Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29330 | A10 | 22113841 | C | T | missense_variant | MODERATE | c.1732G>A|p.Gly578Ser |
S218 |
2 | BAA10g29330 | A10 | 22114146 | C | T | stop_gained | HIGH | c.1551G>A|p.Trp517* |
S44 |
3 | BAA10g29330 | A10 | 22114904 | G | A | synonymous_variant | LOW | c.1065C>T|p.Phe355Phe |
S179 |
4 | BAA10g29330 | A10 | 22115154 | C | T | synonymous_variant | LOW | c.897G>A|p.Gln299Gln |
S306 S308 |
5 | BAA10g29330 | A10 | 22115183 | C | T | missense_variant | MODERATE | c.868G>A|p.Val290Ile |
S204 |
6 | BAA10g29330 | A10 | 22116019 | C | A | stop_gained | HIGH | c.460G>T|p.Glu154* |
S11 |
7 | BAA10g29330 | A10 | 22116553 | C | T | missense_variant | MODERATE | c.79G>A|p.Gly27Ser |
S161 |
8 | BAA10g29330 | A10 | 22116777 | T | G | upstream_gene_variant | MODIFIER | c.-146A>C| |
S143 |
9 | BAA10g29330 | A10 | 22118342 | G | A | upstream_gene_variant | MODIFIER | c.-1711C>T| |
S180 |
10 | BAA10g29330 | A10 | 22118771 | G | A | upstream_gene_variant | MODIFIER | c.-2140C>T| |
S94 |
11 | BAA10g29330 | A10 | 22119943 | G | A | upstream_gene_variant | MODIFIER | c.-3312C>T| |
S4 |