Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26430 | A09 | 17172710 | C | T | upstream_gene_variant | MODIFIER | c.-843C>T| |
S16 |
2 | BAA09g26430 | A09 | 17173073 | C | T | upstream_gene_variant | MODIFIER | c.-480C>T| |
S231 |
3 | BAA09g26430 | A09 | 17173357 | G | A | upstream_gene_variant | MODIFIER | c.-196G>A| |
S127 S28 |
4 | BAA09g26430 | A09 | 17173879 | C | T | synonymous_variant | LOW | c.327C>T|p.Ile109Ile |
S206 S26 |
5 | BAA09g26430 | A09 | 17174208 | G | A | missense_variant | MODERATE | c.656G>A|p.Gly219Asp |
S124 |
6 | BAA09g26430 | A09 | 17174338 | C | T | synonymous_variant | LOW | c.786C>T|p.Gly262Gly |
S151 S263 |
7 | BAA09g26430 | A09 | 17174395 | C | T | synonymous_variant | LOW | c.843C>T|p.Phe281Phe |
S124 S99 |
8 | BAA09g26430 | A09 | 17174698 | C | T | synonymous_variant | LOW | c.1146C>T|p.Ile382Ile |
S41 |
9 | BAA09g26430 | A09 | 17174789 | G | A | missense_variant | MODERATE | c.1237G>A|p.Asp413Asn |
S182 |
10 | BAA09g26430 | A09 | 17174955 | G | A | missense_variant | MODERATE | c.1403G>A|p.Gly468Asp |
S155 S211 |
11 | BAA09g26430 | A09 | 17175333 | C | T | downstream_gene_variant | MODIFIER | c.*43C>T| |
S247 |
12 | BAA09g26430 | A09 | 17175541 | C | T | downstream_gene_variant | MODIFIER | c.*251C>T| |
S270 |
13 | BAA09g26430 | A09 | 17175701 | G | A | downstream_gene_variant | MODIFIER | c.*411G>A| |
S201 |
14 | BAA09g26430 | A09 | 17177109 | C | T | downstream_gene_variant | MODIFIER | c.*1819C>T| |
S118 |