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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g17090 A10 16612275 G A downstream_gene_variant MODIFIER c.*2023C>T| S9
2 BAA10g17090 A10 16612453 C T downstream_gene_variant MODIFIER c.*1845G>A| S95
3 BAA10g17090 A10 16612559 T A downstream_gene_variant MODIFIER c.*1739A>T| S92
4 BAA10g17090 A10 16612974 C T downstream_gene_variant MODIFIER c.*1324G>A| S225
S73
5 BAA10g17090 A10 16613283 C T downstream_gene_variant MODIFIER c.*1015G>A| S153
S213
6 BAA10g17090 A10 16613408 G A downstream_gene_variant MODIFIER c.*890C>T| S241
7 BAA10g17090 A10 16613460 C T downstream_gene_variant MODIFIER c.*838G>A| S42
8 BAA10g17090 A10 16613533 G A downstream_gene_variant MODIFIER c.*765C>T| S245
9 BAA10g17090 A10 16613643 G A downstream_gene_variant MODIFIER c.*655C>T| S4
10 BAA10g17090 A10 16613761 C T downstream_gene_variant MODIFIER c.*537G>A| S18
11 BAA10g17090 A10 16614059 C T downstream_gene_variant MODIFIER c.*239G>A| S180
12 BAA10g17090 A10 16614380 T A missense_variant MODERATE c.956A>T|p.Asn319Ile S208
S219
13 BAA10g17090 A10 16616680 G A missense_variant MODERATE c.386C>T|p.Ser129Phe S284
14 BAA10g17090 A10 16616707 C T missense_variant MODERATE c.359G>A|p.Gly120Glu S144
15 BAA10g17090 A10 16616769 C T synonymous_variant LOW c.297G>A|p.Glu99Glu S204
16 BAA10g17090 A10 16616816 C T missense_variant MODERATE c.250G>A|p.Glu84Lys S301
S304
17 BAA10g17090 A10 16617010 G A missense_variant MODERATE c.56C>T|p.Thr19Ile S74
18 BAA10g17090 A10 16618602 G A upstream_gene_variant MODIFIER c.-1537C>T| S182
19 BAA10g17090 A10 16619599 C T upstream_gene_variant MODIFIER c.-2534G>A| S56
20 BAA10g17090 A10 16619743 T A upstream_gene_variant MODIFIER c.-2678A>T| S291