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CTTCGTCTTCTGGCTGCTCTACTGC[C/T]TCCCTGTGTGCCTGCAGTTTTTCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 604658 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPR137B 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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GPR137B - G protein-coupled receptor 137B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003272.3 | 449 | Missense Mutation | CTC,TTC | L,F 120 | NP_003263.1 | |
XM_017002209.1 | 449 | Missense Mutation | CTC,TTC | L,F 120 | XP_016857698.1 | |
XM_017002210.1 | 449 | Missense Mutation | CTC,TTC | L,F 120 | XP_016857699.1 |