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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g32340 A09 40971495 C T missense_variant MODERATE c.2989G>A|p.Asp997Asn S133
2 BAA09g32340 A09 40971555 G A missense_variant MODERATE c.2929C>T|p.His977Tyr S71
3 BAA09g32340 A09 40972227 G A splice_region_variant&intron_variant LOW c.2371-8C>T| S59
4 BAA09g32340 A09 40972870 G A synonymous_variant LOW c.2136C>T|p.Ser712Ser S4
5 BAA09g32340 A09 40974459 C T synonymous_variant LOW c.888G>A|p.Lys296Lys S153
6 BAA09g32340 A09 40975193 C T missense_variant MODERATE c.346G>A|p.Asp116Asn S23
7 BAA09g32340 A09 40978947 C T upstream_gene_variant MODIFIER c.-3254G>A| S303
8 BAA09g32340 A09 40979109 G A upstream_gene_variant MODIFIER c.-3416C>T| S132
S137
S215
9 BAA09g32340 A09 40979348 C T upstream_gene_variant MODIFIER c.-3655G>A| S143
10 BAA09g32340 A09 40979573 C T upstream_gene_variant MODIFIER c.-3880G>A| S30
S31
11 BAA09g32340 A09 40979982 C T upstream_gene_variant MODIFIER c.-4289G>A| S247
12 BAA09g32340 A09 40980194 C T upstream_gene_variant MODIFIER c.-4501G>A| S146
13 BAA09g32340 A09 40980612 T C upstream_gene_variant MODIFIER c.-4919A>G| S172
S217