Product Details

SNP ID

rs11638276

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.15:89737814 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AAACAGAGAGAGCCCCTCCGATCTC[C/G]TCCCCACTCTGTGTCCCCCTCTACC

Phenotype

MIM: 608689

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

MESP1 PubMed Links

Additional Information

For this assay, SNP(s) [rs75167608,rs75510286] 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

MESP1

Gene Name

mesoderm posterior bHLH transcription factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018670.3		Intron			NP_061140.1

Gene

WDR93

Gene Name

WD repeat domain 93

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284395.1		Intron			NP_001271324.1
NM_001284396.1		Intron			NP_001271325.1
NM_020212.1		Intron			NP_064597.1
XM_006720614.1		Intron			XP_006720677.1
XM_006720615.1		Intron			XP_006720678.1
XM_006720618.2		Intron			XP_006720681.1
XM_011521794.2		Intron			XP_011520096.1
XM_011521795.1		Intron			XP_011520097.1
XM_011521796.2		Intron			XP_011520098.1
XM_011521798.2		Intron			XP_011520100.1
XM_011521800.1		Intron			XP_011520102.1
XM_011521802.2		Intron			XP_011520104.1
XM_017022415.1		Intron			XP_016877904.1
XM_017022416.1		Intron			XP_016877905.1
XM_017022417.1		Intron			XP_016877906.1

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