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GCTCGGTGGACACGCTGCCCCGCAC[A/G]GCCCGCAGGATGCCCCGGTACGACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600551 MIM: 606580 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPR4 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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GPR4 - G protein-coupled receptor 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005282.2 | 2154 | Silent Mutation | GCC,GCT | A,A 207 | NP_005273.1 | |
XM_017026607.1 | 2154 | Silent Mutation | GCC,GCT | A,A 207 | XP_016882096.1 | |
XM_017026608.1 | 2154 | Silent Mutation | GCC,GCT | A,A 207 | XP_016882097.1 |
OPA3 - optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) | ||||||
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There are no transcripts associated with this gene. |