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AAAAGATGACTCAGTAAAATGTTAG[G/T]ATCTTGTCCAGAGAAATCCTGAAAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
15 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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 289 | Missense Mutation | ACT,CCT | T,P 95 | NP_006777.1 | |
NM_021995.2 | 289 | Missense Mutation | ACT,CCT | T,P 110 | NP_068835.1 | |
XM_011540537.2 | 289 | Missense Mutation | ACT,CCT | T,P 110 | XP_011538839.1 | |
XM_011540538.1 | 289 | Missense Mutation | ACT,CCT | T,P 95 | XP_011538840.1 | |
XM_017000116.1 | 289 | Missense Mutation | ACT,CCT | T,P 110 | XP_016855605.1 | |
XM_017000117.1 | 289 | Missense Mutation | ACT,CCT | T,P 95 | XP_016855606.1 | |
XM_017000118.1 | 289 | Missense Mutation | ACT,CCT | T,P 65 | XP_016855607.1 | |
XM_017000119.1 | 289 | Intron | XP_016855608.1 |