Product Details

SNP ID

rs200866893

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:146116949 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTGTCAGCAGCTGCCTCTGCAGA[A/G]CCTGGACGGCTCCCTCCACGTCCCG

Phenotype

MIM: 604569

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CNTNAP2 PubMed Links

Gene Details

Gene

CNTNAP2

Gene Name

contactin associated protein-like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014141.5	915	Missense Mutation	ACC,GCC	T25A	NP_054860.1
XM_017011950.1	915	Missense Mutation	ACC,GCC	T25A	XP_016867439.1

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