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 BAA02g22690 A02 12300271 C T downstream_gene_variant MODIFIER c.*4371G>A| S299
2 BAA02g22690 A02 12300544 C T downstream_gene_variant MODIFIER c.*4098G>A| S33
3 BAA02g22690 A02 12300793 C T downstream_gene_variant MODIFIER c.*3849G>A| S64
4 BAA02g22690 A02 12300848 C T downstream_gene_variant MODIFIER c.*3794G>A| S301
S304
5 BAA02g22690 A02 12301253 C T downstream_gene_variant MODIFIER c.*3389G>A| S267
6 BAA02g22690 A02 12301645 G A downstream_gene_variant MODIFIER c.*2997C>T| S4
7 BAA02g22690 A02 12301751 C T downstream_gene_variant MODIFIER c.*2891G>A| S242
8 BAA02g22690 A02 12304748 C T missense_variant MODERATE c.542G>A|p.Arg181His S209
9 BAA02g22690 A02 12304754 C T missense_variant MODERATE c.536G>A|p.Ser179Asn S53
10 BAA02g22690 A02 12304763 G A missense_variant MODERATE c.527C>T|p.Ala176Val S81
S85
11 BAA02g22690 A02 12305142 C T synonymous_variant LOW c.327G>A|p.Thr109Thr S15
S156
S3
S34
12 BAA02g22690 A02 12305402 C T stop_gained HIGH c.147G>A|p.Trp49* S33
13 BAA02g22690 A02 12305808 C T upstream_gene_variant MODIFIER c.-260G>A| S32
14 BAA02g22690 A02 12306065 C T upstream_gene_variant MODIFIER c.-517G>A| S219
S72
15 BAA02g22690 A02 12306078 G A upstream_gene_variant MODIFIER c.-530C>T| S155
S211
16 BAA02g22690 A02 12306153 C T upstream_gene_variant MODIFIER c.-605G>A| S32
17 BAA02g22690 A02 12307665 C T upstream_gene_variant MODIFIER c.-2117G>A| S118
18 BAA02g22690 A02 12308041 C T upstream_gene_variant MODIFIER c.-2493G>A| S202
19 BAA02g22690 A02 12308623 C T upstream_gene_variant MODIFIER c.-3075G>A| S171
20 BAA02g22690 A02 12308908 C T upstream_gene_variant MODIFIER c.-3360G>A| S186
21 BAA02g22690 A02 12309401 T G upstream_gene_variant MODIFIER c.-3853A>C| S126
S221
S244
S246
S84
22 BAA02g22690 A02 12309408 G A upstream_gene_variant MODIFIER c.-3860C>T| S298
23 BAA02g22690 A02 12310236 C T upstream_gene_variant MODIFIER c.-4688G>A| S277