Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03890 | A01 | 1763386 | C | T | upstream_gene_variant | MODIFIER | c.-4578C>T| |
S88 |
2 | BAA01g03890 | A01 | 1765461 | G | A | upstream_gene_variant | MODIFIER | c.-2503G>A| |
S251 |
3 | BAA01g03890 | A01 | 1765804 | G | A | upstream_gene_variant | MODIFIER | c.-2160G>A| |
S274 |
4 | BAA01g03890 | A01 | 1766538 | C | T | upstream_gene_variant | MODIFIER | c.-1426C>T| |
S19 |
5 | BAA01g03890 | A01 | 1767635 | G | A | upstream_gene_variant | MODIFIER | c.-329G>A| |
S7 |
6 | BAA01g03890 | A01 | 1768016 | G | A | missense_variant | MODERATE | c.53G>A|p.Ser18Asn |
S306 S308 |
7 | BAA01g03890 | A01 | 1768039 | C | T | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S246 |
8 | BAA01g03890 | A01 | 1768097 | C | T | missense_variant | MODERATE | c.134C>T|p.Ser45Phe |
S244 |
9 | BAA01g03890 | A01 | 1768130 | C | T | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S43 |
10 | BAA01g03890 | A01 | 1768199 | C | T | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S53 |
11 | BAA01g03890 | A01 | 1768356 | C | T | synonymous_variant | LOW | c.393C>T|p.Asp131Asp |
S155 S211 |
12 | BAA01g03890 | A01 | 1771683 | G | A | downstream_gene_variant | MODIFIER | c.*2643G>A| |
S250 |