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 BAA05g09900 A05 5050846 C T upstream_gene_variant MODIFIER c.-4950C>T| S269
2 BAA05g09900 A05 5051298 C T upstream_gene_variant MODIFIER c.-4498C>T| S193
3 BAA05g09900 A05 5051680 C T upstream_gene_variant MODIFIER c.-4116C>T| S12
4 BAA05g09900 A05 5051963 C T upstream_gene_variant MODIFIER c.-3833C>T| S278
5 BAA05g09900 A05 5051995 G A upstream_gene_variant MODIFIER c.-3801G>A| S158
6 BAA05g09900 A05 5052534 C T upstream_gene_variant MODIFIER c.-3262C>T| S197
7 BAA05g09900 A05 5052822 C T upstream_gene_variant MODIFIER c.-2974C>T| S163
8 BAA05g09900 A05 5053878 C T upstream_gene_variant MODIFIER c.-1918C>T| S267
9 BAA05g09900 A05 5054639 G A upstream_gene_variant MODIFIER c.-1157G>A| S62
10 BAA05g09900 A05 5055520 C T upstream_gene_variant MODIFIER c.-276C>T| S19
11 BAA05g09900 A05 5056427 C T missense_variant MODERATE c.632C>T|p.Ser211Phe S303
12 BAA05g09900 A05 5057016 C T missense_variant MODERATE c.689C>T|p.Ala230Val S130
13 BAA05g09900 A05 5057039 G A missense_variant MODERATE c.712G>A|p.Ala238Thr S269
14 BAA05g09900 A05 5057048 G A missense_variant MODERATE c.721G>A|p.Val241Ile S238
15 BAA05g09900 A05 5057695 G A synonymous_variant LOW c.1368G>A|p.Gln456Gln S257
16 BAA05g09900 A05 5057778 C T missense_variant MODERATE c.1451C>T|p.Ser484Phe S229
17 BAA05g09900 A05 5057873 A T missense_variant MODERATE c.1546A>T|p.Ser516Cys S107
18 BAA05g09900 A05 5057991 G A missense_variant MODERATE c.1664G>A|p.Gly555Glu S210
S225
19 BAA05g09900 A05 5058096 C T missense_variant MODERATE c.1769C>T|p.Ser590Phe S193
20 BAA05g09900 A05 5058207 C T missense_variant MODERATE c.1802C>T|p.Ser601Phe S268
21 BAA05g09900 A05 5058209 C T missense_variant MODERATE c.1804C>T|p.His602Tyr S108
22 BAA05g09900 A05 5058518 G A missense_variant MODERATE c.2113G>A|p.Gly705Ser S238
23 BAA05g09900 A05 5058823 G A downstream_gene_variant MODIFIER c.*177G>A| S161