Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38780 | A05 | 38024667 | G | A | synonymous_variant | LOW | c.30G>A|p.Arg10Arg |
S96 |
2 | BAA05g38780 | A05 | 38024741 | G | A | missense_variant | MODERATE | c.104G>A|p.Ser35Asn |
S79 S84 |
3 | BAA05g38780 | A05 | 38024780 | G | A | missense_variant | MODERATE | c.143G>A|p.Arg48Lys |
S251 |
4 | BAA05g38780 | A05 | 38026547 | G | A | missense_variant | MODERATE | c.1013G>A|p.Arg338Lys |
S6 |
5 | BAA05g38780 | A05 | 38029365 | C | T | synonymous_variant | LOW | c.2040C>T|p.Phe680Phe |
S189 |
6 | BAA05g38780 | A05 | 38029748 | G | A | missense_variant | MODERATE | c.2087G>A|p.Arg696Lys |
S34 |
7 | BAA05g38780 | A05 | 38031325 | G | A | missense_variant | MODERATE | c.2581G>A|p.Glu861Lys |
S107 |
8 | BAA05g38780 | A05 | 38032391 | C | T | intron_variant | MODIFIER | c.3194+17C>T| |
S140 |
9 | BAA05g38780 | A05 | 38033702 | C | T | synonymous_variant | LOW | c.3828C>T|p.Asp1276Asp |
S208 S93 |
10 | BAA05g38780 | A05 | 38034773 | C | T | missense_variant | MODERATE | c.4315C>T|p.Leu1439Phe |
S261 |
11 | BAA05g38780 | A05 | 38034851 | C | T | missense_variant | MODERATE | c.4393C>T|p.Leu1465Phe |
S110 |
12 | BAA05g38780 | A05 | 38035482 | G | A | synonymous_variant | LOW | c.4656G>A|p.Leu1552Leu |
S281 |
13 | BAA05g38780 | A05 | 38036099 | C | T | missense_variant | MODERATE | c.4909C>T|p.Leu1637Phe |
S162 |
14 | BAA05g38780 | A05 | 38036352 | G | A | missense_variant | MODERATE | c.5084G>A|p.Gly1695Asp |
S6 |