Product Details

SNP ID

rs991435

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:86248322 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTGGGAGGAGATGGGTAAATTAAGT[C/G]ATCAGAAGTAAAATAAGCAACGTGC

Phenotype

MIM: 605984

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

EED PubMed Links

Additional Information

For this assay, SNP(s) [rs78592973] 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

EED

Gene Name

embryonic ectoderm development

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308007.1		Intron			NP_001294936.1
NM_003797.4		Intron			NP_003788.2
XM_005274373.2		Intron			XP_005274430.1
XM_011545330.1		Intron			XP_011543632.1
XM_011545331.1		Intron			XP_011543633.1
XM_017018512.1		Intron			XP_016874001.1
XM_017018513.1		Intron			XP_016874002.1

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