Product Details

SNP ID

rs150488159

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:65320948 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGAAGCGTGGCAGTCGCAAGGGCA[A/G]GAAGGAGAAGCTTCGGGACCTGCTG

Phenotype

MIM: 606132

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CDC42EP2 PubMed Links

Gene Details

Gene

CDC42EP2

Gene Name

CDC42 effector protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006779.3	653	Missense Mutation	AAG,AGG	K17R	NP_006770.1
XM_017017094.1	653	Missense Mutation	AAG,AGG	K17R	XP_016872583.1

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