Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12040 | A07 | 20506130 | C | T | upstream_gene_variant | MODIFIER | c.-4356C>T| |
S86 |
2 | BAA07g12040 | A07 | 20506216 | C | T | upstream_gene_variant | MODIFIER | c.-4270C>T| |
S32 |
3 | BAA07g12040 | A07 | 20506260 | C | T | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S179 |
4 | BAA07g12040 | A07 | 20507222 | C | T | upstream_gene_variant | MODIFIER | c.-3264C>T| |
S18 |
5 | BAA07g12040 | A07 | 20507445 | G | A | upstream_gene_variant | MODIFIER | c.-3041G>A| |
S183 |
6 | BAA07g12040 | A07 | 20507526 | G | A | upstream_gene_variant | MODIFIER | c.-2960G>A| |
S140 |
7 | BAA07g12040 | A07 | 20507872 | C | T | upstream_gene_variant | MODIFIER | c.-2614C>T| |
S79 S91 |
8 | BAA07g12040 | A07 | 20508847 | G | A | upstream_gene_variant | MODIFIER | c.-1639G>A| |
S44 |
9 | BAA07g12040 | A07 | 20509043 | G | A | upstream_gene_variant | MODIFIER | c.-1443G>A| |
S138 |
10 | BAA07g12040 | A07 | 20509127 | G | A | upstream_gene_variant | MODIFIER | c.-1359G>A| |
S229 |
11 | BAA07g12040 | A07 | 20509158 | C | T | upstream_gene_variant | MODIFIER | c.-1328C>T| |
S155 S211 |
12 | BAA07g12040 | A07 | 20509367 | C | A | upstream_gene_variant | MODIFIER | c.-1119C>A| |
S198 |
13 | BAA07g12040 | A07 | 20509527 | C | T | upstream_gene_variant | MODIFIER | c.-959C>T| |
S162 |
14 | BAA07g12040 | A07 | 20509996 | G | A | upstream_gene_variant | MODIFIER | c.-490G>A| |
S119 |
15 | BAA07g12040 | A07 | 20510067 | G | A | upstream_gene_variant | MODIFIER | c.-419G>A| |
S172 |
16 | BAA07g12040 | A07 | 20510312 | C | T | upstream_gene_variant | MODIFIER | c.-174C>T| |
S286 |
17 | BAA07g12040 | A07 | 20510671 | C | T | synonymous_variant | LOW | c.186C>T|p.Ile62Ile |
S35 |
18 | BAA07g12040 | A07 | 20512611 | C | T | missense_variant | MODERATE | c.1465C>T|p.Pro489Ser |
S36 |