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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g30230 A02 17571795 G A upstream_gene_variant MODIFIER c.-4977G>A| S34
2 BAA02g30230 A02 17572089 C T upstream_gene_variant MODIFIER c.-4683C>T| S262
3 BAA02g30230 A02 17572261 G A upstream_gene_variant MODIFIER c.-4511G>A| S155
S211
4 BAA02g30230 A02 17573215 C T upstream_gene_variant MODIFIER c.-3557C>T| S201
5 BAA02g30230 A02 17574760 G A upstream_gene_variant MODIFIER c.-2012G>A| S5
6 BAA02g30230 A02 17576329 G A upstream_gene_variant MODIFIER c.-443G>A| S228
7 BAA02g30230 A02 17576449 C T upstream_gene_variant MODIFIER c.-323C>T| S270
8 BAA02g30230 A02 17576675 C T upstream_gene_variant MODIFIER c.-97C>T| S301
S304
9 BAA02g30230 A02 17576750 C T upstream_gene_variant MODIFIER c.-22C>T| S15
S3
10 BAA02g30230 A02 17576815 C T missense_variant MODERATE c.44C>T|p.Ser15Phe S160
11 BAA02g30230 A02 17577403 G A missense_variant MODERATE c.632G>A|p.Arg211Lys S155
S211
12 BAA02g30230 A02 17577513 G A missense_variant MODERATE c.742G>A|p.Glu248Lys S251
13 BAA02g30230 A02 17577876 C T splice_region_variant&intron_variant LOW c.808-3C>T| S275
14 BAA02g30230 A02 17578337 G A splice_region_variant&intron_variant LOW c.1182+5G>A| S79
S91