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 BAA02g45410 A02 37183313 G A missense_variant MODERATE c.388G>A|p.Glu130Lys S80
2 BAA02g45410 A02 37183606 G A missense_variant MODERATE c.524G>A|p.Gly175Asp S111
3 BAA02g45410 A02 37183658 C T synonymous_variant LOW c.576C>T|p.Val192Val S3
4 BAA02g45410 A02 37183831 C T missense_variant MODERATE c.674C>T|p.Ser225Phe S171
5 BAA02g45410 A02 37183920 C T stop_gained HIGH c.763C>T|p.Gln255* S135
6 BAA02g45410 A02 37184136 C T synonymous_variant LOW c.897C>T|p.Phe299Phe S64
7 BAA02g45410 A02 37184705 G A missense_variant MODERATE c.1202G>A|p.Gly401Glu S5
8 BAA02g45410 A02 37185322 G A missense_variant MODERATE c.1756G>A|p.Gly586Arg S240
9 BAA02g45410 A02 37185984 G A missense_variant MODERATE c.2188G>A|p.Glu730Lys S269
10 BAA02g45410 A02 37186077 G A missense_variant MODERATE c.2281G>A|p.Asp761Asn S293
11 BAA02g45410 A02 37190240 C T downstream_gene_variant MODIFIER c.*574C>T| S303
12 BAA02g45410 A02 37192674 C T downstream_gene_variant MODIFIER c.*3008C>T| S112
13 BAA02g45410 A02 37192756 C T downstream_gene_variant MODIFIER c.*3090C>T| S190
14 BAA02g45410 A02 37192962 C T downstream_gene_variant MODIFIER c.*3296C>T| S59