Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03620 | A10 | 1739902 | G | A | stop_gained | HIGH | c.36G>A|p.Trp12* |
S306 S308 |
2 | BAA10g03620 | A10 | 1740078 | G | A | missense_variant | MODERATE | c.212G>A|p.Arg71Lys |
S180 |
3 | BAA10g03620 | A10 | 1740185 | G | A | missense_variant | MODERATE | c.319G>A|p.Glu107Lys |
S72 S78 |
4 | BAA10g03620 | A10 | 1740287 | G | A | missense_variant | MODERATE | c.421G>A|p.Glu141Lys |
S13 |
5 | BAA10g03620 | A10 | 1740772 | G | A | downstream_gene_variant | MODIFIER | c.*10G>A| |
S263 |
6 | BAA10g03620 | A10 | 1741156 | G | A | downstream_gene_variant | MODIFIER | c.*394G>A| |
S78 |
7 | BAA10g03620 | A10 | 1742114 | C | T | downstream_gene_variant | MODIFIER | c.*1352C>T| |
S144 |
8 | BAA10g03620 | A10 | 1742115 | C | T | downstream_gene_variant | MODIFIER | c.*1353C>T| |
S110 |
9 | BAA10g03620 | A10 | 1742899 | G | A | downstream_gene_variant | MODIFIER | c.*2137G>A| |
S257 |
10 | BAA10g03620 | A10 | 1744136 | G | A | downstream_gene_variant | MODIFIER | c.*3374G>A| |
S55 |
11 | BAA10g03620 | A10 | 1744227 | G | A | downstream_gene_variant | MODIFIER | c.*3465G>A| |
S289 |
12 | BAA10g03620 | A10 | 1744329 | G | A | downstream_gene_variant | MODIFIER | c.*3567G>A| |
S219 |
13 | BAA10g03620 | A10 | 1744664 | G | A | downstream_gene_variant | MODIFIER | c.*3902G>A| |
S293 |
14 | BAA10g03620 | A10 | 1744718 | G | T | downstream_gene_variant | MODIFIER | c.*3956G>T| |
S64 |
15 | BAA10g03620 | A10 | 1745204 | G | T | downstream_gene_variant | MODIFIER | c.*4442G>T| |
S163 |
16 | BAA10g03620 | A10 | 1745685 | G | A | downstream_gene_variant | MODIFIER | c.*4923G>A| |
S38 |