Product Details

SNP ID

rs17010737

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:124028360 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATTTACATTTCTCATAATCTGACC[A/G]AAACCTGGGCTTTTAACTTCAAAGG

Phenotype

MIM: 610519

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CNTNAP5 PubMed Links

Gene Details

Gene

CNTNAP5

Gene Name

contactin associated protein like 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_130773.3		Intron			NP_570129.1
XM_006712258.1		Intron			XP_006712321.1
XM_017003316.1		Intron			XP_016858805.1

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