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 BAA09g26480 A09 17201472 G A upstream_gene_variant MODIFIER c.-4471G>A| S216
2 BAA09g26480 A09 17201491 G A upstream_gene_variant MODIFIER c.-4452G>A| S298
3 BAA09g26480 A09 17201626 T C upstream_gene_variant MODIFIER c.-4317T>C| S111
4 BAA09g26480 A09 17201748 G A upstream_gene_variant MODIFIER c.-4195G>A| S111
5 BAA09g26480 A09 17202260 G A upstream_gene_variant MODIFIER c.-3683G>A| S213
6 BAA09g26480 A09 17203141 C T upstream_gene_variant MODIFIER c.-2802C>T| S186
7 BAA09g26480 A09 17203473 C T upstream_gene_variant MODIFIER c.-2470C>T| S260
8 BAA09g26480 A09 17204019 C T upstream_gene_variant MODIFIER c.-1924C>T| S231
9 BAA09g26480 A09 17204440 C T upstream_gene_variant MODIFIER c.-1503C>T| S206
S26
10 BAA09g26480 A09 17204470 C T upstream_gene_variant MODIFIER c.-1473C>T| S103
11 BAA09g26480 A09 17206346 C T missense_variant MODERATE c.404C>T|p.Thr135Ile S173
12 BAA09g26480 A09 17206489 C T missense_variant MODERATE c.547C>T|p.Pro183Ser S242
13 BAA09g26480 A09 17206706 G A missense_variant MODERATE c.764G>A|p.Gly255Glu S41
14 BAA09g26480 A09 17206902 G A synonymous_variant LOW c.960G>A|p.Gln320Gln S288
S97