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AGCCTGTACTGCCTGGCCAGGCACA[C/G]CTCCTCCTGCCGCTGCCTTACAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609044 MIM: 180250 | ||||||||||||||||||||
Literature Links: |
FFAR4 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 |
FFAR4 - free fatty acid receptor 4 | ||||||
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There are no transcripts associated with this gene. |
RBP4 - retinol binding protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323517.1 | 613 | Missense Mutation | CTG,GTG | L,V 177 | NP_001310446.1 | |
NM_001323518.1 | 613 | Missense Mutation | CTG,GTG | L,V 175 | NP_001310447.1 | |
NM_006744.3 | 613 | Missense Mutation | CTG,GTG | L,V 177 | NP_006735.2 |