Product Details

SNP ID

rs751828

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:30617837 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGACCGGAAGTGCTCACGTCTTCAC[A/C]TTCCCCGCCACGCCACCGTCCTTTC

Phenotype

MIM: 163905

Polymorphism

A/C, Transversion 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	441	Intron			NP_001300821.1
NM_001313893.1	441	Intron			NP_001300822.1
NM_002128.5	441	Intron			NP_002119.1

Gene

USPL1

Gene Name

ubiquitin specific peptidase like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321532.1	441	UTR 5			NP_001308461.1
NM_001321533.1	441	UTR 5			NP_001308462.1
NM_001321534.1	441	Intron			NP_001308463.1
NM_005800.4	441	UTR 5			NP_005791.3
XM_005266213.3	441	UTR 5			XP_005266270.1
XM_006719751.3	441	UTR 5			XP_006719814.1
XM_017020314.1	441	UTR 5			XP_016875803.1
XM_017020315.1	441	Intron			XP_016875804.1
XM_017020316.1	441	UTR 5			XP_016875805.1

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