Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g25740 | A10 | 20669485 | C | T | missense_variant | MODERATE | c.1467G>A|p.Met489Ile |
S37 |
2 | BAA10g25740 | A10 | 20669941 | G | A | missense_variant | MODERATE | c.1181C>T|p.Pro394Leu |
S32 |
3 | BAA10g25740 | A10 | 20670860 | G | A | splice_region_variant&intron_variant | LOW | c.702+8C>T| |
S57 |
4 | BAA10g25740 | A10 | 20674096 | G | A | upstream_gene_variant | MODIFIER | c.-2219C>T| |
S173 |
5 | BAA10g25740 | A10 | 20675910 | G | A | upstream_gene_variant | MODIFIER | c.-4033C>T| |
S257 |
6 | BAA10g25740 | A10 | 20676131 | C | T | upstream_gene_variant | MODIFIER | c.-4254G>A| |
S161 |
7 | BAA10g25740 | A10 | 20676678 | C | T | upstream_gene_variant | MODIFIER | c.-4801G>A| |
S188 |
8 | BAA10g25740 | A10 | 20676779 | G | A | upstream_gene_variant | MODIFIER | c.-4902C>T| |
S271 |