | BAA05g08480 | A05 | 4225648 | G | A | intron_variant | MODIFIER | c.1349+20C>T| |
S192 |
5 | BAA05g08480 | A05 | 4226722 | C | T | synonymous_variant | LOW | c.879G>A|p.Leu293Leu |
S33 |
6 | BAA05g08480 | A05 | 4226815 | C | T | missense_variant | MODERATE | c.859G>A|p.Glu287Lys |
S99 |
7 | BAA05g08480 | A05 | 4226839 | C | T | missense_variant | MODERATE | c.835G>A|p.Glu279Lys |
S174 S27 |
8 | BAA05g08480 | A05 | 4227477 | C | T | missense_variant | MODERATE | c.799G>A|p.Gly267Arg |
S143 |
9 | BAA05g08480 | A05 | 4230053 | C | T | missense_variant | MODERATE | c.139G>A|p.Ala47Thr |
S19 |
10 | BAA05g08480 | A05 | 4231705 | G | A | upstream_gene_variant | MODIFIER | c.-1021C>T| |
S187 S188 S276 S298 |
11 | BAA05g08480 | A05 | 4232176 | C | T | upstream_gene_variant | MODIFIER | c.-1492G>A| |
S2 |
12 | BAA05g08480 | A05 | 4232196 | G | A | upstream_gene_variant | MODIFIER | c.-1512C>T| |
S190 |
13 | BAA05g08480 | A05 | 4233997 | G | A | upstream_gene_variant | MODIFIER | c.-3313C>T| |
S187 |
14 | BAA05g08480 | A05 | 4234222 | C | T | upstream_gene_variant | MODIFIER | c.-3538G>A| |
S69 |