Product Details

SNP ID

rs137943992

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:30462571 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTTCCTTCAGCTTCGCAGCCTT[C/T]TTTTCATAAGGCTGCTTGTCATCTG

Phenotype

MIM: 163905

Polymorphism

C/T, 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	1379	Silent Mutation			NP_001300821.1
NM_001313893.1	1379	Silent Mutation			NP_001300822.1
NM_002128.5	1379	Silent Mutation			NP_002119.1

View Full Product Details