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 BAA04g02680 A04 1595547 G A upstream_gene_variant MODIFIER c.-3919G>A| S25
2 BAA04g02680 A04 1596105 C T upstream_gene_variant MODIFIER c.-3361C>T| S246
3 BAA04g02680 A04 1596980 C T upstream_gene_variant MODIFIER c.-2486C>T| S171
4 BAA04g02680 A04 1597491 G A upstream_gene_variant MODIFIER c.-1975G>A| S208
5 BAA04g02680 A04 1597949 C T upstream_gene_variant MODIFIER c.-1517C>T| S129
6 BAA04g02680 A04 1598044 C T upstream_gene_variant MODIFIER c.-1422C>T| S226
7 BAA04g02680 A04 1598089 C T upstream_gene_variant MODIFIER c.-1377C>T| S82
S92
8 BAA04g02680 A04 1598362 G A upstream_gene_variant MODIFIER c.-1104G>A| S79
S91
9 BAA04g02680 A04 1598751 C T upstream_gene_variant MODIFIER c.-715C>T| S35
10 BAA04g02680 A04 1599357 C T upstream_gene_variant MODIFIER c.-109C>T| S73
11 BAA04g02680 A04 1600321 C T intron_variant MODIFIER c.138+718C>T| S159
S299
12 BAA04g02680 A04 1600400 C T intron_variant MODIFIER c.138+797C>T| S39
13 BAA04g02680 A04 1605096 C T missense_variant MODERATE c.1151C>T|p.Thr384Ile S156
S2
S4
14 BAA04g02680 A04 1605136 C T synonymous_variant LOW c.1191C>T|p.Asp397Asp S283