Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g07880 | A09 | 4401009 | G | A | downstream_gene_variant | MODIFIER | c.*4957C>T| |
S126 |
2 | BAA09g07880 | A09 | 4401106 | G | A | downstream_gene_variant | MODIFIER | c.*4860C>T| |
S67 |
3 | BAA09g07880 | A09 | 4401875 | G | A | downstream_gene_variant | MODIFIER | c.*4091C>T| |
S218 |
4 | BAA09g07880 | A09 | 4402387 | G | A | downstream_gene_variant | MODIFIER | c.*3579C>T| |
S308 |
5 | BAA09g07880 | A09 | 4404645 | G | A | downstream_gene_variant | MODIFIER | c.*1321C>T| |
S167 |
6 | BAA09g07880 | A09 | 4406183 | C | T | splice_region_variant&intron_variant | LOW | c.717+8G>A| |
S208 S219 |
7 | BAA09g07880 | A09 | 4406790 | C | T | missense_variant | MODERATE | c.352G>A|p.Gly118Arg |
S250 |
8 | BAA09g07880 | A09 | 4411377 | G | A | upstream_gene_variant | MODIFIER | c.-3587C>T| |
S182 |
9 | BAA09g07880 | A09 | 4411773 | G | A | upstream_gene_variant | MODIFIER | c.-3983C>T| |
S180 |
10 | BAA09g07880 | A09 | 4411998 | G | A | upstream_gene_variant | MODIFIER | c.-4208C>T| |
S185 |