Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g04220 | A05 | 2047120 | C | T | missense_variant | MODERATE | c.1403G>A|p.Gly468Asp |
S267 |
2 | BAA05g04220 | A05 | 2047304 | C | T | missense_variant | MODERATE | c.1219G>A|p.Glu407Lys |
S110 |
3 | BAA05g04220 | A05 | 2047337 | C | T | missense_variant | MODERATE | c.1186G>A|p.Val396Met |
S109 |
4 | BAA05g04220 | A05 | 2047700 | C | T | missense_variant | MODERATE | c.823G>A|p.Glu275Lys |
S236 |
5 | BAA05g04220 | A05 | 2048090 | C | T | missense_variant | MODERATE | c.433G>A|p.Glu145Lys |
S71 |
6 | BAA05g04220 | A05 | 2048145 | G | A | synonymous_variant | LOW | c.378C>T|p.Leu126Leu |
S157 S163 |
7 | BAA05g04220 | A05 | 2048254 | G | A | missense_variant | MODERATE | c.269C>T|p.Thr90Ile |
S244 |
8 | BAA05g04220 | A05 | 2048319 | G | A | synonymous_variant | LOW | c.204C>T|p.Val68Val |
S190 |
9 | BAA05g04220 | A05 | 2048425 | G | A | missense_variant | MODERATE | c.98C>T|p.Ser33Phe |
S241 |
10 | BAA05g04220 | A05 | 2048727 | C | T | upstream_gene_variant | MODIFIER | c.-205G>A| |
S15 S3 |
11 | BAA05g04220 | A05 | 2048899 | C | T | upstream_gene_variant | MODIFIER | c.-377G>A| |
S237 |
12 | BAA05g04220 | A05 | 2048941 | C | T | upstream_gene_variant | MODIFIER | c.-419G>A| |
S135 |