Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07930 | A05 | 3966546 | G | A | missense_variant | MODERATE | c.857C>T|p.Ala286Val |
S115 |
2 | BAA05g07930 | A05 | 3966867 | C | T | missense_variant | MODERATE | c.697G>A|p.Val233Ile |
S113 |
3 | BAA05g07930 | A05 | 3967155 | G | A | missense_variant | MODERATE | c.565C>T|p.Leu189Phe |
S62 |
4 | BAA05g07930 | A05 | 3968343 | C | T | synonymous_variant | LOW | c.42G>A|p.Lys14Lys |
S196 |
5 | BAA05g07930 | A05 | 3968439 | C | T | splice_region_variant&synonymous_variant | LOW | c.33G>A|p.Lys11Lys |
S265 |
6 | BAA05g07930 | A05 | 3968483 | C | T | upstream_gene_variant | MODIFIER | c.-12G>A| |
S191 |
7 | BAA05g07930 | A05 | 3968625 | G | A | upstream_gene_variant | MODIFIER | c.-154C>T| |
S268 |
8 | BAA05g07930 | A05 | 3968827 | G | A | upstream_gene_variant | MODIFIER | c.-356C>T| |
S301 S304 |
9 | BAA05g07930 | A05 | 3968915 | C | T | upstream_gene_variant | MODIFIER | c.-444G>A| |
S172 S217 |
10 | BAA05g07930 | A05 | 3969687 | G | A | upstream_gene_variant | MODIFIER | c.-1216C>T| |
S170 |
11 | BAA05g07930 | A05 | 3970609 | G | A | upstream_gene_variant | MODIFIER | c.-2138C>T| |
S111 |
12 | BAA05g07930 | A05 | 3971644 | C | T | upstream_gene_variant | MODIFIER | c.-3173G>A| |
S146 |
13 | BAA05g07930 | A05 | 3971992 | G | A | upstream_gene_variant | MODIFIER | c.-3521C>T| |
S139 |
14 | BAA05g07930 | A05 | 3972051 | G | A | upstream_gene_variant | MODIFIER | c.-3580C>T| |
S64 |