Product Details

SNP ID
rs150638510
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:150987790 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTTCCTCTAGGATGTTGCTGACT[A/G]TAAGTCGAAAGGAAAGTTTGATGGT
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_001301228.1 586 Missense Mutation TAT,TGT Y160C NP_001288157.1
NM_001301229.1 586 Missense Mutation TAT,TGT Y160C NP_001288158.1
NM_001301231.1 586 Missense Mutation TAT,TGT Y180C NP_001288160.1
NM_005342.3 586 Missense Mutation TAT,TGT Y160C NP_005333.2

View Full Product Details