Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26120 | A01 | 14506752 | C | T | upstream_gene_variant | MODIFIER | c.-4959C>T| |
S166 |
2 | BAA01g26120 | A01 | 14506768 | G | A | upstream_gene_variant | MODIFIER | c.-4943G>A| |
S57 |
3 | BAA01g26120 | A01 | 14508336 | A | C | upstream_gene_variant | MODIFIER | c.-3375A>C| |
S150 |
4 | BAA01g26120 | A01 | 14508427 | G | A | upstream_gene_variant | MODIFIER | c.-3284G>A| |
S188 |
5 | BAA01g26120 | A01 | 14509601 | G | A | upstream_gene_variant | MODIFIER | c.-2110G>A| |
S275 |
6 | BAA01g26120 | A01 | 14510526 | C | T | upstream_gene_variant | MODIFIER | c.-1185C>T| |
S265 |
7 | BAA01g26120 | A01 | 14511217 | C | T | upstream_gene_variant | MODIFIER | c.-494C>T| |
S256 |
8 | BAA01g26120 | A01 | 14512516 | G | A | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S103 |
9 | BAA01g26120 | A01 | 14512593 | C | T | synonymous_variant | LOW | c.783C>T|p.Leu261Leu |
S158 |
10 | BAA01g26120 | A01 | 14513436 | G | A | missense_variant | MODERATE | c.1576G>A|p.Asp526Asn |
S14 |
11 | BAA01g26120 | A01 | 14513646 | G | A | missense_variant | MODERATE | c.1786G>A|p.Val596Ile |
S72 S78 |
12 | BAA01g26120 | A01 | 14513795 | G | A | missense_variant | MODERATE | c.1935G>A|p.Met645Ile |
S274 |
13 | BAA01g26120 | A01 | 14514540 | C | T | missense_variant | MODERATE | c.2270C>T|p.Ala757Val |
S55 |
14 | BAA01g26120 | A01 | 14514739 | G | A | missense_variant | MODERATE | c.2469G>A|p.Met823Ile |
S187 |
15 | BAA01g26120 | A01 | 14514764 | G | A | missense_variant | MODERATE | c.2494G>A|p.Val832Ile |
S298 |
16 | BAA01g26120 | A01 | 14514876 | C | T | missense_variant | MODERATE | c.2606C>T|p.Ala869Val |
S249 |
17 | BAA01g26120 | A01 | 14514885 | G | A | missense_variant | MODERATE | c.2615G>A|p.Arg872His |
S58 |
18 | BAA01g26120 | A01 | 14515083 | G | A | missense_variant | MODERATE | c.2813G>A|p.Gly938Glu |
S240 |
19 | BAA01g26120 | A01 | 14515187 | G | A | missense_variant | MODERATE | c.2831G>A|p.Ser944Asn |
S59 |