Product Details

SNP ID
rs200609248
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:26545328 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCCTCCAAAACCAGAGCCCAGGC[C/G]TAAAAAGGCCTCTGCAAAGAAGGGA
Phenotype
Polymorphism
C/G, 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_006353.2 360 Missense Mutation CCT,CGT P41R NP_006344.1
XM_017010171.1 360 Missense Mutation CCT,CGT P41R XP_016865660.1
XM_017010172.1 360 Missense Mutation CCT,CGT P41R XP_016865661.1
XM_017010173.1 360 Missense Mutation CCT,CGT P41R XP_016865662.1

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