Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30370 | A08 | 20548778 | C | T | missense_variant | MODERATE | c.146C>T|p.Ser49Phe |
S209 |
2 | BAA08g30370 | A08 | 20549075 | C | T | synonymous_variant | LOW | c.259C>T|p.Leu87Leu |
S185 |
3 | BAA08g30370 | A08 | 20549899 | C | T | stop_gained | HIGH | c.982C>T|p.Gln328* |
S130 |
4 | BAA08g30370 | A08 | 20551057 | C | T | splice_region_variant&synonymous_variant | LOW | c.1824C>T|p.Ile608Ile |
S271 |
5 | BAA08g30370 | A08 | 20551445 | C | T | missense_variant | MODERATE | c.1901C>T|p.Ser634Phe |
S129 |
6 | BAA08g30370 | A08 | 20552191 | G | A | missense_variant | MODERATE | c.2647G>A|p.Val883Ile |
S170 |
7 | BAA08g30370 | A08 | 20553302 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.3550-1G>A| |
S69 |
8 | BAA08g30370 | A08 | 20553915 | C | T | missense_variant | MODERATE | c.3953C>T|p.Ala1318Val |
S208 S219 |
9 | BAA08g30370 | A08 | 20553966 | C | T | missense_variant | MODERATE | c.4004C>T|p.Thr1335Ile |
S173 |
10 | BAA08g30370 | A08 | 20557211 | G | A | downstream_gene_variant | MODIFIER | c.*3196G>A| |
S10 |