Product Details

SNP ID

rs200067613

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:45856087 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCCGACGTGTTCCCAAGGCTGTT[C/G]AAGGTAAGCGTGCAGAGCCCCAGAG

Phenotype

MIM: 603732

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CRY2 PubMed Links

Gene Details

Gene

CRY2

Gene Name

cryptochrome circadian clock 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127457.2	406	Missense Mutation	TTC,TTG	F46L	NP_001120929.1
NM_021117.3	406	Missense Mutation	TTC,TTG	F128L	NP_066940.2

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