Product Details

SNP ID

rs2905455

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:45395737 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCCCCCTTCCCGCGCGGGCCGCCC[A/G]GCTCACCGGCAGAGGTGCTGGAAGA

Phenotype

MIM: 610591

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ARHGAP27 PubMed Links

Additional Information

For this assay, SNP(s) [rs188239464] are located under a probe 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

ARHGAP27

Gene Name

Rho GTPase activating protein 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282290.1		Intron			NP_001269219.1
NM_174919.3		Intron			NP_777579.2
NM_199282.2		Intron			NP_954976.1
XM_005257128.3		Intron			XP_005257185.1
XM_006721745.2		Intron			XP_006721808.1
XM_006721747.2		Intron			XP_006721810.1
XM_006721750.3		Intron			XP_006721813.1
XM_011524468.1		Intron			XP_011522770.1
XM_011524469.1		Intron			XP_011522771.1
XM_011524470.2		Intron			XP_011522772.1
XM_011524471.1		Intron			XP_011522773.1
XM_011524472.2		Intron			XP_011522774.1
XM_011524473.2		Intron			XP_011522775.1
XM_011524474.1		Intron			XP_011522776.1
XM_017024311.1		Intron			XP_016879800.1
XM_017024312.1		Intron			XP_016879801.1
XM_017024313.1		Intron			XP_016879802.1

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