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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g19060 A02 9871212 G A downstream_gene_variant MODIFIER c.*4263C>T| S296
2 BAA02g19060 A02 9876222 C T missense_variant MODERATE c.857G>A|p.Gly286Glu S275
3 BAA02g19060 A02 9877062 C T synonymous_variant LOW c.252G>A|p.Glu84Glu S177
4 BAA02g19060 A02 9879000 C T upstream_gene_variant MODIFIER c.-1305G>A| S270
5 BAA02g19060 A02 9879183 G A upstream_gene_variant MODIFIER c.-1488C>T| S76
6 BAA02g19060 A02 9879251 G A upstream_gene_variant MODIFIER c.-1556C>T| S34
7 BAA02g19060 A02 9879360 G A upstream_gene_variant MODIFIER c.-1665C>T| S231
8 BAA02g19060 A02 9879489 G A upstream_gene_variant MODIFIER c.-1794C>T| S282
9 BAA02g19060 A02 9879812 G A upstream_gene_variant MODIFIER c.-2117C>T| S125
10 BAA02g19060 A02 9880168 G A upstream_gene_variant MODIFIER c.-2473C>T| S50
11 BAA02g19060 A02 9880503 G A upstream_gene_variant MODIFIER c.-2808C>T| S153
S213
12 BAA02g19060 A02 9880823 G A upstream_gene_variant MODIFIER c.-3128C>T| S34
13 BAA02g19060 A02 9880884 G A upstream_gene_variant MODIFIER c.-3189C>T| S296
14 BAA02g19060 A02 9881622 G A upstream_gene_variant MODIFIER c.-3927C>T| S41
15 BAA02g19060 A02 9881754 G A upstream_gene_variant MODIFIER c.-4059C>T| S295