Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18080 | A10 | 17099747 | G | A | upstream_gene_variant | MODIFIER | c.-4911G>A| |
S262 |
2 | BAA10g18080 | A10 | 17100158 | G | A | upstream_gene_variant | MODIFIER | c.-4500G>A| |
S182 |
3 | BAA10g18080 | A10 | 17100427 | C | T | upstream_gene_variant | MODIFIER | c.-4231C>T| |
S86 |
4 | BAA10g18080 | A10 | 17101125 | C | T | upstream_gene_variant | MODIFIER | c.-3533C>T| |
S162 |
5 | BAA10g18080 | A10 | 17102566 | G | A | upstream_gene_variant | MODIFIER | c.-2092G>A| |
S128 |
6 | BAA10g18080 | A10 | 17103046 | C | T | upstream_gene_variant | MODIFIER | c.-1612C>T| |
S203 |
7 | BAA10g18080 | A10 | 17103556 | G | A | upstream_gene_variant | MODIFIER | c.-1102G>A| |
S295 |
8 | BAA10g18080 | A10 | 17103799 | C | T | upstream_gene_variant | MODIFIER | c.-859C>T| |
S23 |
9 | BAA10g18080 | A10 | 17105819 | C | T | missense_variant | MODERATE | c.1162C>T|p.Pro388Ser |
S174 S27 S39 |
10 | BAA10g18080 | A10 | 17106812 | G | A | missense_variant | MODERATE | c.2155G>A|p.Asp719Asn |
S32 |
11 | BAA10g18080 | A10 | 17106857 | C | T | synonymous_variant | LOW | c.2200C>T|p.Leu734Leu |
S6 |