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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g38160 A09 46155267 A C intron_variant MODIFIER c.1179+37T>G|
2 BAA09g38160 A09 46155268 C T intron_variant MODIFIER c.1179+36G>A| S228
3 BAA09g38160 A09 46156787 G A missense_variant MODERATE c.241C>T|p.Pro81Ser S266
4 BAA09g38160 A09 46156919 C T intron_variant MODIFIER c.211-102G>A| S19
5 BAA09g38160 A09 46157750 G A upstream_gene_variant MODIFIER c.-102C>T| S70
6 BAA09g38160 A09 46158142 G A upstream_gene_variant MODIFIER c.-494C>T| S197
7 BAA09g38160 A09 46159329 A T upstream_gene_variant MODIFIER c.-1681T>A| S262
8 BAA09g38160 A09 46159610 G A upstream_gene_variant MODIFIER c.-1962C>T| S107
9 BAA09g38160 A09 46159765 G A upstream_gene_variant MODIFIER c.-2117C>T| S59
10 BAA09g38160 A09 46160797 C T upstream_gene_variant MODIFIER c.-3149G>A| S247
11 BAA09g38160 A09 46160831 G A upstream_gene_variant MODIFIER c.-3183C>T| S291
12 BAA09g38160 A09 46161923 C T upstream_gene_variant MODIFIER c.-4275G>A| S240
13 BAA09g38160 A09 46162297 C T upstream_gene_variant MODIFIER c.-4649G>A| S179
14 BAA09g38160 A09 46162426 C T upstream_gene_variant MODIFIER c.-4778G>A| S104
S52