Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03460 | A10 | 1681764 | C | T | missense_variant | MODERATE | c.455G>A|p.Gly152Glu |
S210 |
2 | BAA10g03460 | A10 | 1681905 | C | T | missense_variant | MODERATE | c.314G>A|p.Arg105Lys |
S270 |
3 | BAA10g03460 | A10 | 1683056 | G | A | upstream_gene_variant | MODIFIER | c.-838C>T| |
S50 |
4 | BAA10g03460 | A10 | 1683207 | G | A | upstream_gene_variant | MODIFIER | c.-989C>T| |
S303 |
5 | BAA10g03460 | A10 | 1683885 | C | A | upstream_gene_variant | MODIFIER | c.-1667G>T| |
S31 |
6 | BAA10g03460 | A10 | 1683954 | C | T | upstream_gene_variant | MODIFIER | c.-1736G>A| |
S202 |
7 | BAA10g03460 | A10 | 1685696 | G | A | upstream_gene_variant | MODIFIER | c.-3478C>T| |
S255 |
8 | BAA10g03460 | A10 | 1685709 | G | A | upstream_gene_variant | MODIFIER | c.-3491C>T| |
S38 |
9 | BAA10g03460 | A10 | 1686665 | C | T | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S2 |
10 | BAA10g03460 | A10 | 1686989 | G | A | upstream_gene_variant | MODIFIER | c.-4771C>T| |
S48 |
11 | BAA10g03460 | A10 | 1687106 | C | T | upstream_gene_variant | MODIFIER | c.-4888G>A| |
S173 |