Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26240 | A10 | 20889123 | C | T | missense_variant | MODERATE | c.439G>A|p.Ala147Thr |
S115 |
2 | BAA10g26240 | A10 | 20889155 | C | T | missense_variant | MODERATE | c.407G>A|p.Arg136Gln |
S115 |
3 | BAA10g26240 | A10 | 20889204 | G | A | missense_variant | MODERATE | c.358C>T|p.Pro120Ser |
S179 |
4 | BAA10g26240 | A10 | 20889574 | C | T | missense_variant | MODERATE | c.157G>A|p.Gly53Arg |
S46 |
5 | BAA10g26240 | A10 | 20890136 | C | T | upstream_gene_variant | MODIFIER | c.-406G>A| |
S174 S216 S241 S27 |
6 | BAA10g26240 | A10 | 20890179 | G | A | upstream_gene_variant | MODIFIER | c.-449C>T| |
S279 |
7 | BAA10g26240 | A10 | 20891214 | C | T | upstream_gene_variant | MODIFIER | c.-1484G>A| |
S295 |
8 | BAA10g26240 | A10 | 20891553 | C | T | upstream_gene_variant | MODIFIER | c.-1823G>A| |
S204 |
9 | BAA10g26240 | A10 | 20893497 | G | A | upstream_gene_variant | MODIFIER | c.-3767C>T| |
S245 |