Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 14 of 14 records


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