Product Details

SNP ID

rs471933

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:100992623 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACACATTCACTGTATCCCTCATTGT[A/C]ACCGTTATCCCCCTGCTTCAAAATG

Phenotype

MIM: 615936

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ARHGAP42 PubMed Links

Additional Information

For this assay, SNP(s) [rs61995873] are located under a primer 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

ARHGAP42

Gene Name

Rho GTPase activating protein 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152432.2	544	Intron			NP_689645.2
XM_011542615.2	544	UTR 3			XP_011540917.1
XM_011542616.2	544	UTR 3			XP_011540918.1
XM_011542617.2	544	UTR 3			XP_011540919.1
XM_017017237.1	544	UTR 3			XP_016872726.1
XM_017017238.1	544	UTR 3			XP_016872727.1

Gene

TMEM133

Gene Name

transmembrane protein 133

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032021.2	544	Silent Mutation	GTA,GTC	V105V	NP_114410.1

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