Product Details

SNP ID

rs4789124

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:74999282 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTATTTTTGTTTGTTTTTTATTA[A/C]ATCTTGCACACACACACACACACAC

Phenotype

Polymorphism

A/C, Transversion 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		Intron			NP_055418.2
XM_006721852.2		Intron			XP_006721915.1

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