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 BAA04g10500 A04 16618799 G A intron_variant MODIFIER c.134+1191G>A| S149
2 BAA04g10500 A04 16619079 C T intron_variant MODIFIER c.135-1120C>T| S249
3 BAA04g10500 A04 16619355 G A intron_variant MODIFIER c.135-844G>A| S19
4 BAA04g10500 A04 16620471 C T intron_variant MODIFIER c.368+39C>T| S185
5 BAA04g10500 A04 16621997 C T intron_variant MODIFIER c.446+32C>T| S240
6 BAA04g10500 A04 16628409 G A missense_variant MODERATE c.793G>A|p.Glu265Lys S38
7 BAA04g10500 A04 16629139 C T downstream_gene_variant MODIFIER c.*686C>T| S32
8 BAA04g10500 A04 16631404 G A downstream_gene_variant MODIFIER c.*2951G>A| S256
9 BAA04g10500 A04 16631812 C A downstream_gene_variant MODIFIER c.*3359C>A| S46
10 BAA04g10500 A04 16631844 G A downstream_gene_variant MODIFIER c.*3391G>A| S192
11 BAA04g10500 A04 16632436 G A downstream_gene_variant MODIFIER c.*3983G>A| S47
12 BAA04g10500 A04 16632810 C T downstream_gene_variant MODIFIER c.*4357C>T| S111
13 BAA04g10500 A04 16633255 C T downstream_gene_variant MODIFIER c.*4802C>T| S170
14 BAA04g10500 A04 16633410 C T downstream_gene_variant MODIFIER c.*4957C>T| S204