Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19220 | A08 | 15207229 | C | T | upstream_gene_variant | MODIFIER | c.-1272C>T| |
S167 |
2 | BAA08g19220 | A08 | 15207408 | C | T | upstream_gene_variant | MODIFIER | c.-1093C>T| |
S184 |
3 | BAA08g19220 | A08 | 15207574 | C | T | upstream_gene_variant | MODIFIER | c.-927C>T| |
S57 |
4 | BAA08g19220 | A08 | 15207640 | C | T | upstream_gene_variant | MODIFIER | c.-861C>T| |
S189 |
5 | BAA08g19220 | A08 | 15209277 | C | T | synonymous_variant | LOW | c.352C>T|p.Leu118Leu |
S244 |
6 | BAA08g19220 | A08 | 15209682 | C | T | missense_variant | MODERATE | c.529C>T|p.Leu177Phe |
S250 |
7 | BAA08g19220 | A08 | 15209933 | C | T | synonymous_variant | LOW | c.618C>T|p.Pro206Pro |
S169 |
8 | BAA08g19220 | A08 | 15212018 | C | T | synonymous_variant | LOW | c.1831C>T|p.Leu611Leu |
S186 |
9 | BAA08g19220 | A08 | 15212346 | C | T | missense_variant | MODERATE | c.2068C>T|p.His690Tyr |
S88 |
10 | BAA08g19220 | A08 | 15212368 | C | T | missense_variant | MODERATE | c.2090C>T|p.Ala697Val |
S247 |
11 | BAA08g19220 | A08 | 15213297 | C | T | missense_variant | MODERATE | c.2590C>T|p.Pro864Ser |
S265 |
12 | BAA08g19220 | A08 | 15213315 | G | A | missense_variant | MODERATE | c.2608G>A|p.Glu870Lys |
S150 |