Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16820 | A05 | 9389154 | G | A | upstream_gene_variant | MODIFIER | c.-4414G>A| |
S266 |
2 | BAA05g16820 | A05 | 9389589 | C | A | upstream_gene_variant | MODIFIER | c.-3979C>A| |
S106 |
3 | BAA05g16820 | A05 | 9389708 | G | A | upstream_gene_variant | MODIFIER | c.-3860G>A| |
S86 |
4 | BAA05g16820 | A05 | 9390087 | G | A | upstream_gene_variant | MODIFIER | c.-3481G>A| |
S47 |
5 | BAA05g16820 | A05 | 9390465 | C | T | upstream_gene_variant | MODIFIER | c.-3103C>T| |
S87 |
6 | BAA05g16820 | A05 | 9392438 | C | T | upstream_gene_variant | MODIFIER | c.-1130C>T| |
S107 |
7 | BAA05g16820 | A05 | 9392813 | C | T | upstream_gene_variant | MODIFIER | c.-755C>T| |
S5 |
8 | BAA05g16820 | A05 | 9393783 | C | T | missense_variant | MODERATE | c.131C>T|p.Ser44Phe |
S67 |
9 | BAA05g16820 | A05 | 9394159 | C | T | missense_variant | MODERATE | c.424C>T|p.Pro142Ser |
S249 |
10 | BAA05g16820 | A05 | 9395409 | G | A | downstream_gene_variant | MODIFIER | c.*650G>A| |
S144 |
11 | BAA05g16820 | A05 | 9397080 | G | A | downstream_gene_variant | MODIFIER | c.*2321G>A| |
S208 S219 |
12 | BAA05g16820 | A05 | 9397124 | C | T | downstream_gene_variant | MODIFIER | c.*2365C>T| |
S262 |
13 | BAA05g16820 | A05 | 9397307 | C | T | downstream_gene_variant | MODIFIER | c.*2548C>T| |
S87 |
14 | BAA05g16820 | A05 | 9397555 | G | A | downstream_gene_variant | MODIFIER | c.*2796G>A| |
S197 |
15 | BAA05g16820 | A05 | 9397864 | G | A | downstream_gene_variant | MODIFIER | c.*3105G>A| |
S107 |
16 | BAA05g16820 | A05 | 9398227 | C | T | downstream_gene_variant | MODIFIER | c.*3468C>T| |
S184 |
17 | BAA05g16820 | A05 | 9399091 | C | T | downstream_gene_variant | MODIFIER | c.*4332C>T| |
S13 |
18 | BAA05g16820 | A05 | 9399506 | C | T | downstream_gene_variant | MODIFIER | c.*4747C>T| |
S228 |