Product Details

SNP ID

rs182719074

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:152410007 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTACAGTTTGGCTTCTGTCCTGCT[C/T]CACAGTCTCGGTGTGTGACCCTGCC

Phenotype

MIM: 611312

Polymorphism

C/T, Transition 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	1149	Missense Mutation	AAG,GAG	K359E	NP_057274.1

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