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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g39230 A09 46868605 C T intron_variant MODIFIER c.1986+72G>A| S232
2 BAA09g39230 A09 46869263 G A missense_variant MODERATE c.1765C>T|p.Pro589Ser S42
3 BAA09g39230 A09 46869989 C T missense_variant MODERATE c.1387G>A|p.Gly463Ser S32
4 BAA09g39230 A09 46870201 G A missense_variant MODERATE c.1175C>T|p.Ser392Phe S132
S215
5 BAA09g39230 A09 46870211 C T missense_variant MODERATE c.1165G>A|p.Ala389Thr S144
6 BAA09g39230 A09 46870700 C T intron_variant MODIFIER c.888+32G>A| S192
7 BAA09g39230 A09 46870830 C T intron_variant MODIFIER c.821-31G>A| S205
8 BAA09g39230 A09 46871940 C T missense_variant MODERATE c.188G>A|p.Gly63Asp S256
9 BAA09g39230 A09 46872612 G A intron_variant MODIFIER c.104+183C>T| S38
10 BAA09g39230 A09 46872624 G A intron_variant MODIFIER c.104+171C>T| S180
11 BAA09g39230 A09 46873622 G A upstream_gene_variant MODIFIER c.-724C>T| S162
12 BAA09g39230 A09 46876049 G A upstream_gene_variant MODIFIER c.-3151C>T| S308
13 BAA09g39230 A09 46876501 C T upstream_gene_variant MODIFIER c.-3603G>A| S236
14 BAA09g39230 A09 46876713 C T upstream_gene_variant MODIFIER c.-3815G>A| S247
15 BAA09g39230 A09 46876729 C T upstream_gene_variant MODIFIER c.-3831G>A| S205
16 BAA09g39230 A09 46876957 C T upstream_gene_variant MODIFIER c.-4059G>A| S138
17 BAA09g39230 A09 46877633 G A upstream_gene_variant MODIFIER c.-4735C>T| S127
18 BAA09g39230 A09 46877646 G A upstream_gene_variant MODIFIER c.-4748C>T| S124
19 BAA09g39230 A09 46877755 C T upstream_gene_variant MODIFIER c.-4857G>A| S36