Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22640 | A08 | 16950990 | C | T | upstream_gene_variant | MODIFIER | c.-4789C>T| |
S230 |
2 | BAA08g22640 | A08 | 16952747 | G | A | upstream_gene_variant | MODIFIER | c.-3032G>A| |
S13 |
3 | BAA08g22640 | A08 | 16955829 | G | A | stop_gained | HIGH | c.51G>A|p.Trp17* |
S174 S39 |
4 | BAA08g22640 | A08 | 16956731 | C | T | missense_variant | MODERATE | c.953C>T|p.Ser318Phe |
S169 |
5 | BAA08g22640 | A08 | 16957026 | C | T | missense_variant | MODERATE | c.1168C>T|p.Pro390Ser |
S276 |
6 | BAA08g22640 | A08 | 16957059 | C | T | missense_variant | MODERATE | c.1201C>T|p.Arg401Cys |
S157 S163 |
7 | BAA08g22640 | A08 | 16957287 | G | A | missense_variant | MODERATE | c.1346G>A|p.Gly449Glu |
S140 |
8 | BAA08g22640 | A08 | 16957442 | C | T | missense_variant | MODERATE | c.1424C>T|p.Ala475Val |
S18 |
9 | BAA08g22640 | A08 | 16957522 | G | A | missense_variant | MODERATE | c.1504G>A|p.Glu502Lys |
S265 |
10 | BAA08g22640 | A08 | 16957555 | G | A | missense_variant | MODERATE | c.1537G>A|p.Ala513Thr |
S221 |