Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17220 | A09 | 10258495 | C | T | upstream_gene_variant | MODIFIER | c.-4859C>T| |
S125 |
2 | BAA09g17220 | A09 | 10258499 | G | A | upstream_gene_variant | MODIFIER | c.-4855G>A| |
S122 |
3 | BAA09g17220 | A09 | 10258531 | G | A | upstream_gene_variant | MODIFIER | c.-4823G>A| |
S199 |
4 | BAA09g17220 | A09 | 10258602 | C | T | upstream_gene_variant | MODIFIER | c.-4752C>T| |
S50 |
5 | BAA09g17220 | A09 | 10259021 | G | A | upstream_gene_variant | MODIFIER | c.-4333G>A| |
S193 |
6 | BAA09g17220 | A09 | 10259669 | C | T | upstream_gene_variant | MODIFIER | c.-3685C>T| |
S120 |
7 | BAA09g17220 | A09 | 10259900 | G | A | upstream_gene_variant | MODIFIER | c.-3454G>A| |
S91 |
8 | BAA09g17220 | A09 | 10259932 | C | T | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S296 |
9 | BAA09g17220 | A09 | 10260459 | C | T | upstream_gene_variant | MODIFIER | c.-2895C>T| |
S168 |
10 | BAA09g17220 | A09 | 10260813 | G | A | upstream_gene_variant | MODIFIER | c.-2541G>A| |
S208 S219 |
11 | BAA09g17220 | A09 | 10261420 | C | T | upstream_gene_variant | MODIFIER | c.-1934C>T| |
S255 |
12 | BAA09g17220 | A09 | 10262290 | C | T | upstream_gene_variant | MODIFIER | c.-1064C>T| |
S36 |
13 | BAA09g17220 | A09 | 10263890 | C | T | synonymous_variant | LOW | c.417C>T|p.Phe139Phe |
S85 |
14 | BAA09g17220 | A09 | 10264443 | C | T | missense_variant | MODERATE | c.785C>T|p.Thr262Ile |
S143 |
15 | BAA09g17220 | A09 | 10265893 | C | T | downstream_gene_variant | MODIFIER | c.*447C>T| |
S272 |
16 | BAA09g17220 | A09 | 10267617 | G | A | downstream_gene_variant | MODIFIER | c.*2171G>A| |
S129 |
17 | BAA09g17220 | A09 | 10269323 | C | T | downstream_gene_variant | MODIFIER | c.*3877C>T| |
S111 |
18 | BAA09g17220 | A09 | 10269679 | G | A | downstream_gene_variant | MODIFIER | c.*4233G>A| |
S151 |