Product Details

SNP ID

rs11878940

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:50191914 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGAAGGCAGAGTGAAAAGGAAGG[C/G]CCTGGTCAAGGGAAATATTACCCTC

Phenotype

MIM: 608568

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

MYH14 PubMed Links

Additional Information

For this assay, SNP(s) [rs79250592] 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

MYH14

Gene Name

myosin, heavy chain 14, non-muscle

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077186.1		Intron			NP_001070654.1
NM_001145809.1		Intron			NP_001139281.1
NM_024729.3		Intron			NP_079005.3
XM_006723386.3		Intron			XP_006723449.1
XM_011527320.2		Intron			XP_011525622.1
XM_011527321.2		Intron			XP_011525623.1
XM_011527323.2		Intron			XP_011525625.1

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