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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g41010 A09 47889782 C T upstream_gene_variant MODIFIER c.-4953C>T| S28
2 BAA09g41010 A09 47889861 C T upstream_gene_variant MODIFIER c.-4874C>T| S81
S85
3 BAA09g41010 A09 47890102 G A upstream_gene_variant MODIFIER c.-4633G>A| S10
4 BAA09g41010 A09 47890252 C T upstream_gene_variant MODIFIER c.-4483C>T| S208
S219
5 BAA09g41010 A09 47891194 C T upstream_gene_variant MODIFIER c.-3541C>T| S228
6 BAA09g41010 A09 47891227 G A upstream_gene_variant MODIFIER c.-3508G>A| S178
7 BAA09g41010 A09 47895543 C T missense_variant MODERATE c.809C>T|p.Pro270Leu S211
S227
8 BAA09g41010 A09 47895816 C T synonymous_variant LOW c.867C>T|p.Tyr289Tyr S7
9 BAA09g41010 A09 47896336 C T splice_region_variant&intron_variant LOW c.1307-8C>T| S80
10 BAA09g41010 A09 47896960 C T missense_variant MODERATE c.1634C>T|p.Ser545Phe S191
11 BAA09g41010 A09 47897144 C T splice_region_variant&intron_variant LOW c.1735-5C>T| S109
12 BAA09g41010 A09 47897168 G A missense_variant MODERATE c.1754G>A|p.Arg585Lys S255
13 BAA09g41010 A09 47897271 C T synonymous_variant LOW c.1857C>T|p.Cys619Cys S297
14 BAA09g41010 A09 47897455 G A missense_variant MODERATE c.1940G>A|p.Ser647Asn S175
S177
15 BAA09g41010 A09 47898005 G A downstream_gene_variant MODIFIER c.*348G>A| S185