Product Details

SNP ID

rs201459139

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:71626482 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGGAGAGAGAGAGGGAAAGAGAC[A/C]CGGACCGAGGCCCCCGCCGGGACAC

Phenotype

MIM: 614094

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

MARVELD3 PubMed Links

Additional Information

For this assay, SNP(s) [rs4788821] 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

MARVELD3

Gene Name

MARVEL domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017967.3	330	Missense Mutation	ACG,CCG	T85P	NP_001017967.2
NM_001271329.1	330	Missense Mutation	ACG,CCG	T85P	NP_001258258.1
NM_052858.5	330	Missense Mutation	ACG,CCG	T85P	NP_443090.4
XM_011523449.2	330	Missense Mutation	ACG,CCG	T85P	XP_011521751.1

View Full Product Details