Product Details

SNP ID

rs6932865

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:26539938 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

GTTATTATGGTGCCCAGAAAGGGGG[A/C]AAAGGTTCCAGGGTCCTAGGAGATG

Phenotype

Polymorphism

A/C, Transversion 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	193	Intron			NP_006344.1
XM_017010171.1	193	Intron			XP_016865660.1
XM_017010172.1	193	UTR 5			XP_016865661.1
XM_017010173.1	193	Intron			XP_016865662.1

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