Product Details

SNP ID

rs28364766

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:29067959 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTCTGCTGCTGGACGCAGTGCCC[A/G]GGGCAGAAGTGAGCCTTCTCACCCT

Phenotype

MIM: 607350

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HMBOX1 PubMed Links

Additional Information

For this assay, SNP(s) [rs76644623] 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

HMBOX1

Gene Name

homeobox containing 1

There are no transcripts associated with this gene.

Gene

KIF13B

Gene Name

kinesin family member 13B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015254.3	8133	UTR 3			NP_056069.2
XM_005273458.1	8133	UTR 3			XP_005273515.1
XM_011544457.1	8133	UTR 3			XP_011542759.1
XM_011544458.1	8133	UTR 3			XP_011542760.1
XM_011544459.2	8133	UTR 3			XP_011542761.1
XM_011544460.2	8133	UTR 3			XP_011542762.1
XM_011544461.1	8133	UTR 3			XP_011542763.1
XM_017013257.1	8133	Intron			XP_016868746.1

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