Product Details

SNP ID

rs17138512

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:37686595 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTACTCTGACACACTACATTCAGC[C/T]CCTCCAGGGATCCAGAGGTGTGTCT

Phenotype

MIM: 189907

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HNF1B PubMed Links

Additional Information

For this assay, SNP(s) [rs75361710] 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

HNF1B

Gene Name

HNF1 homeobox B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000458.3	2429	UTR 3			NP_000449.1
NM_001165923.3	2429	UTR 3			NP_001159395.1
NM_001304286.1	2429	UTR 3			NP_001291215.1
XM_011525160.1	2429	UTR 3			XP_011523462.1
XM_011525161.1	2429	UTR 3			XP_011523463.1
XM_011525162.2	2429	Intron			XP_011523464.1
XM_011525163.2	2429	Intron			XP_011523465.1
XM_011525164.1	2429	UTR 3			XP_011523466.1

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