Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46000 | A09 | 50961118 | C | T | synonymous_variant | LOW | c.2013G>A|p.Ala671Ala |
S95 |
2 | BAA09g46000 | A09 | 50962691 | G | A | missense_variant | MODERATE | c.1346C>T|p.Ser449Leu |
S216 |
3 | BAA09g46000 | A09 | 50963339 | G | A | missense_variant | MODERATE | c.1114C>T|p.Pro372Ser |
S36 |
4 | BAA09g46000 | A09 | 50963814 | C | T | missense_variant | MODERATE | c.724G>A|p.Glu242Lys |
S67 |
5 | BAA09g46000 | A09 | 50963863 | C | T | splice_region_variant&intron_variant | LOW | c.679-4G>A| |
S208 S219 |
6 | BAA09g46000 | A09 | 50964609 | G | A | missense_variant | MODERATE | c.107C>T|p.Ala36Val |
S57 |
7 | BAA09g46000 | A09 | 50965267 | C | A | upstream_gene_variant | MODIFIER | c.-552G>T| |
S189 S226 S250 S291 |
8 | BAA09g46000 | A09 | 50965579 | G | A | upstream_gene_variant | MODIFIER | c.-864C>T| |
S36 |
9 | BAA09g46000 | A09 | 50966208 | C | T | upstream_gene_variant | MODIFIER | c.-1493G>A| |
S5 |
10 | BAA09g46000 | A09 | 50966871 | C | T | upstream_gene_variant | MODIFIER | c.-2156G>A| |
S169 |
11 | BAA09g46000 | A09 | 50967998 | G | A | upstream_gene_variant | MODIFIER | c.-3283C>T| |
S188 |
12 | BAA09g46000 | A09 | 50968006 | G | A | upstream_gene_variant | MODIFIER | c.-3291C>T| |
S246 |