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 BAA09g35470 A09 43843091 C T downstream_gene_variant MODIFIER c.*2329G>A| S104
S52
2 BAA09g35470 A09 43843430 G A downstream_gene_variant MODIFIER c.*1990C>T| S132
S137
S215
3 BAA09g35470 A09 43843498 C T downstream_gene_variant MODIFIER c.*1922G>A| S235
4 BAA09g35470 A09 43843574 G A downstream_gene_variant MODIFIER c.*1846C>T| S174
S216
S27
S39
5 BAA09g35470 A09 43843964 C T downstream_gene_variant MODIFIER c.*1456G>A| S25
S264
6 BAA09g35470 A09 43844008 C T downstream_gene_variant MODIFIER c.*1412G>A| S77
S82
7 BAA09g35470 A09 43844338 G A downstream_gene_variant MODIFIER c.*1082C>T| S17
8 BAA09g35470 A09 43844376 G A downstream_gene_variant MODIFIER c.*1044C>T| S295
9 BAA09g35470 A09 43844929 C T downstream_gene_variant MODIFIER c.*491G>A| S278
10 BAA09g35470 A09 43845554 G A missense_variant MODERATE c.1459C>T|p.Arg487Trp S143
11 BAA09g35470 A09 43845557 C T missense_variant MODERATE c.1456G>A|p.Val486Ile S143
12 BAA09g35470 A09 43845609 C T synonymous_variant LOW c.1404G>A|p.Ser468Ser S32
13 BAA09g35470 A09 43845755 G A missense_variant MODERATE c.1258C>T|p.Pro420Ser S138
14 BAA09g35470 A09 43846338 G A synonymous_variant LOW c.675C>T|p.Leu225Leu S57
15 BAA09g35470 A09 43846628 G A synonymous_variant LOW c.627C>T|p.Val209Val S99
16 BAA09g35470 A09 43847581 G A upstream_gene_variant MODIFIER c.-327C>T| S98
17 BAA09g35470 A09 43848342 G A upstream_gene_variant MODIFIER c.-1088C>T| S62
18 BAA09g35470 A09 43849283 C T upstream_gene_variant MODIFIER c.-2029G>A| S246
19 BAA09g35470 A09 43849326 G A upstream_gene_variant MODIFIER c.-2072C>T| S281
20 BAA09g35470 A09 43850381 G A upstream_gene_variant MODIFIER c.-3127C>T| S201
21 BAA09g35470 A09 43850549 G A upstream_gene_variant MODIFIER c.-3295C>T| S71
22 BAA09g35470 A09 43850757 G A upstream_gene_variant MODIFIER c.-3503C>T| S235
23 BAA09g35470 A09 43851960 G A upstream_gene_variant MODIFIER c.-4706C>T| S42