Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g43690 | A03 | 20709721 | G | A | missense_variant | MODERATE | c.2869C>T|p.Leu957Phe |
S233 |
2 | BAA03g43690 | A03 | 20709736 | C | T | missense_variant | MODERATE | c.2854G>A|p.Val952Met |
S86 |
3 | BAA03g43690 | A03 | 20711938 | C | T | stop_gained | HIGH | c.1503G>A|p.Trp501* |
S139 |
4 | BAA03g43690 | A03 | 20712129 | C | T | missense_variant | MODERATE | c.1396G>A|p.Glu466Lys |
S295 |
5 | BAA03g43690 | A03 | 20712191 | G | A | missense_variant | MODERATE | c.1334C>T|p.Thr445Ile |
S297 |
6 | BAA03g43690 | A03 | 20713885 | G | A | missense_variant | MODERATE | c.484C>T|p.Leu162Phe |
S286 |
7 | BAA03g43690 | A03 | 20714035 | G | A | missense_variant | MODERATE | c.334C>T|p.Arg112Cys |
S213 |
8 | BAA03g43690 | A03 | 20714219 | C | T | missense_variant | MODERATE | c.230G>A|p.Arg77Lys |
S75 S81 |
9 | BAA03g43690 | A03 | 20715002 | C | T | upstream_gene_variant | MODIFIER | c.-554G>A| |
S275 |
10 | BAA03g43690 | A03 | 20715498 | C | T | upstream_gene_variant | MODIFIER | c.-1050G>A| |
S38 |
11 | BAA03g43690 | A03 | 20715769 | C | T | upstream_gene_variant | MODIFIER | c.-1321G>A| |
S301 S304 |
12 | BAA03g43690 | A03 | 20715925 | G | A | upstream_gene_variant | MODIFIER | c.-1477C>T| |
S294 |
13 | BAA03g43690 | A03 | 20716605 | T | A | upstream_gene_variant | MODIFIER | c.-2157A>T| |
S284 |
14 | BAA03g43690 | A03 | 20716988 | C | T | upstream_gene_variant | MODIFIER | c.-2540G>A| |
S242 |
15 | BAA03g43690 | A03 | 20718084 | G | A | upstream_gene_variant | MODIFIER | c.-3636C>T| |
S272 |