Product Details

SNP ID

rs12406669

Assay Type

Functionally tested

NCBI dbSNP Submissions

33

Location

Chr.1:22065070 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTTTGCAGAGTGACTGACAACCT[C/G]TGATGGTGATACTATTGTCTCTGTT

Phenotype

MIM: 116952

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CDC42 PubMed Links

Gene Details

Gene

CDC42

Gene Name

cell division cycle 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039802.1		Intron			NP_001034891.1
NM_001791.3		Intron			NP_001782.1
NM_044472.2		Intron			NP_426359.1

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