Product Details

SNP ID

rs443816

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:34622936 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTGCTGTAAGTTCTCTTACATGAC[C/T]GCGCAAGATGGTAGCCTTCATCAAG

Phenotype

MIM: 605439

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EHF PubMed Links

Additional Information

For this assay, SNP(s) [rs77566387] 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

EHF

Gene Name

ETS homologous factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206615.1		Intron			NP_001193544.1
NM_001206616.1		Intron			NP_001193545.1
NM_012153.5		Intron			NP_036285.2
XM_005252857.1		Intron			XP_005252914.1
XM_005252860.1		Intron			XP_005252917.1
XM_005252861.1		Intron			XP_005252918.1
XM_005252862.1		Intron			XP_005252919.1
XM_011519983.1		Intron			XP_011518285.1
XM_011519984.1		Intron			XP_011518286.1
XM_011519985.1		Intron			XP_011518287.1
XM_017017534.1		Intron			XP_016873023.1

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