Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06450 | A01 | 2881583 | C | T | missense_variant | MODERATE | c.2003G>A|p.Arg668Lys |
S155 S211 |
2 | BAA01g06450 | A01 | 2881759 | G | A | intron_variant | MODIFIER | c.1921-94C>T| |
S142 |
3 | BAA01g06450 | A01 | 2882013 | G | A | intron_variant | MODIFIER | c.1920+31C>T| |
S262 |
4 | BAA01g06450 | A01 | 2882858 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1502-1G>A| |
S139 |
5 | BAA01g06450 | A01 | 2884593 | G | A | missense_variant | MODERATE | c.689C>T|p.Thr230Ile |
S60 |
6 | BAA01g06450 | A01 | 2885028 | C | T | synonymous_variant | LOW | c.339G>A|p.Ala113Ala |
S265 |
7 | BAA01g06450 | A01 | 2887865 | C | T | upstream_gene_variant | MODIFIER | c.-2151G>A| |
S278 |
8 | BAA01g06450 | A01 | 2890686 | C | T | upstream_gene_variant | MODIFIER | c.-4972G>A| |
S237 |