Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23020 | A08 | 17132387 | C | T | synonymous_variant | LOW | c.1740G>A|p.Gln580Gln |
S106 |
2 | BAA08g23020 | A08 | 17133197 | G | A | missense_variant | MODERATE | c.1237C>T|p.Pro413Ser |
S229 |
3 | BAA08g23020 | A08 | 17133353 | C | T | missense_variant&splice_region_variant | MODERATE | c.1211G>A|p.Gly404Asp |
S173 |
4 | BAA08g23020 | A08 | 17135554 | G | A | synonymous_variant | LOW | c.297C>T|p.Asp99Asp |
S162 |
5 | BAA08g23020 | A08 | 17135566 | C | T | synonymous_variant | LOW | c.285G>A|p.Gly95Gly |
S245 |
6 | BAA08g23020 | A08 | 17137653 | C | T | upstream_gene_variant | MODIFIER | c.-1480G>A| |
S299 |
7 | BAA08g23020 | A08 | 17138165 | C | T | upstream_gene_variant | MODIFIER | c.-1992G>A| |
S234 |
8 | BAA08g23020 | A08 | 17138182 | G | A | upstream_gene_variant | MODIFIER | c.-2009C>T| |
S86 |
9 | BAA08g23020 | A08 | 17140057 | C | T | upstream_gene_variant | MODIFIER | c.-3884G>A| |
S212 |
10 | BAA08g23020 | A08 | 17140083 | C | T | upstream_gene_variant | MODIFIER | c.-3910G>A| |
S278 |