Product Details

SNP ID
rs150842119
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:35263108 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGATGGTGATCATACCTTTGAGG[A/G]CATAGGACTTGCAGCTGGCCGAAGC
Phenotype
MIM: 604702
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
HMGXB4 PubMed Links

Gene Details

Gene
HMGXB4
Gene Name
HMG-box containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001003681.2 236 Missense Mutation GAC,GGC D21G NP_001003681.1
XM_006724100.3 236 Missense Mutation GAC,GGC D64G XP_006724163.1
XM_006724101.3 236 Missense Mutation GAC,GGC D64G XP_006724164.1
XM_006724102.1 236 UTR 5 XP_006724165.1

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