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 BAA05g11120 A05 5636403 G A synonymous_variant LOW c.3747C>T|p.Phe1249Phe S192
2 BAA05g11120 A05 5636727 G A synonymous_variant LOW c.3423C>T|p.Ala1141Ala S180
3 BAA05g11120 A05 5637240 G A missense_variant MODERATE c.3073C>T|p.His1025Tyr S32
4 BAA05g11120 A05 5639314 G A missense_variant MODERATE c.2072C>T|p.Thr691Met S179
5 BAA05g11120 A05 5639860 C T missense_variant MODERATE c.1681G>A|p.Ala561Thr S117
6 BAA05g11120 A05 5641112 G A splice_region_variant&intron_variant LOW c.1018+6C>T| S292
7 BAA05g11120 A05 5641221 C T missense_variant MODERATE c.915G>A|p.Met305Ile S99
8 BAA05g11120 A05 5641249 G A missense_variant MODERATE c.887C>T|p.Ser296Leu S180
9 BAA05g11120 A05 5641792 C T missense_variant MODERATE c.344G>A|p.Gly115Asp S28
10 BAA05g11120 A05 5642210 G A upstream_gene_variant MODIFIER c.-75C>T| S298
11 BAA05g11120 A05 5642726 C T upstream_gene_variant MODIFIER c.-591G>A| S87
12 BAA05g11120 A05 5642761 G A upstream_gene_variant MODIFIER c.-626C>T| S66
13 BAA05g11120 A05 5646904 C T upstream_gene_variant MODIFIER c.-4769G>A| S30
S31