Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19720 | A01 | 9709340 | G | A | upstream_gene_variant | MODIFIER | c.-4898G>A| |
S23 |
2 | BAA01g19720 | A01 | 9709355 | C | T | upstream_gene_variant | MODIFIER | c.-4883C>T| |
S177 |
3 | BAA01g19720 | A01 | 9710125 | C | T | upstream_gene_variant | MODIFIER | c.-4113C>T| |
S4 |
4 | BAA01g19720 | A01 | 9712050 | G | A | upstream_gene_variant | MODIFIER | c.-2188G>A| |
S149 |
5 | BAA01g19720 | A01 | 9712257 | G | A | upstream_gene_variant | MODIFIER | c.-1981G>A| |
S15 S3 |
6 | BAA01g19720 | A01 | 9713498 | C | T | upstream_gene_variant | MODIFIER | c.-740C>T| |
S148 S30 S31 |
7 | BAA01g19720 | A01 | 9713895 | G | A | upstream_gene_variant | MODIFIER | c.-343G>A| |
S298 |
8 | BAA01g19720 | A01 | 9713975 | A | T | upstream_gene_variant | MODIFIER | c.-263A>T| |
S145 S195 S231 S245 S246 S277 S66 |
9 | BAA01g19720 | A01 | 9714659 | C | T | missense_variant | MODERATE | c.422C>T|p.Pro141Leu |
S146 |