Product Details

SNP ID
rs150002541
Assay Type
Functionally Tested
NCBI dbSNP Submissions
5
Location
Chr.1:152409811 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCTCCCTGCCCTTCTGTCACACAG[C/G]GCCTTGGGTGAGTGCTGCTCCACTC
Phenotype
MIM: 611312
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
CRNN PubMed Links

Gene Details

Gene
CRNN
Gene Name
cornulin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016190.2 1345 Missense Mutation CCC,CGC P424R NP_057274.1

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