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 BAA09g51140 A09 53640115 C T downstream_gene_variant MODIFIER c.*4918G>A| S306
S308
2 BAA09g51140 A09 53640946 G A downstream_gene_variant MODIFIER c.*4087C>T| S144
3 BAA09g51140 A09 53641232 C T downstream_gene_variant MODIFIER c.*3801G>A| S45
4 BAA09g51140 A09 53641634 C T downstream_gene_variant MODIFIER c.*3399G>A| S25
5 BAA09g51140 A09 53642042 G A downstream_gene_variant MODIFIER c.*2991C>T| S262
6 BAA09g51140 A09 53642394 C T downstream_gene_variant MODIFIER c.*2639G>A| S109
7 BAA09g51140 A09 53642465 C T downstream_gene_variant MODIFIER c.*2568G>A| S205
8 BAA09g51140 A09 53642786 C T downstream_gene_variant MODIFIER c.*2247G>A| S242
9 BAA09g51140 A09 53642855 C T downstream_gene_variant MODIFIER c.*2178G>A| S108
10 BAA09g51140 A09 53643413 C T downstream_gene_variant MODIFIER c.*1620G>A| S208
S93
11 BAA09g51140 A09 53643448 C T downstream_gene_variant MODIFIER c.*1585G>A| S212
12 BAA09g51140 A09 53643488 C T downstream_gene_variant MODIFIER c.*1545G>A| S256
13 BAA09g51140 A09 53643691 C T downstream_gene_variant MODIFIER c.*1342G>A| S204
S43
14 BAA09g51140 A09 53644094 C T downstream_gene_variant MODIFIER c.*939G>A| S149
S176
15 BAA09g51140 A09 53644165 C T downstream_gene_variant MODIFIER c.*868G>A| S116
16 BAA09g51140 A09 53644191 G A downstream_gene_variant MODIFIER c.*842C>T| S155
S211
17 BAA09g51140 A09 53644663 C T downstream_gene_variant MODIFIER c.*370G>A| S255
18 BAA09g51140 A09 53644715 G A downstream_gene_variant MODIFIER c.*318C>T| S216
19 BAA09g51140 A09 53645206 C T missense_variant MODERATE c.157G>A|p.Ala53Thr S245
20 BAA09g51140 A09 53645469 G A upstream_gene_variant MODIFIER c.-107C>T| S187
21 BAA09g51140 A09 53648222 C T upstream_gene_variant MODIFIER c.-2860G>A| S33
22 BAA09g51140 A09 53649880 C T upstream_gene_variant MODIFIER c.-4518G>A| S183
23 BAA09g51140 A09 53649938 C T upstream_gene_variant MODIFIER c.-4576G>A| S164