Product Details

SNP ID

rs6956444

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:130089132 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATGTACAGTAAAAAAAAAACATAT[A/G]TTTTAAAATGAACTTTTATCTTTTA

Phenotype

MIM: 615152

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

KLHDC10 PubMed Links

Additional Information

For this assay, SNP(s) [rs114198699] 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

KLHDC10

Gene Name

kelch domain containing 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014997.3		Intron			NP_055812.1
XM_005250233.4		Intron			XP_005250290.1

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