Product Details

SNP ID

rs114496022

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:26542924 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGAAAAGAGACTGTGTGAGCATT[C/T]TCACACCAGGAAATGGGCTGAGAAA

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	163	Intron			NP_006344.1
XM_017010171.1	163	UTR 5			XP_016865660.1
XM_017010172.1	163	Intron			XP_016865661.1
XM_017010173.1	163	UTR 5			XP_016865662.1

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