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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g15100 A02 7220332 C T upstream_gene_variant MODIFIER c.-4502C>T| S1
S90
2 BAA02g15100 A02 7220515 C T upstream_gene_variant MODIFIER c.-4319C>T| S47
3 BAA02g15100 A02 7220994 G A upstream_gene_variant MODIFIER c.-3840G>A| S2
4 BAA02g15100 A02 7221197 C T upstream_gene_variant MODIFIER c.-3637C>T| S179
5 BAA02g15100 A02 7221363 G A upstream_gene_variant MODIFIER c.-3471G>A| S67
6 BAA02g15100 A02 7222084 C T upstream_gene_variant MODIFIER c.-2750C>T| S199
7 BAA02g15100 A02 7223108 G A upstream_gene_variant MODIFIER c.-1726G>A| S169
8 BAA02g15100 A02 7223967 G A upstream_gene_variant MODIFIER c.-867G>A| S272
9 BAA02g15100 A02 7223996 C T upstream_gene_variant MODIFIER c.-838C>T| S276
10 BAA02g15100 A02 7224341 G A upstream_gene_variant MODIFIER c.-493G>A| S38
11 BAA02g15100 A02 7224687 C T upstream_gene_variant MODIFIER c.-147C>T| S183
S198
12 BAA02g15100 A02 7224711 G A upstream_gene_variant MODIFIER c.-123G>A| S4
13 BAA02g15100 A02 7225318 G A missense_variant MODERATE c.485G>A|p.Gly162Glu S155
S211
14 BAA02g15100 A02 7225712 G A intron_variant MODIFIER c.606+273G>A| S204
15 BAA02g15100 A02 7226435 C A synonymous_variant LOW c.792C>A|p.Leu264Leu S49
16 BAA02g15100 A02 7228053 G A stop_gained HIGH c.1380G>A|p.Trp460* S261