Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g03490 | A07 | 2795426 | G | A | missense_variant | MODERATE | c.112G>A|p.Glu38Lys |
S255 |
2 | BAA07g03490 | A07 | 2796005 | C | T | intron_variant | MODIFIER | c.367-99C>T| |
S162 |
3 | BAA07g03490 | A07 | 2796149 | G | A | downstream_gene_variant | MODIFIER | c.*31G>A| |
S201 |
4 | BAA07g03490 | A07 | 2796918 | C | T | downstream_gene_variant | MODIFIER | c.*800C>T| |
S161 |
5 | BAA07g03490 | A07 | 2797046 | C | T | downstream_gene_variant | MODIFIER | c.*928C>T| |
S90 |
6 | BAA07g03490 | A07 | 2797172 | C | T | downstream_gene_variant | MODIFIER | c.*1054C>T| |
S35 |
7 | BAA07g03490 | A07 | 2798699 | C | T | downstream_gene_variant | MODIFIER | c.*2581C>T| |
S130 |
8 | BAA07g03490 | A07 | 2799966 | G | A | downstream_gene_variant | MODIFIER | c.*3848G>A| |
S219 |
9 | BAA07g03490 | A07 | 2800313 | C | T | downstream_gene_variant | MODIFIER | c.*4195C>T| |
S133 |
10 | BAA07g03490 | A07 | 2800335 | G | A | downstream_gene_variant | MODIFIER | c.*4217G>A| |
S25 |
11 | BAA07g03490 | A07 | 2800883 | C | T | downstream_gene_variant | MODIFIER | c.*4765C>T| |
S136 |
12 | BAA07g03490 | A07 | 2801018 | G | A | downstream_gene_variant | MODIFIER | c.*4900G>A| |
S202 |