Product Details

SNP ID

rs112851119

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:35263211 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCTGCTCAGGTCAGGAATTCTTC[A/C]AAGAAGAAGTTGAAGGTAAGTCCTG

Phenotype

MIM: 604702

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

HMGXB4 PubMed Links

Gene Details

Gene

HMGXB4

Gene Name

HMG-box containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003681.2	339	Silent Mutation	TCA,TCC	S55S	NP_001003681.1
XM_006724100.3	339	Silent Mutation	TCA,TCC	S98S	XP_006724163.1
XM_006724101.3	339	Silent Mutation	TCA,TCC	S98S	XP_006724164.1
XM_006724102.1	339	UTR 5			XP_006724165.1

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