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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g44890 A02 36844883 C T downstream_gene_variant MODIFIER c.*1805G>A| S19
2 BAA02g44890 A02 36846760 G A synonymous_variant LOW c.720C>T|p.Val240Val S136
3 BAA02g44890 A02 36847360 G A missense_variant MODERATE c.379C>T|p.Leu127Phe S60
4 BAA02g44890 A02 36847544 G A synonymous_variant LOW c.195C>T|p.Leu65Leu S36
5 BAA02g44890 A02 36849345 C T upstream_gene_variant MODIFIER c.-1607G>A| S202
6 BAA02g44890 A02 36849582 G A upstream_gene_variant MODIFIER c.-1844C>T| S268
7 BAA02g44890 A02 36850090 A G upstream_gene_variant MODIFIER c.-2352T>C| S244
8 BAA02g44890 A02 36850727 G A upstream_gene_variant MODIFIER c.-2989C>T| S293
9 BAA02g44890 A02 36850815 G A upstream_gene_variant MODIFIER c.-3077C>T| S66
10 BAA02g44890 A02 36850966 G A upstream_gene_variant MODIFIER c.-3228C>T| S155
S211
11 BAA02g44890 A02 36851113 C T upstream_gene_variant MODIFIER c.-3375G>A| S34
12 BAA02g44890 A02 36851273 C T upstream_gene_variant MODIFIER c.-3535G>A| S252
13 BAA02g44890 A02 36851396 C T upstream_gene_variant MODIFIER c.-3658G>A| S299
14 BAA02g44890 A02 36851504 C T upstream_gene_variant MODIFIER c.-3766G>A| S32
15 BAA02g44890 A02 36851861 C T upstream_gene_variant MODIFIER c.-4123G>A| S6
16 BAA02g44890 A02 36851880 C T upstream_gene_variant MODIFIER c.-4142G>A| S67
17 BAA02g44890 A02 36852043 C T upstream_gene_variant MODIFIER c.-4305G>A| S173