Product Details

SNP ID

rs1023207

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.10:31805962 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACACGCTCACAACAACAAATACAGA[A/C]TTTCTACCACAAAATTCAGGTGAGA

Phenotype

MIM: 610577

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ARHGAP12 PubMed Links

Additional Information

For this assay, SNP(s) [rs12264870] 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

ARHGAP12

Gene Name

Rho GTPase activating protein 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270695.1	4319	UTR 3			NP_001257624.1
NM_001270696.1	4319	UTR 3			NP_001257625.1
NM_001270697.1	4319	UTR 3			NP_001257626.1
NM_001270698.1	4319	UTR 3			NP_001257627.1
NM_001270699.1	4319	UTR 3			NP_001257628.1
NM_018287.6	4319	UTR 3			NP_060757.4
XM_005252644.1	4319	UTR 3			XP_005252701.1
XM_011519761.1	4319	UTR 3			XP_011518063.1
XM_017016954.1	4319	UTR 3			XP_016872443.1

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