Product Details

SNP ID

rs143697299

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:55267809 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGATGATGAGAGTAACAGCCCGAC[A/G]GTCCCCCAGTCGGCATTCCTGGGGC

Phenotype

MIM: 142385

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HLF PubMed Links

Gene Details

Gene

HLF

Gene Name

HLF, PAR bZIP transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002126.4	153	Silent Mutation	ACA,ACG	T58T	NP_002117.1
XM_005257269.2	153	Silent Mutation	ACA,ACG	T58T	XP_005257326.1
XM_011524705.1	153	UTR 5			XP_011523007.1
XM_017024556.1	153	UTR 5			XP_016880045.1

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