Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g03430 | A04 | 2100860 | G | A | upstream_gene_variant | MODIFIER | c.-3716G>A| |
S159 S188 S243 S276 S298 S299 |
2 | BAA04g03430 | A04 | 2103181 | C | T | upstream_gene_variant | MODIFIER | c.-1395C>T| |
S231 |
3 | BAA04g03430 | A04 | 2104042 | G | A | upstream_gene_variant | MODIFIER | c.-534G>A| |
S188 |
4 | BAA04g03430 | A04 | 2104793 | G | A | missense_variant | MODERATE | c.218G>A|p.Gly73Asp |
S188 |
5 | BAA04g03430 | A04 | 2107324 | C | T | missense_variant | MODERATE | c.740C>T|p.Ala247Val |
S20 |
6 | BAA04g03430 | A04 | 2107387 | C | T | missense_variant | MODERATE | c.803C>T|p.Thr268Ile |
S289 S290 |
7 | BAA04g03430 | A04 | 2107871 | G | A | splice_donor_variant&intron_variant | HIGH | c.1200+1G>A| |
S160 |
8 | BAA04g03430 | A04 | 2108887 | G | A | intron_variant | MODIFIER | c.1200+1017G>A| |
S282 |
9 | BAA04g03430 | A04 | 2109163 | C | T | intron_variant | MODIFIER | c.1201-875C>T| |
S148 |