Product Details

SNP ID

rs9501871

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:2667263 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACAGAATCAGCTACATGGAAGAAAA[C/T]GCACGCTGGGGACAATTCAGAATAA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYLK4 PubMed Links

Additional Information

For this assay, SNP(s) [rs9501872] 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

MYLK4

Gene Name

myosin light chain kinase family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005249078.3	2023	UTR 3			XP_005249135.2
XM_005249079.2	2023	UTR 3			XP_005249136.1
XM_006715082.3	2023	UTR 3			XP_006715145.1
XM_011514567.2	2023	UTR 3			XP_011512869.1
XM_017010819.1	2023	UTR 3			XP_016866308.1

View Full Product Details