Product Details

SNP ID

rs11786734

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:123646164 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTCTGAACTAGCACGTGGGATGTTG[A/G]GCTAACCTGCCAAGGCCTGCTTTGT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

KLHL38 PubMed Links

Additional Information

For this assay, SNP(s) [rs77201406] 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

KLHL38

Gene Name

kelch like family member 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001081675.2		Intron			NP_001075144.2
XM_005250901.4		Intron			XP_005250958.1

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