Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g37860 | A01 | 25298300 | C | T | upstream_gene_variant | MODIFIER | c.-2708C>T| |
S127 |
2 | BAA01g37860 | A01 | 25299376 | G | A | upstream_gene_variant | MODIFIER | c.-1632G>A| |
S284 |
3 | BAA01g37860 | A01 | 25299742 | G | A | upstream_gene_variant | MODIFIER | c.-1266G>A| |
S298 S42 |
4 | BAA01g37860 | A01 | 25299762 | C | T | upstream_gene_variant | MODIFIER | c.-1246C>T| |
S46 |
5 | BAA01g37860 | A01 | 25300145 | G | A | upstream_gene_variant | MODIFIER | c.-863G>A| |
S306 S308 |
6 | BAA01g37860 | A01 | 25300197 | C | T | upstream_gene_variant | MODIFIER | c.-811C>T| |
S177 |
7 | BAA01g37860 | A01 | 25300868 | C | T | upstream_gene_variant | MODIFIER | c.-140C>T| |
S274 |
8 | BAA01g37860 | A01 | 25301977 | C | T | missense_variant | MODERATE | c.289C>T|p.Pro97Ser |
S216 |
9 | BAA01g37860 | A01 | 25301981 | C | T | missense_variant | MODERATE | c.293C>T|p.Thr98Ile |
S92 |
10 | BAA01g37860 | A01 | 25302755 | C | T | intron_variant | MODIFIER | c.595-36C>T| |
S305 |
11 | BAA01g37860 | A01 | 25302787 | C | T | splice_region_variant&intron_variant | LOW | c.595-4C>T| |
S293 |
12 | BAA01g37860 | A01 | 25302806 | C | T | synonymous_variant | LOW | c.610C>T|p.Leu204Leu |
S153 |
13 | BAA01g37860 | A01 | 25303051 | G | A | missense_variant | MODERATE | c.754G>A|p.Glu252Lys |
S33 |
14 | BAA01g37860 | A01 | 25303101 | C | T | intron_variant | MODIFIER | c.774+30C>T| |
S303 |
15 | BAA01g37860 | A01 | 25304427 | G | A | synonymous_variant | LOW | c.1494G>A|p.Thr498Thr |
S181 |
16 | BAA01g37860 | A01 | 25304640 | C | T | missense_variant | MODERATE | c.1630C>T|p.Pro544Ser |
S46 |
17 | BAA01g37860 | A01 | 25304706 | G | A | missense_variant | MODERATE | c.1696G>A|p.Val566Met |
S125 |