Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10300 | A01 | 4705314 | G | A | missense_variant | MODERATE | c.20C>T|p.Pro7Leu |
S229 |
2 | BAA01g10300 | A01 | 4705702 | G | A | upstream_gene_variant | MODIFIER | c.-369C>T| |
S245 |
3 | BAA01g10300 | A01 | 4707107 | G | A | upstream_gene_variant | MODIFIER | c.-1774C>T| |
S297 |
4 | BAA01g10300 | A01 | 4708130 | C | T | upstream_gene_variant | MODIFIER | c.-2797G>A| |
S109 |
5 | BAA01g10300 | A01 | 4708807 | C | T | upstream_gene_variant | MODIFIER | c.-3474G>A| |
S81 S85 |
6 | BAA01g10300 | A01 | 4709223 | G | A | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S306 S308 |
7 | BAA01g10300 | A01 | 4709429 | C | T | upstream_gene_variant | MODIFIER | c.-4096G>A| |
S44 |
8 | BAA01g10300 | A01 | 4709538 | C | T | upstream_gene_variant | MODIFIER | c.-4205G>A| |
S203 |
9 | BAA01g10300 | A01 | 4709603 | G | A | upstream_gene_variant | MODIFIER | c.-4270C>T| |
S256 |
10 | BAA01g10300 | A01 | 4709869 | G | A | upstream_gene_variant | MODIFIER | c.-4536C>T| |
S85 |