Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28900 | A01 | 18199188 | G | A | upstream_gene_variant | MODIFIER | c.-3244G>A| |
S114 |
2 | BAA01g28900 | A01 | 18199280 | G | A | upstream_gene_variant | MODIFIER | c.-3152G>A| |
S83 S88 |
3 | BAA01g28900 | A01 | 18199329 | C | T | upstream_gene_variant | MODIFIER | c.-3103C>T| |
S94 |
4 | BAA01g28900 | A01 | 18199395 | C | T | upstream_gene_variant | MODIFIER | c.-3037C>T| |
S303 |
5 | BAA01g28900 | A01 | 18199520 | G | A | upstream_gene_variant | MODIFIER | c.-2912G>A| |
S23 |
6 | BAA01g28900 | A01 | 18201039 | C | T | upstream_gene_variant | MODIFIER | c.-1393C>T| |
S250 |
7 | BAA01g28900 | A01 | 18201442 | G | A | upstream_gene_variant | MODIFIER | c.-990G>A| |
S161 |
8 | BAA01g28900 | A01 | 18202769 | G | A | intron_variant | MODIFIER | c.190-51G>A| |
S296 |
9 | BAA01g28900 | A01 | 18203154 | C | T | intron_variant | MODIFIER | c.373+38C>T| |
S56 |
10 | BAA01g28900 | A01 | 18203413 | C | T | intron_variant | MODIFIER | c.373+297C>T| |
S39 |
11 | BAA01g28900 | A01 | 18203526 | C | T | intron_variant | MODIFIER | c.373+410C>T| |
S198 |
12 | BAA01g28900 | A01 | 18203585 | C | T | intron_variant | MODIFIER | c.373+469C>T| |
S210 S225 |
13 | BAA01g28900 | A01 | 18206187 | G | A | missense_variant | MODERATE | c.904G>A|p.Asp302Asn |
S100 |
14 | BAA01g28900 | A01 | 18210681 | G | A | downstream_gene_variant | MODIFIER | c.*4291G>A| |
S174 S216 |
15 | BAA01g28900 | A01 | 18210712 | G | A | downstream_gene_variant | MODIFIER | c.*4322G>A| |
S257 |
16 | BAA01g28900 | A01 | 18211051 | G | A | downstream_gene_variant | MODIFIER | c.*4661G>A| |
S263 |