Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g25160 | A08 | 18222666 | G | A | missense_variant | MODERATE | c.4G>A|p.Glu2Lys |
S292 |
2 | BAA08g25160 | A08 | 18223980 | G | A | stop_gained | HIGH | c.504G>A|p.Trp168* |
S130 |
3 | BAA08g25160 | A08 | 18224888 | C | T | missense_variant | MODERATE | c.1412C>T|p.Ala471Val |
S114 |
4 | BAA08g25160 | A08 | 18224956 | C | T | missense_variant | MODERATE | c.1480C>T|p.Pro494Ser |
S35 |
5 | BAA08g25160 | A08 | 18225167 | G | A | missense_variant | MODERATE | c.1691G>A|p.Arg564Lys |
S130 |
6 | BAA08g25160 | A08 | 18225841 | C | T | missense_variant | MODERATE | c.2215C>T|p.His739Tyr |
S78 |
7 | BAA08g25160 | A08 | 18226696 | C | T | splice_region_variant&intron_variant | LOW | c.2805+6C>T| |
S293 |
8 | BAA08g25160 | A08 | 18226841 | C | T | synonymous_variant | LOW | c.2871C>T|p.Asn957Asn |
S201 |
9 | BAA08g25160 | A08 | 18228085 | C | T | downstream_gene_variant | MODIFIER | c.*1061C>T| |
S6 |