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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g57440 A09 56698327 C T upstream_gene_variant MODIFIER c.-3569C>T| S1
S90
2 BAA09g57440 A09 56699435 G A upstream_gene_variant MODIFIER c.-2461G>A| S166
S68
3 BAA09g57440 A09 56699479 G A upstream_gene_variant MODIFIER c.-2417G>A| S42
4 BAA09g57440 A09 56699525 G A upstream_gene_variant MODIFIER c.-2371G>A| S38
5 BAA09g57440 A09 56699948 G A upstream_gene_variant MODIFIER c.-1948G>A| S231
6 BAA09g57440 A09 56700399 C T upstream_gene_variant MODIFIER c.-1497C>T| S229
7 BAA09g57440 A09 56700402 C T upstream_gene_variant MODIFIER c.-1494C>T| S108
8 BAA09g57440 A09 56700985 G A upstream_gene_variant MODIFIER c.-911G>A| S110
9 BAA09g57440 A09 56701330 C T upstream_gene_variant MODIFIER c.-566C>T| S50
10 BAA09g57440 A09 56702051 C T synonymous_variant LOW c.156C>T|p.Asn52Asn S28
11 BAA09g57440 A09 56703655 G A missense_variant MODERATE c.887G>A|p.Arg296His S39
12 BAA09g57440 A09 56703725 G A intron_variant MODIFIER c.914+43G>A| S82
S92
13 BAA09g57440 A09 56703763 C T intron_variant MODIFIER c.915-9C>T| S163
14 BAA09g57440 A09 56704149 C T missense_variant MODERATE c.1129C>T|p.Pro377Ser S100
15 BAA09g57440 A09 56704195 C T intron_variant MODIFIER c.1149+26C>T| S149
16 BAA09g57440 A09 56704710 G A missense_variant MODERATE c.1496G>A|p.Arg499Lys S221
17 BAA09g57440 A09 56704732 C T synonymous_variant LOW c.1518C>T|p.Asn506Asn S278
18 BAA09g57440 A09 56705164 C T synonymous_variant LOW c.1950C>T|p.Val650Val S18
19 BAA09g57440 A09 56707786 G A downstream_gene_variant MODIFIER c.*1998G>A| S48
20 BAA09g57440 A09 56708915 C T downstream_gene_variant MODIFIER c.*3127C>T| S278
21 BAA09g57440 A09 56709709 G A downstream_gene_variant MODIFIER c.*3921G>A| S37
22 BAA09g57440 A09 56710644 G A downstream_gene_variant MODIFIER c.*4856G>A| S32