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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g10960 A10 12712066 G A downstream_gene_variant MODIFIER c.*4643C>T| S257
2 BAA10g10960 A10 12712291 T G downstream_gene_variant MODIFIER c.*4418A>C| S257
3 BAA10g10960 A10 12712329 G A downstream_gene_variant MODIFIER c.*4380C>T| S57
4 BAA10g10960 A10 12713736 G A downstream_gene_variant MODIFIER c.*2973C>T| S150
5 BAA10g10960 A10 12714384 C T downstream_gene_variant MODIFIER c.*2325G>A| S70
6 BAA10g10960 A10 12714423 C T downstream_gene_variant MODIFIER c.*2286G>A| S259
7 BAA10g10960 A10 12714610 G A downstream_gene_variant MODIFIER c.*2099C>T| S45
8 BAA10g10960 A10 12714989 C T downstream_gene_variant MODIFIER c.*1720G>A| S180
9 BAA10g10960 A10 12715317 C T downstream_gene_variant MODIFIER c.*1392G>A| S185
10 BAA10g10960 A10 12715823 C T downstream_gene_variant MODIFIER c.*886G>A| S165
S211
S227
11 BAA10g10960 A10 12716565 C T downstream_gene_variant MODIFIER c.*144G>A| S84
S93
12 BAA10g10960 A10 12716589 C T downstream_gene_variant MODIFIER c.*120G>A| S255
13 BAA10g10960 A10 12716746 C T missense_variant MODERATE c.1418G>A|p.Gly473Glu S19
14 BAA10g10960 A10 12716844 C T synonymous_variant LOW c.1320G>A|p.Lys440Lys S87
15 BAA10g10960 A10 12716951 C T missense_variant MODERATE c.1213G>A|p.Val405Ile S161
S289
16 BAA10g10960 A10 12717656 C T missense_variant MODERATE c.598G>A|p.Glu200Lys S135
17 BAA10g10960 A10 12717707 C T missense_variant MODERATE c.547G>A|p.Glu183Lys S37
18 BAA10g10960 A10 12718140 C T synonymous_variant LOW c.216G>A|p.Leu72Leu S95
19 BAA10g10960 A10 12719655 G A upstream_gene_variant MODIFIER c.-1300C>T| S79
S84
20 BAA10g10960 A10 12720421 G A upstream_gene_variant MODIFIER c.-2066C>T| S286
21 BAA10g10960 A10 12723274 C T upstream_gene_variant MODIFIER c.-4919G>A| S80
22 BAA10g10960 A10 12723313 G A upstream_gene_variant MODIFIER c.-4958C>T| S290
23 BAA10g10960 A10 12723334 G A upstream_gene_variant MODIFIER c.-4979C>T| S148
S30
S31