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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g16510 A06 8215501 G A upstream_gene_variant MODIFIER c.-3096G>A| S209
2 BAA06g16510 A06 8216140 A T upstream_gene_variant MODIFIER c.-2457A>T| S87
3 BAA06g16510 A06 8216343 G A upstream_gene_variant MODIFIER c.-2254G>A| S133
4 BAA06g16510 A06 8216894 C T upstream_gene_variant MODIFIER c.-1703C>T| S14
5 BAA06g16510 A06 8217060 C T upstream_gene_variant MODIFIER c.-1537C>T| S115
6 BAA06g16510 A06 8217074 C T upstream_gene_variant MODIFIER c.-1523C>T| S294
7 BAA06g16510 A06 8217402 C T upstream_gene_variant MODIFIER c.-1195C>T| S303
8 BAA06g16510 A06 8217440 G A upstream_gene_variant MODIFIER c.-1157G>A| S209
9 BAA06g16510 A06 8217514 G A upstream_gene_variant MODIFIER c.-1083G>A| S149
10 BAA06g16510 A06 8217623 G A upstream_gene_variant MODIFIER c.-974G>A| S274
11 BAA06g16510 A06 8218088 G A upstream_gene_variant MODIFIER c.-509G>A| S81
12 BAA06g16510 A06 8218772 G A missense_variant MODERATE c.176G>A|p.Gly59Glu S177
13 BAA06g16510 A06 8219077 C T intron_variant MODIFIER c.186+295C>T| S212
14 BAA06g16510 A06 8219089 C T intron_variant MODIFIER c.187-285C>T| S12
15 BAA06g16510 A06 8219364 C T intron_variant MODIFIER c.187-10C>T| S135
16 BAA06g16510 A06 8219380 G A missense_variant MODERATE c.193G>A|p.Gly65Ser S81
S85
17 BAA06g16510 A06 8219776 C T intron_variant MODIFIER c.235-165C>T| S159
S243
S299
18 BAA06g16510 A06 8219806 G A intron_variant MODIFIER c.235-135G>A| S173
19 BAA06g16510 A06 8220105 C T intron_variant MODIFIER c.289-104C>T| S96
20 BAA06g16510 A06 8221173 G A downstream_gene_variant MODIFIER c.*269G>A| S179
21 BAA06g16510 A06 8221495 G A downstream_gene_variant MODIFIER c.*591G>A| S173
22 BAA06g16510 A06 8222272 G A downstream_gene_variant MODIFIER c.*1368G>A| S88
23 BAA06g16510 A06 8224805 C T downstream_gene_variant MODIFIER c.*3901C>T| S237
24 BAA06g16510 A06 8225817 C T downstream_gene_variant MODIFIER c.*4913C>T| S298
25 BAA06g16510 A06 8225831 G A downstream_gene_variant MODIFIER c.*4927G>A| S9