Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13490 | A05 | 6993739 | G | A | synonymous_variant | LOW | c.51G>A|p.Leu17Leu |
S108 |
2 | BAA05g13490 | A05 | 6993803 | G | A | missense_variant | MODERATE | c.115G>A|p.Asp39Asn |
S294 |
3 | BAA05g13490 | A05 | 6993863 | C | T | missense_variant | MODERATE | c.175C>T|p.Leu59Phe |
S289 S290 |
4 | BAA05g13490 | A05 | 6993898 | G | A | synonymous_variant | LOW | c.210G>A|p.Gln70Gln |
S34 |
5 | BAA05g13490 | A05 | 6994194 | G | A | missense_variant | MODERATE | c.415G>A|p.Asp139Asn |
S134 |
6 | BAA05g13490 | A05 | 6994648 | C | T | stop_gained&splice_region_variant | HIGH | c.724C>T|p.Gln242* |
S135 S39 |
7 | BAA05g13490 | A05 | 6994974 | C | T | splice_region_variant&intron_variant | LOW | c.975+5C>T| |
S251 |
8 | BAA05g13490 | A05 | 6995080 | C | T | missense_variant | MODERATE | c.979C>T|p.Arg327Cys |
S25 |
9 | BAA05g13490 | A05 | 6995734 | C | T | missense_variant | MODERATE | c.1229C>T|p.Ser410Phe |
S292 |
10 | BAA05g13490 | A05 | 6995973 | C | T | stop_gained | HIGH | c.1468C>T|p.Gln490* |
S53 |
11 | BAA05g13490 | A05 | 6996061 | G | A | missense_variant | MODERATE | c.1480G>A|p.Gly494Arg |
S32 |
12 | BAA05g13490 | A05 | 6996078 | C | T | synonymous_variant | LOW | c.1497C>T|p.Val499Val |
S135 |
13 | BAA05g13490 | A05 | 6996164 | C | T | missense_variant | MODERATE | c.1583C>T|p.Ser528Leu |
S87 |