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TCTCATCTGCACCGGACAAGGAGGC[C/G]GGGAGGGAGCGCAGAGCACTCAGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607449 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NPFFR2 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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NPFFR2 - neuropeptide FF receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144756.1 | 179 | Intron | NP_001138228.1 | |||
NM_004885.2 | 179 | Silent Mutation | GCC,GCG | A,A 27 | NP_004876.2 | |
NM_053036.2 | 179 | Intron | NP_444264.1 | |||
XM_011531554.2 | 179 | Intron | XP_011529856.1 |