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


Gene ID

Results: 1 - 38 of 38 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g06500 A07 15893103 G A downstream_gene_variant MODIFIER c.*4894C>T| S71
2 BAA07g06500 A07 15893788 C T downstream_gene_variant MODIFIER c.*4209G>A| S165
3 BAA07g06500 A07 15893792 G A downstream_gene_variant MODIFIER c.*4205C>T| S237
4 BAA07g06500 A07 15894111 C T downstream_gene_variant MODIFIER c.*3886G>A| S187
5 BAA07g06500 A07 15894857 C T downstream_gene_variant MODIFIER c.*3140G>A| S132
S288
6 BAA07g06500 A07 15895043 C T downstream_gene_variant MODIFIER c.*2954G>A| S35
7 BAA07g06500 A07 15896474 G A downstream_gene_variant MODIFIER c.*1523C>T| S25
8 BAA07g06500 A07 15896788 G A downstream_gene_variant MODIFIER c.*1209C>T| S142
9 BAA07g06500 A07 15896872 C T downstream_gene_variant MODIFIER c.*1125G>A| S136
S186
S275
10 BAA07g06500 A07 15897249 G A downstream_gene_variant MODIFIER c.*748C>T| S283
11 BAA07g06500 A07 15897631 G A downstream_gene_variant MODIFIER c.*366C>T| S182
12 BAA07g06500 A07 15897738 C T downstream_gene_variant MODIFIER c.*259G>A| S70
13 BAA07g06500 A07 15897765 C T downstream_gene_variant MODIFIER c.*232G>A| S162
14 BAA07g06500 A07 15899066 G A missense_variant MODERATE c.983C>T|p.Ala328Val S50
15 BAA07g06500 A07 15899231 G A missense_variant MODERATE c.818C>T|p.Pro273Leu S117
16 BAA07g06500 A07 15899718 G A missense_variant MODERATE c.331C>T|p.Leu111Phe S161
17 BAA07g06500 A07 15900208 C T upstream_gene_variant MODIFIER c.-160G>A| S187
S188
S298
18 BAA07g06500 A07 15900269 C T upstream_gene_variant MODIFIER c.-221G>A| S263
19 BAA07g06500 A07 15900306 G A upstream_gene_variant MODIFIER c.-258C>T| S19
S71
20 BAA07g06500 A07 15900536 C T upstream_gene_variant MODIFIER c.-488G>A| S298
21 BAA07g06500 A07 15900729 G A upstream_gene_variant MODIFIER c.-681C>T| S62
22 BAA07g06500 A07 15900754 C T upstream_gene_variant MODIFIER c.-706G>A| S126
23 BAA07g06500 A07 15900761 C T upstream_gene_variant MODIFIER c.-713G>A| S1
S90
24 BAA07g06500 A07 15901795 C T upstream_gene_variant MODIFIER c.-1747G>A| S42
25 BAA07g06500 A07 15902194 C T upstream_gene_variant MODIFIER c.-2146G>A| S155
S211