Product Details

SNP ID
rs1801197
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.7:93426441 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TTGGTTGTTGGCTGGTTCATTCCTC[A/G]GCTCCTGATGGCAGATGTAAATTGG
Phenotype
MIM: 114131
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CALCR PubMed Links

Gene Details

Gene
CALCR
Gene Name
calcitonin receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001164737.1 1623 Missense Mutation CCG,CTG P481L NP_001158209.1
NM_001164738.1 1623 Missense Mutation CCG,CTG P447L NP_001158210.1
NM_001742.3 1623 Missense Mutation CCG,CTG P447L NP_001733.1

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