Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00250 | A01 | 119762 | C | T | missense_variant | MODERATE | c.2024G>A|p.Gly675Glu |
S219 S72 |
2 | BAA01g00250 | A01 | 120696 | G | T | missense_variant | MODERATE | c.1246C>A|p.Leu416Ile |
S292 |
3 | BAA01g00250 | A01 | 120840 | G | A | splice_region_variant&intron_variant | LOW | c.1164+8C>T| |
S200 |
4 | BAA01g00250 | A01 | 122097 | C | T | missense_variant | MODERATE | c.385G>A|p.Ala129Thr |
S305 |
5 | BAA01g00250 | A01 | 124268 | G | A | upstream_gene_variant | MODIFIER | c.-1305C>T| |
S292 |
6 | BAA01g00250 | A01 | 126504 | C | T | upstream_gene_variant | MODIFIER | c.-3541G>A| |
S80 |
7 | BAA01g00250 | A01 | 126783 | G | A | upstream_gene_variant | MODIFIER | c.-3820C>T| |
S251 |
8 | BAA01g00250 | A01 | 127603 | C | T | upstream_gene_variant | MODIFIER | c.-4640G>A| |
S66 |
9 | BAA01g00250 | A01 | 127721 | C | T | upstream_gene_variant | MODIFIER | c.-4758G>A| |
S62 |