Product Details

SNP ID
rs148090107
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:81116269 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGTCTTCTTCAACAACTGCTTCTT[G/T]CTTGGTTTCAGCAACTGCTTGGGCA
Phenotype
MIM: 300385
Polymorphism
G/T, 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_030763.2 361 Missense Mutation AAA,CAA K68Q NP_110390.1
XM_006724688.3 361 Missense Mutation AAA,CAA K69Q XP_006724751.1
XM_017029839.1 361 Missense Mutation AAA,CAA K59Q XP_016885328.1
XM_017029840.1 361 Missense Mutation AAA,CAA K58Q XP_016885329.1

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