Product Details

SNP ID

rs7679833

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:85476523 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTTGGAATATAAAAGTTGTTAAGG[C/T]TTTGCTTATACATAAATACATAAAT

Phenotype

MIM: 610586

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ARHGAP24 PubMed Links

Additional Information

For this assay, SNP(s) [rs188746600,rs57577827] 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

ARHGAP24

Gene Name

Rho GTPase activating protein 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025616.2		Intron			NP_001020787.2
NM_001042669.1		Intron			NP_001036134.1
NM_001287805.1		Intron			NP_001274734.1
NM_031305.2		Intron			NP_112595.2
XM_011532300.2		Intron			XP_011530602.1
XM_017008679.1		Intron			XP_016864168.1

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