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 BAA09g33130 A09 41756605 G A upstream_gene_variant MODIFIER c.-4972G>A| S45
2 BAA09g33130 A09 41756712 C T upstream_gene_variant MODIFIER c.-4865C>T| S292
3 BAA09g33130 A09 41757287 C T upstream_gene_variant MODIFIER c.-4290C>T| S267
4 BAA09g33130 A09 41757313 G A upstream_gene_variant MODIFIER c.-4264G>A| S20
5 BAA09g33130 A09 41757336 G A upstream_gene_variant MODIFIER c.-4241G>A| S265
6 BAA09g33130 A09 41757872 C T upstream_gene_variant MODIFIER c.-3705C>T| S39
7 BAA09g33130 A09 41757965 C T upstream_gene_variant MODIFIER c.-3612C>T| S39
8 BAA09g33130 A09 41758501 G A upstream_gene_variant MODIFIER c.-3076G>A| S35
9 BAA09g33130 A09 41759061 G A upstream_gene_variant MODIFIER c.-2516G>A| S176
10 BAA09g33130 A09 41759094 C T upstream_gene_variant MODIFIER c.-2483C>T| S229
11 BAA09g33130 A09 41759247 C T upstream_gene_variant MODIFIER c.-2330C>T| S133
12 BAA09g33130 A09 41761598 G A missense_variant MODERATE c.22G>A|p.Gly8Ser S155
S211
13 BAA09g33130 A09 41761707 G A missense_variant MODERATE c.131G>A|p.Gly44Glu S38
14 BAA09g33130 A09 41761716 C T missense_variant MODERATE c.140C>T|p.Ser47Phe S174
15 BAA09g33130 A09 41762845 C T missense_variant MODERATE c.922C>T|p.Arg308Cys S210
16 BAA09g33130 A09 41762931 C T synonymous_variant LOW c.1008C>T|p.Pro336Pro S260
17 BAA09g33130 A09 41763624 G A missense_variant MODERATE c.1618G>A|p.Glu540Lys S15
S3
18 BAA09g33130 A09 41763900 C T downstream_gene_variant MODIFIER c.*25C>T| S245
S31
19 BAA09g33130 A09 41764352 C T downstream_gene_variant MODIFIER c.*477C>T| S132
S137
S215
S288
S89
20 BAA09g33130 A09 41765587 C T downstream_gene_variant MODIFIER c.*1712C>T| S278
21 BAA09g33130 A09 41765649 G A downstream_gene_variant MODIFIER c.*1774G>A| S13
22 BAA09g33130 A09 41766544 A T downstream_gene_variant MODIFIER c.*2669A>T| S202
23 BAA09g33130 A09 41768840 G A downstream_gene_variant MODIFIER c.*4965G>A| S62