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 BAA10g05060 A10 2602307 G A upstream_gene_variant MODIFIER c.-4364G>A| S161
2 BAA10g05060 A10 2603948 C T upstream_gene_variant MODIFIER c.-2723C>T| S204
3 BAA10g05060 A10 2604821 G A upstream_gene_variant MODIFIER c.-1850G>A| S148
S210
S30
S31
4 BAA10g05060 A10 2604933 G A upstream_gene_variant MODIFIER c.-1738G>A| S237
5 BAA10g05060 A10 2605288 G A upstream_gene_variant MODIFIER c.-1383G>A| S292
6 BAA10g05060 A10 2605398 C T upstream_gene_variant MODIFIER c.-1273C>T| S142
S170
7 BAA10g05060 A10 2605527 G A upstream_gene_variant MODIFIER c.-1144G>A| S292
8 BAA10g05060 A10 2605613 G A upstream_gene_variant MODIFIER c.-1058G>A| S128
9 BAA10g05060 A10 2605862 G A upstream_gene_variant MODIFIER c.-809G>A| S57
10 BAA10g05060 A10 2606531 G A upstream_gene_variant MODIFIER c.-140G>A| S17
11 BAA10g05060 A10 2606762 C T missense_variant MODERATE c.92C>T|p.Pro31Leu S171
12 BAA10g05060 A10 2607616 A C synonymous_variant LOW c.946A>C|p.Arg316Arg S302
13 BAA10g05060 A10 2607809 G A missense_variant MODERATE c.1139G>A|p.Gly380Glu S130
14 BAA10g05060 A10 2607982 G A missense_variant MODERATE c.1312G>A|p.Gly438Arg S45
15 BAA10g05060 A10 2608979 G A missense_variant MODERATE c.2122G>A|p.Glu708Lys S211
S227