Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20210 | A10 | 18272424 | C | T | upstream_gene_variant | MODIFIER | c.-4815C>T| |
S155 S211 |
2 | BAA10g20210 | A10 | 18272821 | C | T | upstream_gene_variant | MODIFIER | c.-4418C>T| |
S249 |
3 | BAA10g20210 | A10 | 18274215 | G | A | upstream_gene_variant | MODIFIER | c.-3024G>A| |
S164 |
4 | BAA10g20210 | A10 | 18275887 | C | T | upstream_gene_variant | MODIFIER | c.-1352C>T| |
S117 |
5 | BAA10g20210 | A10 | 18276878 | C | T | upstream_gene_variant | MODIFIER | c.-361C>T| |
S203 |
6 | BAA10g20210 | A10 | 18277985 | G | A | missense_variant&splice_region_variant | MODERATE | c.389G>A|p.Arg130Lys |
S263 |
7 | BAA10g20210 | A10 | 18278085 | G | A | missense_variant | MODERATE | c.395G>A|p.Cys132Tyr |
S167 |
8 | BAA10g20210 | A10 | 18278576 | C | T | missense_variant | MODERATE | c.683C>T|p.Thr228Ile |
S13 |
9 | BAA10g20210 | A10 | 18279428 | C | T | missense_variant | MODERATE | c.1156C>T|p.Leu386Phe |
S289 S79 S91 |