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 BAA02g44190 A02 36469796 G A synonymous_variant LOW c.897C>T|p.Pro299Pro S207
2 BAA02g44190 A02 36470673 C T missense_variant MODERATE c.685G>A|p.Gly229Ser S92
3 BAA02g44190 A02 36470859 C T missense_variant MODERATE c.499G>A|p.Glu167Lys S116
4 BAA02g44190 A02 36472868 C T intron_variant MODIFIER c.447-1957G>A| S133
S275
5 BAA02g44190 A02 36474328 C T intron_variant MODIFIER c.446+778G>A| S299
6 BAA02g44190 A02 36474477 G A intron_variant MODIFIER c.446+629C>T| S217
S248
7 BAA02g44190 A02 36474574 C T intron_variant MODIFIER c.446+532G>A| S72
S78
8 BAA02g44190 A02 36474784 C T intron_variant MODIFIER c.446+322G>A| S3
9 BAA02g44190 A02 36475874 C T intron_variant MODIFIER c.199-521G>A| S23
10 BAA02g44190 A02 36477166 C T upstream_gene_variant MODIFIER c.-513G>A| S172
S217
11 BAA02g44190 A02 36477582 C T upstream_gene_variant MODIFIER c.-929G>A| S131
12 BAA02g44190 A02 36478019 A T upstream_gene_variant MODIFIER c.-1366T>A| S35
13 BAA02g44190 A02 36478234 G A upstream_gene_variant MODIFIER c.-1581C>T| S246
14 BAA02g44190 A02 36480285 C T upstream_gene_variant MODIFIER c.-3632G>A| S17
15 BAA02g44190 A02 36480887 A T upstream_gene_variant MODIFIER c.-4234T>A| S123