Product Details

SNP ID

rs61733675

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:30462701 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGCGATACTCAGAGCAGAAGAGG[A/C]AGAAGGCCGAACTAAAAAAAAAATT

Phenotype

MIM: 163905

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

HMGB1 PubMed Links

Additional Information

For this assay, SNP(s) [rs1060348] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	1249	Missense Mutation	TGC,TTC	C103F	NP_001300821.1
NM_001313893.1	1249	Missense Mutation	TGC,TTC	C103F	NP_001300822.1
NM_002128.5	1249	Missense Mutation	TGC,TTC	C103F	NP_002119.1

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