Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46090 | A01 | 30705553 | G | A | missense_variant | MODERATE | c.3182C>T|p.Thr1061Ile |
S197 |
2 | BAA01g46090 | A01 | 30706499 | C | T | missense_variant | MODERATE | c.2648G>A|p.Gly883Asp |
S77 |
3 | BAA01g46090 | A01 | 30709169 | C | T | synonymous_variant | LOW | c.1326G>A|p.Arg442Arg |
S206 S26 |
4 | BAA01g46090 | A01 | 30709384 | G | A | intron_variant | MODIFIER | c.1215-104C>T| |
S121 |
5 | BAA01g46090 | A01 | 30711687 | G | A | intron_variant | MODIFIER | c.786+30C>T| |
S272 |
6 | BAA01g46090 | A01 | 30711971 | C | T | intron_variant | MODIFIER | c.696+108G>A| |
S156 |
7 | BAA01g46090 | A01 | 30712760 | C | T | missense_variant | MODERATE | c.448G>A|p.Val150Ile |
S249 |
8 | BAA01g46090 | A01 | 30713936 | C | T | upstream_gene_variant | MODIFIER | c.-395G>A| |
S167 |
9 | BAA01g46090 | A01 | 30714377 | G | A | upstream_gene_variant | MODIFIER | c.-836C>T| |
S115 |
10 | BAA01g46090 | A01 | 30714771 | G | A | upstream_gene_variant | MODIFIER | c.-1230C>T| |
S136 |
11 | BAA01g46090 | A01 | 30714837 | C | T | upstream_gene_variant | MODIFIER | c.-1296G>A| |
S182 |
12 | BAA01g46090 | A01 | 30715099 | G | A | upstream_gene_variant | MODIFIER | c.-1558C>T| |
S274 |
13 | BAA01g46090 | A01 | 30718424 | C | T | upstream_gene_variant | MODIFIER | c.-4883G>A| |
S23 |