Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g21130 | A03 | 9573769 | G | A | downstream_gene_variant | MODIFIER | c.*2756C>T| |
S168 |
2 | BAA03g21130 | A03 | 9576553 | G | A | missense_variant | MODERATE | c.1268C>T|p.Ala423Val |
S132 S215 S89 |
3 | BAA03g21130 | A03 | 9576824 | G | A | missense_variant | MODERATE | c.997C>T|p.Leu333Phe |
S37 |
4 | BAA03g21130 | A03 | 9580775 | G | A | intron_variant | MODIFIER | c.597+2485C>T| |
S71 |
5 | BAA03g21130 | A03 | 9580931 | A | T | intron_variant | MODIFIER | c.597+2329T>A| |
S237 |
6 | BAA03g21130 | A03 | 9581388 | G | A | intron_variant | MODIFIER | c.597+1872C>T| |
S185 |
7 | BAA03g21130 | A03 | 9585433 | G | A | synonymous_variant | LOW | c.48C>T|p.Leu16Leu |
S261 |
8 | BAA03g21130 | A03 | 9586317 | G | A | upstream_gene_variant | MODIFIER | c.-837C>T| |
S17 |
9 | BAA03g21130 | A03 | 9589596 | C | T | upstream_gene_variant | MODIFIER | c.-4116G>A| |
S117 |
10 | BAA03g21130 | A03 | 9589987 | G | A | upstream_gene_variant | MODIFIER | c.-4507C>T| |
S123 |