Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12600 | A08 | 11039794 | G | A | downstream_gene_variant | MODIFIER | c.*4302C>T| |
S286 |
2 | BAA08g12600 | A08 | 11039975 | G | A | downstream_gene_variant | MODIFIER | c.*4121C>T| |
S133 |
3 | BAA08g12600 | A08 | 11040218 | G | A | downstream_gene_variant | MODIFIER | c.*3878C>T| |
S11 |
4 | BAA08g12600 | A08 | 11040460 | C | T | downstream_gene_variant | MODIFIER | c.*3636G>A| |
S175 |
5 | BAA08g12600 | A08 | 11040594 | G | T | downstream_gene_variant | MODIFIER | c.*3502C>A| |
S201 |
6 | BAA08g12600 | A08 | 11040674 | C | T | downstream_gene_variant | MODIFIER | c.*3422G>A| |
S219 |
7 | BAA08g12600 | A08 | 11041086 | G | A | downstream_gene_variant | MODIFIER | c.*3010C>T| |
S202 |
8 | BAA08g12600 | A08 | 11041132 | C | T | downstream_gene_variant | MODIFIER | c.*2964G>A| |
S305 |
9 | BAA08g12600 | A08 | 11041400 | C | T | downstream_gene_variant | MODIFIER | c.*2696G>A| |
S46 |
10 | BAA08g12600 | A08 | 11042456 | G | A | downstream_gene_variant | MODIFIER | c.*1640C>T| |
S260 |
11 | BAA08g12600 | A08 | 11042556 | G | A | downstream_gene_variant | MODIFIER | c.*1540C>T| |
S68 |
12 | BAA08g12600 | A08 | 11044572 | C | T | missense_variant | MODERATE | c.541G>A|p.Gly181Arg |
S144 |
13 | BAA08g12600 | A08 | 11044742 | C | T | missense_variant | MODERATE | c.493G>A|p.Asp165Asn |
S167 |
14 | BAA08g12600 | A08 | 11045237 | C | T | upstream_gene_variant | MODIFIER | c.-3G>A| |
S46 |
15 | BAA08g12600 | A08 | 11047012 | C | T | upstream_gene_variant | MODIFIER | c.-1778G>A| |
S289 S290 |
16 | BAA08g12600 | A08 | 11047037 | C | T | upstream_gene_variant | MODIFIER | c.-1803G>A| |
S230 |
17 | BAA08g12600 | A08 | 11047797 | G | A | upstream_gene_variant | MODIFIER | c.-2563C>T| |
S192 |
18 | BAA08g12600 | A08 | 11048685 | G | A | upstream_gene_variant | MODIFIER | c.-3451C>T| |
S218 |