Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23770 | A08 | 17521326 | G | A | missense_variant | MODERATE | c.2126C>T|p.Thr709Ile |
S265 |
2 | BAA08g23770 | A08 | 17521404 | C | T | missense_variant | MODERATE | c.2048G>A|p.Arg683Lys |
S133 |
3 | BAA08g23770 | A08 | 17522185 | C | T | missense_variant | MODERATE | c.1267G>A|p.Asp423Asn |
S1 S90 |
4 | BAA08g23770 | A08 | 17522568 | C | T | stop_gained | HIGH | c.884G>A|p.Trp295* |
S187 |
5 | BAA08g23770 | A08 | 17522774 | G | A | synonymous_variant | LOW | c.678C>T|p.Ala226Ala |
S175 |
6 | BAA08g23770 | A08 | 17523330 | G | A | missense_variant | MODERATE | c.122C>T|p.Ala41Val |
S61 |
7 | BAA08g23770 | A08 | 17523722 | G | A | upstream_gene_variant | MODIFIER | c.-83C>T| |
S62 |
8 | BAA08g23770 | A08 | 17523897 | G | A | upstream_gene_variant | MODIFIER | c.-258C>T| |
S282 |
9 | BAA08g23770 | A08 | 17527387 | G | A | upstream_gene_variant | MODIFIER | c.-3748C>T| |
S139 |
10 | BAA08g23770 | A08 | 17527614 | G | A | upstream_gene_variant | MODIFIER | c.-3975C>T| |
S37 |
11 | BAA08g23770 | A08 | 17528007 | C | T | upstream_gene_variant | MODIFIER | c.-4368G>A| |
S60 |