Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20440 | A09 | 12634717 | G | A | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S128 |
2 | BAA09g20440 | A09 | 12635653 | G | A | upstream_gene_variant | MODIFIER | c.-3085G>A| |
S59 |
3 | BAA09g20440 | A09 | 12635868 | G | A | upstream_gene_variant | MODIFIER | c.-2870G>A| |
S170 |
4 | BAA09g20440 | A09 | 12635935 | C | T | upstream_gene_variant | MODIFIER | c.-2803C>T| |
S217 |
5 | BAA09g20440 | A09 | 12636379 | G | A | upstream_gene_variant | MODIFIER | c.-2359G>A| |
S34 |
6 | BAA09g20440 | A09 | 12636428 | C | T | upstream_gene_variant | MODIFIER | c.-2310C>T| |
S67 |
7 | BAA09g20440 | A09 | 12636591 | C | T | upstream_gene_variant | MODIFIER | c.-2147C>T| |
S296 |
8 | BAA09g20440 | A09 | 12637063 | C | T | upstream_gene_variant | MODIFIER | c.-1675C>T| |
S289 S290 |
9 | BAA09g20440 | A09 | 12637581 | C | A | upstream_gene_variant | MODIFIER | c.-1157C>A| |
S66 |
10 | BAA09g20440 | A09 | 12638004 | G | A | upstream_gene_variant | MODIFIER | c.-734G>A| |
S80 |
11 | BAA09g20440 | A09 | 12639688 | G | A | missense_variant | MODERATE | c.647G>A|p.Gly216Glu |
S280 |
12 | BAA09g20440 | A09 | 12641015 | G | A | downstream_gene_variant | MODIFIER | c.*1161G>A| |
S142 |
13 | BAA09g20440 | A09 | 12644028 | C | T | downstream_gene_variant | MODIFIER | c.*4174C>T| |
S289 S290 |
14 | BAA09g20440 | A09 | 12644036 | C | T | downstream_gene_variant | MODIFIER | c.*4182C>T| |
S119 |
15 | BAA09g20440 | A09 | 12644084 | G | A | downstream_gene_variant | MODIFIER | c.*4230G>A| |
S150 |