Product Details

SNP ID

rs6093966

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:44359432 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAGCAAAACTTCCCCAGAAACCT[C/T]CTGGCAGACTCCCCTAGTTCAAGGA

Phenotype

MIM: 600281

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HNF4A PubMed Links

Additional Information

For this assay, SNP(s) [rs60692239] 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

HNF4A

Gene Name

hepatocyte nuclear factor 4 alpha

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000457.4		Intron			NP_000448.3
NM_001030003.2		Intron			NP_001025174.1
NM_001030004.2		Intron			NP_001025175.1
NM_001258355.1		Intron			NP_001245284.1
NM_001287182.1		Intron			NP_001274111.1
NM_001287183.1		Intron			NP_001274112.1
NM_001287184.1		Intron			NP_001274113.1
NM_175914.4		Intron			NP_787110.2
NM_178849.2		Intron			NP_849180.1
NM_178850.2		Intron			NP_849181.1
XM_005260407.3		Intron			XP_005260464.1

Gene

R3HDML

Gene Name

R3H domain containing like

There are no transcripts associated with this gene.

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