Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g23290 | A05 | 27977744 | G | A | missense_variant | MODERATE | c.88G>A|p.Val30Ile |
S276 |
2 | BAA05g23290 | A05 | 27977874 | C | T | missense_variant | MODERATE | c.218C>T|p.Ser73Leu |
S191 |
3 | BAA05g23290 | A05 | 27978695 | G | A | splice_region_variant&synonymous_variant | LOW | c.798G>A|p.Glu266Glu |
S212 |
4 | BAA05g23290 | A05 | 27978820 | G | A | missense_variant | MODERATE | c.847G>A|p.Gly283Ser |
S129 |
5 | BAA05g23290 | A05 | 27979201 | C | T | synonymous_variant | LOW | c.1032C>T|p.Ile344Ile |
S67 |
6 | BAA05g23290 | A05 | 27979563 | G | A | intron_variant | MODIFIER | c.1092-109G>A| |
S217 S248 |
7 | BAA05g23290 | A05 | 27979570 | G | A | intron_variant | MODIFIER | c.1092-102G>A| |
S125 |
8 | BAA05g23290 | A05 | 27979799 | C | T | intron_variant | MODIFIER | c.1209+10C>T| |
S99 |
9 | BAA05g23290 | A05 | 27979824 | G | A | intron_variant | MODIFIER | c.1209+35G>A| |
S144 |
10 | BAA05g23290 | A05 | 27980045 | G | A | missense_variant | MODERATE | c.1346G>A|p.Ser449Asn |
S34 |
11 | BAA05g23290 | A05 | 27981426 | G | A | missense_variant | MODERATE | c.2327G>A|p.Arg776Lys |
S252 |
12 | BAA05g23290 | A05 | 27981793 | C | T | intron_variant | MODIFIER | c.2584-10C>T| |
S288 |
13 | BAA05g23290 | A05 | 27981903 | G | A | missense_variant | MODERATE | c.2684G>A|p.Gly895Asp |
S122 |
14 | BAA05g23290 | A05 | 27990602 | C | T | downstream_gene_variant | MODIFIER | c.*4667C>T| |
S47 |
15 | BAA05g23290 | A05 | 27990747 | G | A | downstream_gene_variant | MODIFIER | c.*4812G>A| |
S9 |