Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g26210 | A03 | 12027754 | C | T | missense_variant | MODERATE | c.2689G>A|p.Ala897Thr |
S179 |
2 | BAA03g26210 | A03 | 12028650 | G | A | missense_variant | MODERATE | c.2189C>T|p.Ala730Val |
S95 |
3 | BAA03g26210 | A03 | 12028660 | C | T | missense_variant | MODERATE | c.2179G>A|p.Asp727Asn |
S152 |
4 | BAA03g26210 | A03 | 12028797 | C | T | missense_variant | MODERATE | c.2042G>A|p.Arg681Lys |
S44 |
5 | BAA03g26210 | A03 | 12029210 | C | T | missense_variant | MODERATE | c.1738G>A|p.Asp580Asn |
S59 |
6 | BAA03g26210 | A03 | 12029578 | G | A | missense_variant | MODERATE | c.1370C>T|p.Ser457Phe |
S47 |
7 | BAA03g26210 | A03 | 12031979 | C | T | splice_region_variant&intron_variant | LOW | c.646-5G>A| |
S224 |
8 | BAA03g26210 | A03 | 12034011 | C | T | upstream_gene_variant | MODIFIER | c.-935G>A| |
S158 |
9 | BAA03g26210 | A03 | 12034671 | C | T | upstream_gene_variant | MODIFIER | c.-1595G>A| |
S125 |
10 | BAA03g26210 | A03 | 12037798 | C | T | upstream_gene_variant | MODIFIER | c.-4722G>A| |
S115 |