Product Details

SNP ID

rs2131738

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:57603970 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTTGCCTATACTTGTGAAATGAG[A/C]TCATTCTATACATATTCTTATGGAA

Phenotype

MIM: 614071

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

GCOM1 PubMed Links

Additional Information

For this assay, SNP(s) [rs116406769] 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

GCOM1

Gene Name

GRINL1A complex locus 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018090.6		Intron			NP_001018100.1
NM_001018091.6		Intron			NP_001018101.1
NM_001285900.3		Intron			NP_001272829.1

Gene

MYZAP

Gene Name

myocardial zonula adherens protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018100.4		Intron			NP_001018110.1
NM_152451.7		Intron			NP_689664.3

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