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 BAA05g29990 A05 33248288 C T synonymous_variant LOW c.126C>T|p.Ser42Ser S89
2 BAA05g29990 A05 33248403 G A missense_variant MODERATE c.241G>A|p.Ala81Thr S262
3 BAA05g29990 A05 33248527 C T missense_variant MODERATE c.365C>T|p.Pro122Leu S264
4 BAA05g29990 A05 33248992 G A missense_variant MODERATE c.754G>A|p.Glu252Lys S76
5 BAA05g29990 A05 33249360 C T synonymous_variant LOW c.1122C>T|p.Phe374Phe S74
6 BAA05g29990 A05 33249944 G A missense_variant MODERATE c.1540G>A|p.Val514Ile S266
7 BAA05g29990 A05 33250230 C T missense_variant&splice_region_variant MODERATE c.1826C>T|p.Ser609Phe S148
S210
S30
S31
8 BAA05g29990 A05 33251988 C T splice_region_variant&intron_variant LOW c.2828-3C>T| S302
9 BAA05g29990 A05 33255175 G A downstream_gene_variant MODIFIER c.*2394G>A| S173
10 BAA05g29990 A05 33256169 C T downstream_gene_variant MODIFIER c.*3388C>T| S177
S249
11 BAA05g29990 A05 33256711 G A downstream_gene_variant MODIFIER c.*3930G>A| S194
12 BAA05g29990 A05 33256891 G A downstream_gene_variant MODIFIER c.*4110G>A| S50
13 BAA05g29990 A05 33257633 C T downstream_gene_variant MODIFIER c.*4852C>T| S207