Product Details

SNP ID

rs200365440

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75001341 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTACTCAATGTCCTTCCACCCCCAG[C/T]ACCTAACCAAGCAGCTGGACACGCT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CDR2L PubMed Links

Gene Details

Gene

CDR2L

Gene Name

cerebellar degeneration related protein 2 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014603.2	590	Missense Mutation	CAC,TAC	H65Y	NP_055418.2
XM_006721852.2	590	Missense Mutation	CAC,TAC	H65Y	XP_006721915.1

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