Product Details

SNP ID

rs1037831

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:75411094 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGGAAAAAGTGAACCAGAGAGAAAT[G/T]AAATAACTTGACTAAGGTTACACGT

Phenotype

MIM: 605966

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

HNF4G PubMed Links

Additional Information

For this assay, SNP(s) [rs78978135] 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

HNF4G

Gene Name

hepatocyte nuclear factor 4 gamma

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004133.4		Intron			NP_004124.4
XM_011517516.2		Intron			XP_011515818.1
XM_017013373.1		Intron			XP_016868862.1
XM_017013374.1		Intron			XP_016868863.1
XM_017013375.1		Intron			XP_016868864.1
XM_017013376.1		Intron			XP_016868865.1

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