Product Details

SNP ID

rs61743574

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:114922368 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGAGGCAGAGAGGGGGAAGGCCC[C/T]CTCGCAGGGGAGCCGGCTGGAGTGA

Phenotype

MIM: 614511

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MDFIC PubMed Links

Additional Information

For this assay, SNP(s) [rs75938219] 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

MDFIC

Gene Name

MyoD family inhibitor domain containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166345.1	215	UTR 5			NP_001159817.1
NM_001166346.1	215	UTR 5			NP_001159818.3
NM_199072.4	215	UTR 5			NP_951038.1

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