Product Details

SNP ID

rs10888486

Assay Type

Validated

NCBI dbSNP Submissions

55

Location

Chr.1:152409586 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTCTTCCAGTACTGGACATTGGAGT[C/T]GGGGAAGTCATGGCTTGGTGCTTCT

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	1570	UTR 3			NP_057274.1

View Full Product Details