Product Details

SNP ID
rs141917987
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:150986092 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAATCTAAATTTGATGAAATGGC[A/G]AAGGCAGATAAAGTGCGCTATGATC
Phenotype
MIM: 300193
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HMGB3 PubMed Links

Gene Details

Gene
HMGB3
Gene Name
high mobility group box 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301228.1 299 Silent Mutation GCA,GCG A64A NP_001288157.1
NM_001301229.1 299 Silent Mutation GCA,GCG A64A NP_001288158.1
NM_001301231.1 299 Silent Mutation GCA,GCG A84A NP_001288160.1
NM_005342.3 299 Silent Mutation GCA,GCG A64A NP_005333.2

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