Product Details

SNP ID

rs141774128

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51347012 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGCCCCCATCGATCTCCCGCTCC[A/G]CTTTCAACTTGTCCCCCTCCAGCGT

Phenotype

MIM: 130410

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ETFB PubMed Links

Additional Information

For this assay, SNP(s) [rs144640661] 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

ETFB

Gene Name

electron transfer flavoprotein beta subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001014763.1	577	Missense Mutation	GCG,GTG	A253V	NP_001014763.1
NM_001985.2	577	Missense Mutation	GCG,GTG	A162V	NP_001976.1

Gene

VSIG10L

Gene Name

V-set and immunoglobulin domain containing 10 like

There are no transcripts associated with this gene.

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