Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g36770 | A07 | 34187322 | C | T | upstream_gene_variant | MODIFIER | c.-4844C>T| |
S274 |
2 | BAA07g36770 | A07 | 34187631 | C | T | upstream_gene_variant | MODIFIER | c.-4535C>T| |
S159 S243 S299 |
3 | BAA07g36770 | A07 | 34187928 | G | A | upstream_gene_variant | MODIFIER | c.-4238G>A| |
S271 |
4 | BAA07g36770 | A07 | 34190150 | G | A | upstream_gene_variant | MODIFIER | c.-2016G>A| |
S38 |
5 | BAA07g36770 | A07 | 34192207 | G | A | synonymous_variant | LOW | c.42G>A|p.Gln14Gln |
S267 |
6 | BAA07g36770 | A07 | 34192288 | C | T | synonymous_variant | LOW | c.123C>T|p.Phe41Phe |
S177 |
7 | BAA07g36770 | A07 | 34193315 | G | A | missense_variant | MODERATE | c.1150G>A|p.Asp384Asn |
S17 |
8 | BAA07g36770 | A07 | 34193348 | C | T | missense_variant | MODERATE | c.1183C>T|p.Pro395Ser |
S168 |
9 | BAA07g36770 | A07 | 34193536 | C | T | missense_variant | MODERATE | c.1286C>T|p.Ser429Leu |
S275 |
10 | BAA07g36770 | A07 | 34195871 | G | A | downstream_gene_variant | MODIFIER | c.*1652G>A| |
S257 |