Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11270 | A01 | 5200190 | G | A | downstream_gene_variant | MODIFIER | c.*3184C>T| |
S263 |
2 | BAA01g11270 | A01 | 5200265 | G | A | downstream_gene_variant | MODIFIER | c.*3109C>T| |
S74 |
3 | BAA01g11270 | A01 | 5200540 | G | A | downstream_gene_variant | MODIFIER | c.*2834C>T| |
S190 |
4 | BAA01g11270 | A01 | 5200662 | G | A | downstream_gene_variant | MODIFIER | c.*2712C>T| |
S197 |
5 | BAA01g11270 | A01 | 5200667 | C | T | downstream_gene_variant | MODIFIER | c.*2707G>A| |
S118 |
6 | BAA01g11270 | A01 | 5200945 | C | T | downstream_gene_variant | MODIFIER | c.*2429G>A| |
S128 |
7 | BAA01g11270 | A01 | 5202730 | C | T | downstream_gene_variant | MODIFIER | c.*644G>A| |
S291 S80 |
8 | BAA01g11270 | A01 | 5203129 | G | A | downstream_gene_variant | MODIFIER | c.*245C>T| |
S3 |
9 | BAA01g11270 | A01 | 5203170 | C | T | downstream_gene_variant | MODIFIER | c.*204G>A| |
S109 |
10 | BAA01g11270 | A01 | 5203601 | C | T | missense_variant | MODERATE | c.418G>A|p.Asp140Asn |
S291 |
11 | BAA01g11270 | A01 | 5204158 | G | A | missense_variant | MODERATE | c.88C>T|p.Leu30Phe |
S104 S52 |
12 | BAA01g11270 | A01 | 5205044 | A | T | upstream_gene_variant | MODIFIER | c.-799T>A| |
S186 |
13 | BAA01g11270 | A01 | 5205262 | C | T | upstream_gene_variant | MODIFIER | c.-1017G>A| |
S155 S211 |
14 | BAA01g11270 | A01 | 5206104 | G | A | upstream_gene_variant | MODIFIER | c.-1859C>T| |
S183 |
15 | BAA01g11270 | A01 | 5207147 | C | T | upstream_gene_variant | MODIFIER | c.-2902G>A| |
S177 |
16 | BAA01g11270 | A01 | 5208152 | C | T | upstream_gene_variant | MODIFIER | c.-3907G>A| |
S136 |
17 | BAA01g11270 | A01 | 5209176 | C | T | upstream_gene_variant | MODIFIER | c.-4931G>A| |
S118 |