Product Details

SNP ID

rs4462

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:35301399 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCCCTGGAAATCGCTTGGCAGTAG[A/G]TCTCATAGGTGCTCATTCTTGGGCA

Phenotype

MIM: 604702 MIM: 604700

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HMGXB4 PubMed Links

Additional Information

For this assay, SNP(s) [rs80067987] are located under a primer 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

HMGXB4

Gene Name

HMG-box containing 4

There are no transcripts associated with this gene.

Gene

TOM1

Gene Name

target of myb1 membrane trafficking protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135729.1		Intron			NP_001129201.1
NM_001135730.1		Intron			NP_001129202.1
NM_001135732.1		Intron			NP_001129204.1
NM_005488.2		Intron			NP_005479.1
XM_011529818.2		Intron			XP_011528120.1
XM_011529820.2		Intron			XP_011528122.1
XM_017028529.1		Intron			XP_016884018.1
XM_017028530.1		Intron			XP_016884019.1

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