Product Details

SNP ID

rs9471614

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:41642309 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCACCTTCTGCAGTACATGAATTG[C/T]ACATCCACACGGGGGGCCTCCTTCA

Phenotype

MIM: 604971

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MDFI PubMed Links

Additional Information

For this assay, SNP(s) [rs77094739] 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

MDFI

Gene Name

MyoD family inhibitor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300804.1		Intron			NP_001287733.1
NM_001300805.1		Intron			NP_001287734.1
NM_001300806.1		Intron			NP_001287735.1
NM_005586.3		Intron			NP_005577.1
XM_005249117.3		Intron			XP_005249174.1
XM_011514625.2		Intron			XP_011512927.1
XM_011514626.2		Intron			XP_011512928.1
XM_017010867.1		Intron			XP_016866356.1

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