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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g03610 A02 1591988 C T upstream_gene_variant MODIFIER c.-4994C>T| S153
S213
2 BAA02g03610 A02 1592182 C T upstream_gene_variant MODIFIER c.-4800C>T| S60
3 BAA02g03610 A02 1592534 G A upstream_gene_variant MODIFIER c.-4448G>A| S47
4 BAA02g03610 A02 1592602 C T upstream_gene_variant MODIFIER c.-4380C>T| S298
5 BAA02g03610 A02 1592843 G A upstream_gene_variant MODIFIER c.-4139G>A| S183
S198
6 BAA02g03610 A02 1592849 G A upstream_gene_variant MODIFIER c.-4133G>A| S35
7 BAA02g03610 A02 1592870 G A upstream_gene_variant MODIFIER c.-4112G>A| S143
8 BAA02g03610 A02 1593435 C T upstream_gene_variant MODIFIER c.-3547C>T| S249
9 BAA02g03610 A02 1593661 G A upstream_gene_variant MODIFIER c.-3321G>A| S68
10 BAA02g03610 A02 1593670 C T upstream_gene_variant MODIFIER c.-3312C>T| S171
11 BAA02g03610 A02 1593915 C T upstream_gene_variant MODIFIER c.-3067C>T| S209
12 BAA02g03610 A02 1594053 C T upstream_gene_variant MODIFIER c.-2929C>T| S274
13 BAA02g03610 A02 1594368 G A upstream_gene_variant MODIFIER c.-2614G>A| S136
14 BAA02g03610 A02 1594547 C T upstream_gene_variant MODIFIER c.-2435C>T| S223
15 BAA02g03610 A02 1594746 C T upstream_gene_variant MODIFIER c.-2236C>T| S5
16 BAA02g03610 A02 1595026 G A upstream_gene_variant MODIFIER c.-1956G>A| S263
17 BAA02g03610 A02 1596507 C G upstream_gene_variant MODIFIER c.-475C>G| S182
18 BAA02g03610 A02 1596551 C T upstream_gene_variant MODIFIER c.-431C>T| S75
19 BAA02g03610 A02 1597006 G A missense_variant MODERATE c.25G>A|p.Val9Ile S209
20 BAA02g03610 A02 1597188 C T synonymous_variant LOW c.207C>T|p.Asn69Asn S183
S198
21 BAA02g03610 A02 1597190 G A missense_variant MODERATE c.209G>A|p.Arg70His S45
22 BAA02g03610 A02 1597841 C T missense_variant MODERATE c.449C>T|p.Ala150Val S124
23 BAA02g03610 A02 1598058 C T synonymous_variant LOW c.666C>T|p.Ile222Ile S104
24 BAA02g03610 A02 1598919 C T missense_variant MODERATE c.1190C>T|p.Ser397Leu S61
25 BAA02g03610 A02 1599935 G A downstream_gene_variant MODIFIER c.*721G>A| S26