Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04600 | A10 | 2343133 | C | T | missense_variant | MODERATE | c.52C>T|p.Arg18Cys |
S6 |
2 | BAA10g04600 | A10 | 2343842 | C | T | missense_variant | MODERATE | c.460C>T|p.Leu154Phe |
S270 |
3 | BAA10g04600 | A10 | 2344084 | G | A | synonymous_variant | LOW | c.702G>A|p.Glu234Glu |
S186 |
4 | BAA10g04600 | A10 | 2344253 | G | A | missense_variant | MODERATE | c.871G>A|p.Gly291Arg |
S19 |
5 | BAA10g04600 | A10 | 2344349 | G | A | missense_variant | MODERATE | c.967G>A|p.Glu323Lys |
S255 |
6 | BAA10g04600 | A10 | 2344484 | G | A | missense_variant | MODERATE | c.1021G>A|p.Asp341Asn |
S84 S93 |
7 | BAA10g04600 | A10 | 2344491 | C | T | missense_variant | MODERATE | c.1028C>T|p.Ser343Phe |
S181 |
8 | BAA10g04600 | A10 | 2346076 | G | A | missense_variant | MODERATE | c.1546G>A|p.Asp516Asn |
|
9 | BAA10g04600 | A10 | 2347349 | G | A | missense_variant | MODERATE | c.2384G>A|p.Arg795Lys |
S25 |
10 | BAA10g04600 | A10 | 2348969 | G | A | missense_variant | MODERATE | c.3433G>A|p.Glu1145Lys |
S111 |
11 | BAA10g04600 | A10 | 2349237 | C | T | downstream_gene_variant | MODIFIER | c.*155C>T| |
S282 |
12 | BAA10g04600 | A10 | 2349363 | G | A | downstream_gene_variant | MODIFIER | c.*281G>A| |
S17 |
13 | BAA10g04600 | A10 | 2350453 | C | T | downstream_gene_variant | MODIFIER | c.*1371C>T| |
S208 S93 |