Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g15960 | A06 | 7904025 | G | A | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S177 |
2 | BAA06g15960 | A06 | 7905520 | G | A | upstream_gene_variant | MODIFIER | c.-3289G>A| |
S292 |
3 | BAA06g15960 | A06 | 7905678 | G | A | upstream_gene_variant | MODIFIER | c.-3131G>A| |
S119 |
4 | BAA06g15960 | A06 | 7906420 | G | A | upstream_gene_variant | MODIFIER | c.-2389G>A| |
S275 |
5 | BAA06g15960 | A06 | 7906551 | G | A | upstream_gene_variant | MODIFIER | c.-2258G>A| |
S13 |
6 | BAA06g15960 | A06 | 7906841 | C | T | upstream_gene_variant | MODIFIER | c.-1968C>T| |
S62 |
7 | BAA06g15960 | A06 | 7908593 | G | A | upstream_gene_variant | MODIFIER | c.-216G>A| |
S64 |
8 | BAA06g15960 | A06 | 7909349 | C | T | synonymous_variant | LOW | c.378C>T|p.Asp126Asp |
S162 |
9 | BAA06g15960 | A06 | 7909411 | G | A | missense_variant | MODERATE | c.440G>A|p.Gly147Glu |
S53 |
10 | BAA06g15960 | A06 | 7909601 | G | A | synonymous_variant | LOW | c.630G>A|p.Arg210Arg |
S274 |