Product Details

SNP ID

rs113361561

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75012705 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGAGCATGGCGGCCACCAGGTGC[C/T]TGCGCTGGGGCCTGAGCCGAGCCGG

Phenotype

MIM: 603000

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CDR2L PubMed Links

Additional Information

For this assay, SNP(s) [rs3744206] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

CDR2L

Gene Name

cerebellar degeneration related protein 2 like

There are no transcripts associated with this gene.

Gene

MRPL58

Gene Name

mitochondrial ribosomal protein L58

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303265.1	42	Silent Mutation	CTG,TTG	L7L	NP_001290194.1
NM_001545.2	42	Silent Mutation	CTG,TTG	L7L	NP_001536.1
XM_017024574.1	42	Intron			XP_016880063.1

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