Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41450 | A05 | 39605782 | G | A | upstream_gene_variant | MODIFIER | c.-3102G>A| |
S202 |
2 | BAA05g41450 | A05 | 39608727 | C | T | upstream_gene_variant | MODIFIER | c.-157C>T| |
S33 |
3 | BAA05g41450 | A05 | 39609011 | C | T | missense_variant | MODERATE | c.128C>T|p.Ser43Phe |
S186 S301 |
4 | BAA05g41450 | A05 | 39609082 | G | A | missense_variant | MODERATE | c.199G>A|p.Glu67Lys |
S81 |
5 | BAA05g41450 | A05 | 39609088 | G | A | missense_variant | MODERATE | c.205G>A|p.Gly69Arg |
S80 |
6 | BAA05g41450 | A05 | 39609340 | G | A | missense_variant | MODERATE | c.343G>A|p.Glu115Lys |
S138 |
7 | BAA05g41450 | A05 | 39609627 | A | C | missense_variant | MODERATE | c.416A>C|p.Gln139Pro |
S138 S144 S191 S201 |
8 | BAA05g41450 | A05 | 39611134 | C | T | synonymous_variant | LOW | c.1261C>T|p.Leu421Leu |
S282 |
9 | BAA05g41450 | A05 | 39611404 | G | A | missense_variant | MODERATE | c.1450G>A|p.Asp484Asn |
S278 |
10 | BAA05g41450 | A05 | 39611462 | G | A | missense_variant | MODERATE | c.1508G>A|p.Gly503Glu |
S223 |