Product Details

SNP ID
rs187872798
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:24514415 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAATCTTGGAATGATAGCCAGTCA[C/G]ATCTGTGTAGCACTGACCAAGAAGA
Phenotype
MIM: 605860
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
RCAN3 PubMed Links

Gene Details

Gene
RCAN3
Gene Name
RCAN family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001251977.1 356 Missense Mutation CAT,GAT H15D NP_001238906.1
NM_001251978.1 356 Missense Mutation CAT,GAT H15D NP_001238907.1
NM_001251979.1 356 Missense Mutation CAT,GAT H15D NP_001238908.1
NM_001251980.1 356 Missense Mutation CAT,GAT H15D NP_001238909.1
NM_001251981.1 356 Missense Mutation CAT,GAT H15D NP_001238910.1
NM_001251982.1 356 Missense Mutation CAT,GAT H15D NP_001238911.1
NM_001251983.1 356 Intron NP_001238912.1
NM_001251984.1 356 Intron NP_001238913.1
NM_001251985.1 356 Missense Mutation CAT,GAT H15D NP_001238914.1
NM_013441.3 356 Missense Mutation CAT,GAT H15D NP_038469.1

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