Product Details

SNP ID
rs142173136
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:81119810 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCTCCTGCCTCATATCACCTTGA[A/C]CTGCAGCCTACACAGAGGAGAAAAC
Phenotype
MIM: 300385
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
HMGN5 PubMed Links

Gene Details

Gene
HMGN5
Gene Name
high mobility group nucleosome binding domain 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030763.2 299 Missense Mutation GGT,GTT G8V NP_110390.1
XM_006724688.3 299 Missense Mutation GGT,GTT G8V XP_006724751.1
XM_017029839.1 299 Intron XP_016885328.1
XM_017029840.1 299 Intron XP_016885329.1

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