Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g09910 | A07 | 18805121 | G | A | upstream_gene_variant | MODIFIER | c.-4999G>A| |
S249 |
2 | BAA07g09910 | A07 | 18805681 | C | T | upstream_gene_variant | MODIFIER | c.-4439C>T| |
S113 |
3 | BAA07g09910 | A07 | 18806411 | C | T | upstream_gene_variant | MODIFIER | c.-3709C>T| |
S247 |
4 | BAA07g09910 | A07 | 18807153 | C | T | upstream_gene_variant | MODIFIER | c.-2967C>T| |
S126 |
5 | BAA07g09910 | A07 | 18807173 | T | A | upstream_gene_variant | MODIFIER | c.-2947T>A| |
S55 |
6 | BAA07g09910 | A07 | 18807932 | G | A | upstream_gene_variant | MODIFIER | c.-2188G>A| |
S240 |
7 | BAA07g09910 | A07 | 18808151 | G | A | upstream_gene_variant | MODIFIER | c.-1969G>A| |
S112 |
8 | BAA07g09910 | A07 | 18809213 | C | T | upstream_gene_variant | MODIFIER | c.-907C>T| |
S146 |
9 | BAA07g09910 | A07 | 18810541 | C | T | missense_variant | MODERATE | c.422C>T|p.Thr141Ile |
S80 |
10 | BAA07g09910 | A07 | 18811322 | C | T | synonymous_variant | LOW | c.1137C>T|p.Leu379Leu |
S9 |
11 | BAA07g09910 | A07 | 18811349 | C | T | synonymous_variant | LOW | c.1164C>T|p.Asn388Asn |
S41 |
12 | BAA07g09910 | A07 | 18811937 | C | T | downstream_gene_variant | MODIFIER | c.*549C>T| |
S42 |
13 | BAA07g09910 | A07 | 18812286 | C | T | downstream_gene_variant | MODIFIER | c.*898C>T| |
S96 |
14 | BAA07g09910 | A07 | 18812518 | G | A | downstream_gene_variant | MODIFIER | c.*1130G>A| |
S267 |
15 | BAA07g09910 | A07 | 18813422 | C | T | downstream_gene_variant | MODIFIER | c.*2034C>T| |
S121 |
16 | BAA07g09910 | A07 | 18813665 | C | T | downstream_gene_variant | MODIFIER | c.*2277C>T| |
S247 |
17 | BAA07g09910 | A07 | 18813973 | G | A | downstream_gene_variant | MODIFIER | c.*2585G>A| |
S54 |