Product Details

SNP ID

rs11084798

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:35047644 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTCCCGGAACCTAGAAAGGTGCCA[A/G]GCACACAGCGGATGTTCAGTAGGAT

Phenotype

MIM: 142440 MIM: 600235

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HPN PubMed Links

Additional Information

For this assay, SNP(s) [rs10690630,rs11392434] 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

HPN

Gene Name

hepsin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002151.2		Intron			NP_002142.1
NM_182983.2		Intron			NP_892028.1
XM_005258838.4		Intron			XP_005258895.2
XM_006723181.3		Intron			XP_006723244.2
XM_017026731.1		Intron			XP_016882220.1
XM_017026732.1		Intron			XP_016882221.1

Gene

SCN1B

Gene Name

sodium voltage-gated channel beta subunit 1

There are no transcripts associated with this gene.

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