Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02170 | A08 | 1537531 | C | T | upstream_gene_variant | MODIFIER | c.-2405C>T| |
S261 |
2 | BAA08g02170 | A08 | 1537639 | C | T | upstream_gene_variant | MODIFIER | c.-2297C>T| |
S275 |
3 | BAA08g02170 | A08 | 1538518 | T | A | upstream_gene_variant | MODIFIER | c.-1418T>A| |
S195 |
4 | BAA08g02170 | A08 | 1539931 | C | T | upstream_gene_variant | MODIFIER | c.-5C>T| |
S203 |
5 | BAA08g02170 | A08 | 1539938 | G | A | start_lost | HIGH | c.3G>A|p.Met1? |
S179 |
6 | BAA08g02170 | A08 | 1540966 | G | A | missense_variant | MODERATE | c.314G>A|p.Gly105Glu |
S181 |
7 | BAA08g02170 | A08 | 1542275 | G | A | downstream_gene_variant | MODIFIER | c.*1143G>A| |
S41 |
8 | BAA08g02170 | A08 | 1542359 | G | A | downstream_gene_variant | MODIFIER | c.*1227G>A| |
S206 |
9 | BAA08g02170 | A08 | 1545723 | G | T | downstream_gene_variant | MODIFIER | c.*4591G>T| |
S162 |