Product Details

SNP ID

rs2371088

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:39811590 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCTGCGTCTCTCCTAATTACCCAC[C/T]ACTACCTCCATCTGCGAGCTGTCTC

Phenotype

MIM: 611790

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYRIP PubMed Links

Additional Information

For this assay, SNP(s) [rs77825791] 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

MYRIP

Gene Name

myosin VIIA and Rab interacting protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284423.1		Intron			NP_001271352.1
NM_001284424.1		Intron			NP_001271353.1
NM_001284425.1		Intron			NP_001271354.1
NM_001284426.1		Intron			NP_001271355.1
NM_015460.3		Intron			NP_056275.2
XM_011533575.1		Intron			XP_011531877.1

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