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TTTTTCAGGAAGGATGCCAATTCTG[C/T]GCTTCTCAGTAACTACGAGGTAAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606121 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CRCP 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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CRCP - CGRP receptor component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040647.1 | 171 | Missense Mutation | GCG,GTG | A,V 9 | NP_001035737.1 | |
NM_001040648.1 | 171 | Intron | NP_001035738.1 | |||
NM_001142414.1 | 171 | Missense Mutation | GCG,GTG | A,V 35 | NP_001135886.1 | |
NM_014478.4 | 171 | Missense Mutation | GCG,GTG | A,V 9 | NP_055293.1 |