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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g08210 A05 4081416 C T upstream_gene_variant MODIFIER c.-4663C>T| S39
2 BAA05g08210 A05 4081655 C T upstream_gene_variant MODIFIER c.-4424C>T| S130
3 BAA05g08210 A05 4081697 C T upstream_gene_variant MODIFIER c.-4382C>T| S140
4 BAA05g08210 A05 4082357 C T upstream_gene_variant MODIFIER c.-3722C>T| S295
5 BAA05g08210 A05 4082549 G A upstream_gene_variant MODIFIER c.-3530G>A| S278
6 BAA05g08210 A05 4082858 C T upstream_gene_variant MODIFIER c.-3221C>T| S10
7 BAA05g08210 A05 4082984 C T upstream_gene_variant MODIFIER c.-3095C>T| S269
8 BAA05g08210 A05 4083404 C T upstream_gene_variant MODIFIER c.-2675C>T| S118
9 BAA05g08210 A05 4084054 G A upstream_gene_variant MODIFIER c.-2025G>A| S204
10 BAA05g08210 A05 4084121 C T upstream_gene_variant MODIFIER c.-1958C>T| S261
11 BAA05g08210 A05 4084721 C T upstream_gene_variant MODIFIER c.-1358C>T| S237
12 BAA05g08210 A05 4085725 C T upstream_gene_variant MODIFIER c.-354C>T| S207
13 BAA05g08210 A05 4086192 G A synonymous_variant LOW c.114G>A|p.Gln38Gln S15
S3
14 BAA05g08210 A05 4086450 C T missense_variant MODERATE c.221C>T|p.Ala74Val S61
15 BAA05g08210 A05 4086490 C T synonymous_variant LOW c.261C>T|p.Gly87Gly S265
16 BAA05g08210 A05 4088320 C T downstream_gene_variant MODIFIER c.*494C>T| S266
17 BAA05g08210 A05 4088871 G A downstream_gene_variant MODIFIER c.*1045G>A| S133