Product Details

SNP ID

rs116018259

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:26540740 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATCTTCCCTCCAACCCCCAAACA[C/T]GATCTCTCCTTAAGTAAGAGGCAGG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HMGN4 PubMed Links

Gene Details

Gene

HMGN4

Gene Name

high mobility group nucleosomal binding domain 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006353.2		Intron			NP_006344.1
XM_017010171.1		Intron			XP_016865660.1
XM_017010172.1		Intron			XP_016865661.1
XM_017010173.1		Intron			XP_016865662.1

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