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 BAA09g17360 A09 10346032 C T upstream_gene_variant MODIFIER c.-2898C>T| S48
2 BAA09g17360 A09 10346321 C T upstream_gene_variant MODIFIER c.-2609C>T| S242
3 BAA09g17360 A09 10346707 C T upstream_gene_variant MODIFIER c.-2223C>T| S116
4 BAA09g17360 A09 10347633 G A upstream_gene_variant MODIFIER c.-1297G>A| S182
5 BAA09g17360 A09 10348292 G A upstream_gene_variant MODIFIER c.-638G>A| S210
6 BAA09g17360 A09 10348515 C T upstream_gene_variant MODIFIER c.-415C>T| S281
7 BAA09g17360 A09 10349056 C T missense_variant MODERATE c.127C>T|p.Pro43Ser S208
S93
8 BAA09g17360 A09 10349075 G A missense_variant MODERATE c.146G>A|p.Arg49Lys S95
9 BAA09g17360 A09 10351277 G A missense_variant MODERATE c.1274G>A|p.Arg425Lys S273
10 BAA09g17360 A09 10352141 C T intron_variant MODIFIER c.1525+43C>T| S13
S278
S279
11 BAA09g17360 A09 10352435 G A intron_variant MODIFIER c.1525+337G>A| S130
12 BAA09g17360 A09 10352760 G A intron_variant MODIFIER c.1525+662G>A| S210
13 BAA09g17360 A09 10352983 G A intron_variant MODIFIER c.1525+885G>A| S194
14 BAA09g17360 A09 10355724 C T missense_variant MODERATE c.1661C>T|p.Thr554Ile S232