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 BAA01g39990 A01 26559272 C T downstream_gene_variant MODIFIER c.*2087G>A| S205
2 BAA01g39990 A01 26559744 G A downstream_gene_variant MODIFIER c.*1615C>T| S105
S106
3 BAA01g39990 A01 26560743 G A downstream_gene_variant MODIFIER c.*616C>T| S163
4 BAA01g39990 A01 26561975 G A intron_variant MODIFIER c.1643-32C>T| S8
5 BAA01g39990 A01 26562530 G A intron_variant MODIFIER c.1377-143C>T| S195
6 BAA01g39990 A01 26563167 C T synonymous_variant LOW c.1026G>A|p.Lys342Lys S230
7 BAA01g39990 A01 26563945 G T intron_variant MODIFIER c.651-10C>A| S149
8 BAA01g39990 A01 26563946 A T intron_variant MODIFIER c.651-11T>A| S149
9 BAA01g39990 A01 26564536 C T missense_variant&splice_region_variant MODERATE c.448G>A|p.Glu150Lys S198
10 BAA01g39990 A01 26564759 C T intron_variant MODIFIER c.322-97G>A| S203
11 BAA01g39990 A01 26564888 C T intron_variant MODIFIER c.321+218G>A| S139
12 BAA01g39990 A01 26564958 C T intron_variant MODIFIER c.321+148G>A| S159
S243
13 BAA01g39990 A01 26565274 C T synonymous_variant LOW c.153G>A|p.Lys51Lys S39
14 BAA01g39990 A01 26565371 G A missense_variant MODERATE c.56C>T|p.Ala19Val S245
15 BAA01g39990 A01 26568966 C T upstream_gene_variant MODIFIER c.-3540G>A| S148
S30
S31
16 BAA01g39990 A01 26569060 C T upstream_gene_variant MODIFIER c.-3634G>A| S264
17 BAA01g39990 A01 26570027 C T upstream_gene_variant MODIFIER c.-4601G>A| S206
S26