Product Details

SNP ID
rs2388544
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:30463210 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAAAAACAGGCAAGATACTCACGGA[A/G]GCCTCTTGGGTGCATTGGGATCCTT
Phenotype
MIM: 163905
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HMGB1 PubMed Links

Gene Details

Gene
HMGB1
Gene Name
high mobility group box 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001313892.1 1234 Missense Mutation CCT,CTT P98L NP_001300821.1
NM_001313893.1 1234 Missense Mutation CCT,CTT P98L NP_001300822.1
NM_002128.5 1234 Missense Mutation CCT,CTT P98L NP_002119.1

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