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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g29370 A05 32873195 C T downstream_gene_variant MODIFIER c.*4698G>A| S268
2 BAA05g29370 A05 32873821 G A downstream_gene_variant MODIFIER c.*4072C>T| S156
3 BAA05g29370 A05 32874467 G A downstream_gene_variant MODIFIER c.*3426C>T| S84
4 BAA05g29370 A05 32874511 G A downstream_gene_variant MODIFIER c.*3382C>T| S180
5 BAA05g29370 A05 32875772 G A downstream_gene_variant MODIFIER c.*2121C>T| S6
6 BAA05g29370 A05 32876173 G A downstream_gene_variant MODIFIER c.*1720C>T| S305
7 BAA05g29370 A05 32877336 C T downstream_gene_variant MODIFIER c.*557G>A| S183
S198
8 BAA05g29370 A05 32878692 C T splice_acceptor_variant&intron_variant HIGH c.3225-1G>A| S108
9 BAA05g29370 A05 32878893 C T missense_variant MODERATE c.3139G>A|p.Gly1047Ser S2
10 BAA05g29370 A05 32880863 C T missense_variant MODERATE c.1936G>A|p.Gly646Arg S289
11 BAA05g29370 A05 32881278 C T stop_gained HIGH c.1521G>A|p.Trp507* S206
S239
S26
12 BAA05g29370 A05 32881306 G A missense_variant MODERATE c.1493C>T|p.Ala498Val S156
13 BAA05g29370 A05 32881795 G A missense_variant MODERATE c.1252C>T|p.His418Tyr S104
S52
14 BAA05g29370 A05 32881838 G A synonymous_variant LOW c.1209C>T|p.Ala403Ala S262
15 BAA05g29370 A05 32882678 G A synonymous_variant LOW c.585C>T|p.Leu195Leu S77
S82
16 BAA05g29370 A05 32884081 G A upstream_gene_variant MODIFIER c.-545C>T| S144
17 BAA05g29370 A05 32886556 C T upstream_gene_variant MODIFIER c.-3020G>A| S259
18 BAA05g29370 A05 32886813 G A upstream_gene_variant MODIFIER c.-3277C>T| S37