Product Details

SNP ID

rs17588637

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:46279931 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAATTATCTAATGCATGAGTCATT[G/T]TCTTGCCCTACTGACCCTCTGGGGA

Phenotype

MIM: 616555

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

ARL17B PubMed Links

Additional Information

For this assay, SNP(s) [rs75033119] 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

ARL17B

Gene Name

ADP ribosylation factor like GTPase 17B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039083.3		Intron			NP_001034172.3
NM_001103154.1		Intron			NP_001096624.1
XM_005256918.4		Intron			XP_005256975.1
XM_011524160.2		Intron			XP_011522462.1
XM_011524161.2		Intron			XP_011522463.1
XM_011524162.2		Intron			XP_011522464.1
XM_011524163.2		Intron			XP_011522465.1
XM_011524164.2		Intron			XP_011522466.1
XM_011524165.2		Intron			XP_011522467.1
XM_011524166.2		Intron			XP_011522468.1
XM_011524167.2		Intron			XP_011522469.1

Gene

LRRC37A

Gene Name

leucine rich repeat containing 37A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014834.4		Intron			NP_055649.4
XM_005257879.4		Intron			XP_005257936.1
XM_005257880.4		Intron			XP_005257937.1
XM_005257882.4		Intron			XP_005257939.1
XM_005257883.4		Intron			XP_005257940.1
XM_005257884.4		Intron			XP_005257941.1
XM_006722210.3		Intron			XP_006722273.1
XM_006722211.3		Intron			XP_006722274.1
XM_011525539.2		Intron			XP_011523841.1
XM_017025472.1		Intron			XP_016880961.1
XM_017025473.1		Intron			XP_016880962.1

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