Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22730 | A08 | 16988765 | G | A | upstream_gene_variant | MODIFIER | c.-4587G>A| |
S100 |
2 | BAA08g22730 | A08 | 16988789 | G | A | upstream_gene_variant | MODIFIER | c.-4563G>A| |
S219 |
3 | BAA08g22730 | A08 | 16989162 | G | A | upstream_gene_variant | MODIFIER | c.-4190G>A| |
S188 |
4 | BAA08g22730 | A08 | 16989474 | G | A | upstream_gene_variant | MODIFIER | c.-3878G>A| |
S188 |
5 | BAA08g22730 | A08 | 16990523 | C | T | upstream_gene_variant | MODIFIER | c.-2829C>T| |
S261 |
6 | BAA08g22730 | A08 | 16990596 | C | A | upstream_gene_variant | MODIFIER | c.-2756C>A| |
S113 S115 S117 S121 S122 S23 S266 S297 S55 S8 S9 |
7 | BAA08g22730 | A08 | 16991304 | C | T | upstream_gene_variant | MODIFIER | c.-2048C>T| |
S293 |
8 | BAA08g22730 | A08 | 16991351 | C | T | upstream_gene_variant | MODIFIER | c.-2001C>T| |
S157 S163 |
9 | BAA08g22730 | A08 | 16991758 | C | T | upstream_gene_variant | MODIFIER | c.-1594C>T| |
S284 |
10 | BAA08g22730 | A08 | 16991795 | C | T | upstream_gene_variant | MODIFIER | c.-1557C>T| |
S73 |
11 | BAA08g22730 | A08 | 16992094 | G | A | upstream_gene_variant | MODIFIER | c.-1258G>A| |
S162 |
12 | BAA08g22730 | A08 | 16993396 | C | T | synonymous_variant | LOW | c.45C>T|p.Cys15Cys |
S82 S92 |
13 | BAA08g22730 | A08 | 16994058 | G | A | missense_variant | MODERATE | c.707G>A|p.Arg236Gln |
S221 |
14 | BAA08g22730 | A08 | 16994337 | C | T | missense_variant | MODERATE | c.986C>T|p.Thr329Ile |
S172 |
15 | BAA08g22730 | A08 | 16995477 | G | A | downstream_gene_variant | MODIFIER | c.*551G>A| |
S97 |
16 | BAA08g22730 | A08 | 16996846 | C | T | downstream_gene_variant | MODIFIER | c.*1920C>T| |
S288 |
17 | BAA08g22730 | A08 | 16996886 | C | T | downstream_gene_variant | MODIFIER | c.*1960C>T| |
S50 |
18 | BAA08g22730 | A08 | 16997636 | G | A | downstream_gene_variant | MODIFIER | c.*2710G>A| |
S291 |
19 | BAA08g22730 | A08 | 16998228 | C | T | downstream_gene_variant | MODIFIER | c.*3302C>T| |
S169 |