Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22140 | A02 | 11926993 | G | A | upstream_gene_variant | MODIFIER | c.-4812G>A| |
S33 |
2 | BAA02g22140 | A02 | 11927058 | G | A | upstream_gene_variant | MODIFIER | c.-4747G>A| |
S12 |
3 | BAA02g22140 | A02 | 11927375 | G | A | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S7 |
4 | BAA02g22140 | A02 | 11927963 | G | A | upstream_gene_variant | MODIFIER | c.-3842G>A| |
S184 |
5 | BAA02g22140 | A02 | 11928719 | G | A | upstream_gene_variant | MODIFIER | c.-3086G>A| |
S43 |
6 | BAA02g22140 | A02 | 11929158 | C | T | upstream_gene_variant | MODIFIER | c.-2647C>T| |
S82 S92 |
7 | BAA02g22140 | A02 | 11929460 | C | T | upstream_gene_variant | MODIFIER | c.-2345C>T| |
S81 |
8 | BAA02g22140 | A02 | 11929707 | C | T | upstream_gene_variant | MODIFIER | c.-2098C>T| |
S185 |
9 | BAA02g22140 | A02 | 11930766 | G | A | upstream_gene_variant | MODIFIER | c.-1039G>A| |
S297 |
10 | BAA02g22140 | A02 | 11930880 | C | T | upstream_gene_variant | MODIFIER | c.-925C>T| |
S250 |
11 | BAA02g22140 | A02 | 11931324 | C | T | upstream_gene_variant | MODIFIER | c.-481C>T| |
S84 S93 |
12 | BAA02g22140 | A02 | 11931790 | G | A | upstream_gene_variant | MODIFIER | c.-15G>A| |
S237 |
13 | BAA02g22140 | A02 | 11931982 | G | A | missense_variant | MODERATE | c.178G>A|p.Asp60Asn |
S132 S215 |
14 | BAA02g22140 | A02 | 11932515 | G | A | missense_variant | MODERATE | c.632G>A|p.Arg211Lys |
S281 |
15 | BAA02g22140 | A02 | 11932679 | C | T | splice_region_variant&intron_variant | LOW | c.700-3C>T| |
S1 S90 |
16 | BAA02g22140 | A02 | 11933439 | G | A | missense_variant | MODERATE | c.1206G>A|p.Met402Ile |
S202 |