Product Details

SNP ID
rs141389663
Assay Type
Functionally tested
NCBI dbSNP Submissions
12
Location
Chr.1:7850874 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCTCTGGCAGTATCTGTAGAAGG[A/G]AAGCTCTTTCTAGCTCCTCCGGAGT
Phenotype
MIM: 603427 MIM: 604097
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PER3 PubMed Links

Gene Details

Gene
PER3
Gene Name
period circadian clock 3
There are no transcripts associated with this gene.

Gene
UTS2
Gene Name
urotensin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006786.3 706 Missense Mutation TCC,TTC S51F NP_006777.1
NM_021995.2 706 Missense Mutation TCC,TTC S66F NP_068835.1
XM_011540537.2 706 Missense Mutation TCC,TTC S66F XP_011538839.1
XM_011540538.1 706 Missense Mutation TCC,TTC S51F XP_011538840.1
XM_017000116.1 706 Missense Mutation TCC,TTC S66F XP_016855605.1
XM_017000117.1 706 Missense Mutation TCC,TTC S51F XP_016855606.1
XM_017000118.1 706 Missense Mutation TCC,TTC S21F XP_016855607.1
XM_017000119.1 706 Missense Mutation TCC,TTC S66F XP_016855608.1

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