Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08130 | A10 | 5548832 | G | A | upstream_gene_variant | MODIFIER | c.-1873G>A| |
S278 |
2 | BAA10g08130 | A10 | 5549044 | C | T | upstream_gene_variant | MODIFIER | c.-1661C>T| |
S95 |
3 | BAA10g08130 | A10 | 5549075 | G | A | upstream_gene_variant | MODIFIER | c.-1630G>A| |
S296 |
4 | BAA10g08130 | A10 | 5550212 | G | A | upstream_gene_variant | MODIFIER | c.-493G>A| |
S107 |
5 | BAA10g08130 | A10 | 5550539 | C | T | upstream_gene_variant | MODIFIER | c.-166C>T| |
S132 S137 S89 |
6 | BAA10g08130 | A10 | 5550608 | G | A | upstream_gene_variant | MODIFIER | c.-97G>A| |
S11 |
7 | BAA10g08130 | A10 | 5550785 | G | A | synonymous_variant | LOW | c.81G>A|p.Arg27Arg |
S174 S216 S241 S265 S27 S39 |
8 | BAA10g08130 | A10 | 5552921 | C | T | missense_variant | MODERATE | c.1220C>T|p.Pro407Leu |
S181 S199 |
9 | BAA10g08130 | A10 | 5555197 | C | T | downstream_gene_variant | MODIFIER | c.*2013C>T| |
S166 |