Product Details

SNP ID

rs56014870

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:183638503 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATAAATATTTGGGTATGGACTGTA[G/T]AATGGAAAAATGTAAGTAAATATCT

Phenotype

MIM: 611295

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

KLHL24 PubMed Links

Additional Information

For this assay, SNP(s) [rs139128155] 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

KLHL24

Gene Name

kelch like family member 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017644.3		Intron			NP_060114.2
XM_005247552.2		Intron			XP_005247609.1
XM_005247553.1		Intron			XP_005247610.1
XM_005247554.2		Intron			XP_005247611.1
XM_005247555.1		Intron			XP_005247612.1
XM_005247556.1		Intron			XP_005247613.1
XM_011512938.2		Intron			XP_011511240.1
XM_017006650.1		Intron			XP_016862139.1
XM_017006651.1		Intron			XP_016862140.1
XM_017006652.1		Intron			XP_016862141.1
XM_017006653.1		Intron			XP_016862142.1
XM_017006654.1		Intron			XP_016862143.1
XM_017006655.1		Intron			XP_016862144.1
XM_017006656.1		Intron			XP_016862145.1
XM_017006657.1		Intron			XP_016862146.1
XM_017006658.1		Intron			XP_016862147.1
XM_017006659.1		Intron			XP_016862148.1
XM_017006660.1		Intron			XP_016862149.1
XM_017006661.1		Intron			XP_016862150.1
XM_017006662.1		Intron			XP_016862151.1
XM_017006663.1		Intron			XP_016862152.1

View Full Product Details