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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g37190 A02 31890159 C T downstream_gene_variant MODIFIER c.*4872G>A| S123
2 BAA02g37190 A02 31890849 G A downstream_gene_variant MODIFIER c.*4182C>T| S113
3 BAA02g37190 A02 31891345 G A downstream_gene_variant MODIFIER c.*3686C>T| S125
4 BAA02g37190 A02 31892071 G A downstream_gene_variant MODIFIER c.*2960C>T| S281
5 BAA02g37190 A02 31892326 A T downstream_gene_variant MODIFIER c.*2705T>A| S230
6 BAA02g37190 A02 31893380 C T downstream_gene_variant MODIFIER c.*1651G>A| S205
7 BAA02g37190 A02 31894233 G A downstream_gene_variant MODIFIER c.*798C>T| S48
8 BAA02g37190 A02 31894260 G A downstream_gene_variant MODIFIER c.*771C>T| S114
9 BAA02g37190 A02 31894559 G A downstream_gene_variant MODIFIER c.*472C>T| S224
10 BAA02g37190 A02 31895231 G A synonymous_variant LOW c.1336C>T|p.Leu446Leu S72
S78
11 BAA02g37190 A02 31895511 G A synonymous_variant LOW c.1056C>T|p.Phe352Phe S278
12 BAA02g37190 A02 31896236 G A intron_variant MODIFIER c.642-311C>T| S36
13 BAA02g37190 A02 31896346 C T intron_variant MODIFIER c.642-421G>A| S201
14 BAA02g37190 A02 31896545 C T intron_variant MODIFIER c.641+375G>A| S203
15 BAA02g37190 A02 31897066 C T synonymous_variant LOW c.495G>A|p.Lys165Lys S124
16 BAA02g37190 A02 31897305 C T missense_variant MODERATE c.256G>A|p.Glu86Lys S189
17 BAA02g37190 A02 31897773 G A missense_variant MODERATE c.44C>T|p.Ser15Phe S82
S92
18 BAA02g37190 A02 31898231 G A upstream_gene_variant MODIFIER c.-415C>T| S35
19 BAA02g37190 A02 31898309 C T upstream_gene_variant MODIFIER c.-493G>A| S162
20 BAA02g37190 A02 31899042 G A upstream_gene_variant MODIFIER c.-1226C>T| S99