Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g27720 | A05 | 31871928 | C | T | missense_variant | MODERATE | c.3323G>A|p.Gly1108Glu |
S152 |
2 | BAA05g27720 | A05 | 31872376 | G | A | missense_variant | MODERATE | c.2875C>T|p.Leu959Phe |
S138 |
3 | BAA05g27720 | A05 | 31872993 | C | T | synonymous_variant | LOW | c.2529G>A|p.Gly843Gly |
S288 |
4 | BAA05g27720 | A05 | 31873236 | C | T | missense_variant | MODERATE | c.2371G>A|p.Glu791Lys |
S162 |
5 | BAA05g27720 | A05 | 31873601 | G | A | stop_gained | HIGH | c.2098C>T|p.Gln700* |
S151 S263 |
6 | BAA05g27720 | A05 | 31873637 | C | T | intron_variant | MODIFIER | c.2077-15G>A| |
S192 |
7 | BAA05g27720 | A05 | 31874423 | T | A | intron_variant | MODIFIER | c.1711-46A>T| |
S293 |
8 | BAA05g27720 | A05 | 31875866 | G | A | intron_variant | MODIFIER | c.1131+9C>T| |
S131 |
9 | BAA05g27720 | A05 | 31876543 | G | A | synonymous_variant | LOW | c.852C>T|p.Asn284Asn |
S185 |
10 | BAA05g27720 | A05 | 31876635 | G | A | missense_variant | MODERATE | c.760C>T|p.Leu254Phe |
S296 |
11 | BAA05g27720 | A05 | 31876694 | C | T | missense_variant&splice_region_variant | MODERATE | c.701G>A|p.Gly234Asp |
S294 |
12 | BAA05g27720 | A05 | 31878642 | G | A | upstream_gene_variant | MODIFIER | c.-810C>T| |
S172 S217 |
13 | BAA05g27720 | A05 | 31878768 | C | T | upstream_gene_variant | MODIFIER | c.-936G>A| |
S287 |
14 | BAA05g27720 | A05 | 31879059 | G | A | upstream_gene_variant | MODIFIER | c.-1227C>T| |
S6 |
15 | BAA05g27720 | A05 | 31879628 | G | A | upstream_gene_variant | MODIFIER | c.-1796C>T| |
S252 |
16 | BAA05g27720 | A05 | 31881493 | C | T | upstream_gene_variant | MODIFIER | c.-3661G>A| |
S25 |
17 | BAA05g27720 | A05 | 31881689 | C | T | upstream_gene_variant | MODIFIER | c.-3857G>A| |
S297 |
18 | BAA05g27720 | A05 | 31881868 | C | T | upstream_gene_variant | MODIFIER | c.-4036G>A| |
S18 |