Product Details

SNP ID

rs9998858

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:73077741 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCTAAAAACTTGGTGTTATAAAAC[A/G]AAAGAAAAAAACCTAAGTACAACCT

Phenotype

MIM: 615929 MIM: 610428

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ANKRD17 PubMed Links

Additional Information

For this assay, SNP(s) [rs141699723] 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

ANKRD17

Gene Name

ankyrin repeat domain 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286771.2		Intron			NP_001273700.1
NM_015574.1		Intron			NP_056389.1
NM_032217.4		Intron			NP_115593.3
NM_198889.2		Intron			NP_942592.1
XM_005265671.3		Intron			XP_005265728.1
XM_005265672.3		Intron			XP_005265729.1
XM_005265673.3		Intron			XP_005265730.1
XM_017008011.1		Intron			XP_016863500.1
XM_017008012.1		Intron			XP_016863501.1
XM_017008013.1		Intron			XP_016863502.1
XM_017008014.1		Intron			XP_016863503.1
XM_017008015.1		Intron			XP_016863504.1
XM_017008016.1		Intron			XP_016863505.1
XM_017008017.1		Intron			XP_016863506.1

Gene

COX18

Gene Name

COX18, cytochrome c oxidase assembly factor

There are no transcripts associated with this gene.

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