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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g10100 A02 4456794 C T upstream_gene_variant MODIFIER c.-4702C>T| S25
2 BAA02g10100 A02 4456822 C T upstream_gene_variant MODIFIER c.-4674C>T| S6
3 BAA02g10100 A02 4459134 G A upstream_gene_variant MODIFIER c.-2362G>A| S84
S93
4 BAA02g10100 A02 4461498 G A start_lost HIGH c.3G>A|p.Met1? S37
5 BAA02g10100 A02 4461612 C T synonymous_variant LOW c.117C>T|p.Cys39Cys S179
6 BAA02g10100 A02 4461703 G A missense_variant MODERATE c.208G>A|p.Asp70Asn S188
7 BAA02g10100 A02 4463437 G A missense_variant MODERATE c.1208G>A|p.Gly403Glu S131
8 BAA02g10100 A02 4463564 G A intron_variant MODIFIER c.1244+91G>A| S282
9 BAA02g10100 A02 4463615 G A intron_variant MODIFIER c.1244+142G>A| S187
10 BAA02g10100 A02 4463787 C T intron_variant MODIFIER c.1244+314C>T| S234
11 BAA02g10100 A02 4464432 G A intron_variant MODIFIER c.1245-13G>A| S247
12 BAA02g10100 A02 4464715 C T synonymous_variant LOW c.1515C>T|p.Ile505Ile S32
13 BAA02g10100 A02 4467322 G A downstream_gene_variant MODIFIER c.*2568G>A| S166
14 BAA02g10100 A02 4468787 C T downstream_gene_variant MODIFIER c.*4033C>T| S272
15 BAA02g10100 A02 4469103 C T downstream_gene_variant MODIFIER c.*4349C>T| S180
16 BAA02g10100 A02 4469617 C T downstream_gene_variant MODIFIER c.*4863C>T| S305