Product Details

SNP ID

rs12009536

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:150985966 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACCTACCCCCTTTTGCAAGTGGTT[C/T]TAGCAACTGCTAGTTTAATCACAAG

Phenotype

MIM: 300193

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HMGB3 PubMed Links

Gene Details

Gene

HMGB3

Gene Name

high mobility group box 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301228.1		Intron			NP_001288157.1
NM_001301229.1		Intron			NP_001288158.1
NM_001301231.1		Intron			NP_001288160.1
NM_005342.3		Intron			NP_005333.2

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