Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05490 | A08 | 4169646 | C | T | missense_variant | MODERATE | c.1186G>A|p.Gly396Arg |
S134 |
2 | BAA08g05490 | A08 | 4169826 | C | T | missense_variant | MODERATE | c.1076G>A|p.Gly359Glu |
S66 |
3 | BAA08g05490 | A08 | 4170306 | G | T | missense_variant | MODERATE | c.686C>A|p.Pro229Gln |
S250 |
4 | BAA08g05490 | A08 | 4170326 | G | A | synonymous_variant | LOW | c.666C>T|p.Ser222Ser |
S297 |
5 | BAA08g05490 | A08 | 4171356 | C | T | upstream_gene_variant | MODIFIER | c.-85G>A| |
S245 |
6 | BAA08g05490 | A08 | 4172458 | C | T | upstream_gene_variant | MODIFIER | c.-1187G>A| |
S120 |
7 | BAA08g05490 | A08 | 4172623 | C | T | upstream_gene_variant | MODIFIER | c.-1352G>A| |
S173 |
8 | BAA08g05490 | A08 | 4174992 | C | T | upstream_gene_variant | MODIFIER | c.-3721G>A| |
S251 |
9 | BAA08g05490 | A08 | 4175108 | G | A | upstream_gene_variant | MODIFIER | c.-3837C>T| |
S178 |