Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11850 | A04 | 17767321 | T | C | upstream_gene_variant | MODIFIER | c.-4996T>C| |
S114 |
2 | BAA04g11850 | A04 | 17768310 | C | T | upstream_gene_variant | MODIFIER | c.-4007C>T| |
S297 |
3 | BAA04g11850 | A04 | 17768485 | G | A | upstream_gene_variant | MODIFIER | c.-3832G>A| |
S62 |
4 | BAA04g11850 | A04 | 17768791 | G | A | upstream_gene_variant | MODIFIER | c.-3526G>A| |
|
5 | BAA04g11850 | A04 | 17769250 | G | A | upstream_gene_variant | MODIFIER | c.-3067G>A| |
S15 S3 |
6 | BAA04g11850 | A04 | 17770402 | G | A | upstream_gene_variant | MODIFIER | c.-1915G>A| |
S43 |
7 | BAA04g11850 | A04 | 17770657 | G | A | upstream_gene_variant | MODIFIER | c.-1660G>A| |
S127 |
8 | BAA04g11850 | A04 | 17770680 | C | A | upstream_gene_variant | MODIFIER | c.-1637C>A| |
S202 |
9 | BAA04g11850 | A04 | 17772141 | C | T | upstream_gene_variant | MODIFIER | c.-176C>T| |
S209 |
10 | BAA04g11850 | A04 | 17772286 | G | A | upstream_gene_variant | MODIFIER | c.-31G>A| |
S43 |
11 | BAA04g11850 | A04 | 17773167 | G | A | missense_variant | MODERATE | c.562G>A|p.Val188Met |
S47 |
12 | BAA04g11850 | A04 | 17774024 | G | A | intron_variant | MODIFIER | c.952-58G>A| |
S155 S211 |
13 | BAA04g11850 | A04 | 17774701 | C | T | missense_variant | MODERATE | c.1235C>T|p.Ala412Val |
S179 |
14 | BAA04g11850 | A04 | 17775006 | G | A | intron_variant | MODIFIER | c.1324-79G>A| |
S170 |
15 | BAA04g11850 | A04 | 17775741 | G | A | intron_variant | MODIFIER | c.1555+51G>A| |
S169 |