Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26080 | A01 | 14470155 | G | A | stop_gained | HIGH | c.1216C>T|p.Gln406* |
S165 |
2 | BAA01g26080 | A01 | 14471392 | C | T | missense_variant | MODERATE | c.481G>A|p.Glu161Lys |
S183 |
3 | BAA01g26080 | A01 | 14471526 | G | A | missense_variant | MODERATE | c.419C>T|p.Thr140Ile |
S238 |
4 | BAA01g26080 | A01 | 14471965 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.129-1G>A| |
S208 S93 |
5 | BAA01g26080 | A01 | 14472086 | G | A | synonymous_variant | LOW | c.72C>T|p.Ser24Ser |
S84 S93 |
6 | BAA01g26080 | A01 | 14475477 | C | T | upstream_gene_variant | MODIFIER | c.-3320G>A| |
S38 |
7 | BAA01g26080 | A01 | 14475819 | G | A | upstream_gene_variant | MODIFIER | c.-3662C>T| |
S240 |
8 | BAA01g26080 | A01 | 14475994 | C | T | upstream_gene_variant | MODIFIER | c.-3837G>A| |
S134 |
9 | BAA01g26080 | A01 | 14476498 | C | T | upstream_gene_variant | MODIFIER | c.-4341G>A| |
S134 |
10 | BAA01g26080 | A01 | 14476566 | C | T | upstream_gene_variant | MODIFIER | c.-4409G>A| |
S176 |