Product Details

SNP ID

rs11186565

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:91423701 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAGTCTATTAATTCTAGAGACTT[C/T]TTAATTCTATGTGTATAGTGTCTGA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HECTD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs141441353] 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

HECTD2

Gene Name

HECT domain E3 ubiquitin protein ligase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284274.1		Intron			NP_001271203.1
NM_173497.3		Intron			NP_775768.3
NM_182765.4		Intron			NP_877497.3
XM_017015750.1		Intron			XP_016871239.1
XM_017015751.1		Intron			XP_016871240.1
XM_017015752.1		Intron			XP_016871241.1

Gene

HECTD2-AS1

Gene Name

HECTD2 antisense RNA 1

There are no transcripts associated with this gene.

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