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GCGGTCAACAGTGATAGCCAGCAAG[C/T]TGCAGACAGAGGCAGAGAAAGAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600752 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPR12 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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GPR12 - G protein-coupled receptor 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005288.3 | 611 | Missense Mutation | AAC,AGC | N,S 130 | NP_005279.1 | |
XM_005266360.3 | 611 | Intron | XP_005266417.1 |