Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30390 | A08 | 20556626 | C | T | missense_variant | MODERATE | c.1871G>A|p.Gly624Asp |
S173 |
2 | BAA08g30390 | A08 | 20556679 | C | T | synonymous_variant | LOW | c.1818G>A|p.Lys606Lys |
S206 S26 |
3 | BAA08g30390 | A08 | 20556690 | C | T | missense_variant | MODERATE | c.1807G>A|p.Ala603Thr |
S50 |
4 | BAA08g30390 | A08 | 20557647 | C | T | missense_variant | MODERATE | c.1241G>A|p.Gly414Asp |
S130 S47 |
5 | BAA08g30390 | A08 | 20558619 | G | A | missense_variant | MODERATE | c.716C>T|p.Ser239Phe |
S238 |
6 | BAA08g30390 | A08 | 20558882 | G | A | synonymous_variant | LOW | c.453C>T|p.Leu151Leu |
S100 |
7 | BAA08g30390 | A08 | 20559350 | C | T | missense_variant | MODERATE | c.193G>A|p.Glu65Lys |
S6 |
8 | BAA08g30390 | A08 | 20559648 | T | A | upstream_gene_variant | MODIFIER | c.-106A>T| |
S256 |
9 | BAA08g30390 | A08 | 20560441 | G | A | upstream_gene_variant | MODIFIER | c.-899C>T| |
S40 S49 |
10 | BAA08g30390 | A08 | 20560459 | G | A | upstream_gene_variant | MODIFIER | c.-917C>T| |
S289 S290 |
11 | BAA08g30390 | A08 | 20561057 | C | T | upstream_gene_variant | MODIFIER | c.-1515G>A| |
S305 |
12 | BAA08g30390 | A08 | 20561076 | G | A | upstream_gene_variant | MODIFIER | c.-1534C>T| |
S34 |
13 | BAA08g30390 | A08 | 20562386 | G | A | upstream_gene_variant | MODIFIER | c.-2844C>T| |
S40 S49 |
14 | BAA08g30390 | A08 | 20563232 | C | T | upstream_gene_variant | MODIFIER | c.-3690G>A| |
S293 |
15 | BAA08g30390 | A08 | 20563985 | C | T | upstream_gene_variant | MODIFIER | c.-4443G>A| |
S152 |