Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08500 | A04 | 5850668 | C | T | upstream_gene_variant | MODIFIER | c.-4452C>T| |
S23 |
2 | BAA04g08500 | A04 | 5851133 | C | T | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S174 |
3 | BAA04g08500 | A04 | 5856392 | G | A | missense_variant | MODERATE | c.1186G>A|p.Glu396Lys |
S190 |
4 | BAA04g08500 | A04 | 5856713 | G | A | missense_variant | MODERATE | c.1507G>A|p.Glu503Lys |
S67 |
5 | BAA04g08500 | A04 | 5857189 | G | A | synonymous_variant | LOW | c.1983G>A|p.Gln661Gln |
S262 |
6 | BAA04g08500 | A04 | 5857317 | G | A | missense_variant | MODERATE | c.2111G>A|p.Gly704Glu |
S65 |
7 | BAA04g08500 | A04 | 5857697 | G | A | missense_variant | MODERATE | c.2491G>A|p.Asp831Asn |
S124 |
8 | BAA04g08500 | A04 | 5857808 | C | T | missense_variant | MODERATE | c.2602C>T|p.His868Tyr |
S15 S156 S3 S34 S4 S6 |
9 | BAA04g08500 | A04 | 5859064 | C | T | downstream_gene_variant | MODIFIER | c.*681C>T| |
S242 |
10 | BAA04g08500 | A04 | 5860502 | C | T | downstream_gene_variant | MODIFIER | c.*2119C>T| |
S209 |