Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18590 | A08 | 14842044 | C | T | upstream_gene_variant | MODIFIER | c.-4537C>T| |
S210 |
2 | BAA08g18590 | A08 | 14842171 | G | A | upstream_gene_variant | MODIFIER | c.-4410G>A| |
S193 |
3 | BAA08g18590 | A08 | 14843108 | G | A | upstream_gene_variant | MODIFIER | c.-3473G>A| |
S172 |
4 | BAA08g18590 | A08 | 14843109 | C | T | upstream_gene_variant | MODIFIER | c.-3472C>T| |
S223 |
5 | BAA08g18590 | A08 | 14843602 | C | T | upstream_gene_variant | MODIFIER | c.-2979C>T| |
S293 |
6 | BAA08g18590 | A08 | 14844573 | C | T | upstream_gene_variant | MODIFIER | c.-2008C>T| |
S168 |
7 | BAA08g18590 | A08 | 14844933 | G | A | upstream_gene_variant | MODIFIER | c.-1648G>A| |
S273 |
8 | BAA08g18590 | A08 | 14845166 | G | A | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S65 |
9 | BAA08g18590 | A08 | 14845513 | C | T | upstream_gene_variant | MODIFIER | c.-1068C>T| |
S88 |
10 | BAA08g18590 | A08 | 14847913 | G | A | missense_variant | MODERATE | c.803G>A|p.Ser268Asn |
S279 |
11 | BAA08g18590 | A08 | 14848088 | C | T | synonymous_variant | LOW | c.894C>T|p.Phe298Phe |
S251 |