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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g40930 A09 47831209 G A downstream_gene_variant MODIFIER c.*2850C>T| S274
2 BAA09g40930 A09 47831642 G A downstream_gene_variant MODIFIER c.*2417C>T| S266
3 BAA09g40930 A09 47831823 G A downstream_gene_variant MODIFIER c.*2236C>T| S111
4 BAA09g40930 A09 47832894 G A downstream_gene_variant MODIFIER c.*1165C>T| S249
5 BAA09g40930 A09 47833293 G A downstream_gene_variant MODIFIER c.*766C>T| S181
6 BAA09g40930 A09 47833384 G A downstream_gene_variant MODIFIER c.*675C>T| S129
7 BAA09g40930 A09 47833739 C T downstream_gene_variant MODIFIER c.*320G>A| S60
8 BAA09g40930 A09 47833792 G A downstream_gene_variant MODIFIER c.*267C>T| S87
9 BAA09g40930 A09 47833995 G A downstream_gene_variant MODIFIER c.*64C>T| S305
10 BAA09g40930 A09 47834133 G A missense_variant MODERATE c.2695C>T|p.Pro899Ser S81
S85
11 BAA09g40930 A09 47834445 G A missense_variant MODERATE c.2383C>T|p.Pro795Ser S207
12 BAA09g40930 A09 47835090 G A missense_variant MODERATE c.1738C>T|p.Pro580Ser S172
S217
13 BAA09g40930 A09 47835195 G A missense_variant MODERATE c.1633C>T|p.Pro545Ser S144
14 BAA09g40930 A09 47835404 G A missense_variant MODERATE c.1424C>T|p.Ala475Val S59
15 BAA09g40930 A09 47835516 G A missense_variant MODERATE c.1312C>T|p.Pro438Ser S162
16 BAA09g40930 A09 47836512 G A missense_variant MODERATE c.316C>T|p.Pro106Ser S308
17 BAA09g40930 A09 47836551 G A missense_variant MODERATE c.277C>T|p.Pro93Ser S42
18 BAA09g40930 A09 47837749 G A upstream_gene_variant MODIFIER c.-922C>T| S244
19 BAA09g40930 A09 47837798 G A upstream_gene_variant MODIFIER c.-971C>T| S209
20 BAA09g40930 A09 47838867 C T upstream_gene_variant MODIFIER c.-2040G>A| S182
21 BAA09g40930 A09 47838936 G A upstream_gene_variant MODIFIER c.-2109C>T| S273
22 BAA09g40930 A09 47838961 C T upstream_gene_variant MODIFIER c.-2134G>A| S122
23 BAA09g40930 A09 47839635 G A upstream_gene_variant MODIFIER c.-2808C>T| S88