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CATCTCTGGCAGTATCTGTAGAAGG[A/G]AAGCTCTTTCTAGCTCCTCCGGAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 603427 MIM: 604097 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PER3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PER3 - period circadian clock 3 | ||||||
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There are no transcripts associated with this gene. |
UTS2 - urotensin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006786.3 | 706 | Missense Mutation | TCC,TTC | S,F 51 | NP_006777.1 | |
NM_021995.2 | 706 | Missense Mutation | TCC,TTC | S,F 66 | NP_068835.1 | |
XM_011540537.2 | 706 | Missense Mutation | TCC,TTC | S,F 66 | XP_011538839.1 | |
XM_011540538.1 | 706 | Missense Mutation | TCC,TTC | S,F 51 | XP_011538840.1 | |
XM_017000116.1 | 706 | Missense Mutation | TCC,TTC | S,F 66 | XP_016855605.1 | |
XM_017000117.1 | 706 | Missense Mutation | TCC,TTC | S,F 51 | XP_016855606.1 | |
XM_017000118.1 | 706 | Missense Mutation | TCC,TTC | S,F 21 | XP_016855607.1 | |
XM_017000119.1 | 706 | Missense Mutation | TCC,TTC | S,F 66 | XP_016855608.1 |