Product Details

SNP ID

rs7624719

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:197755816 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGGGTCATCTTTAAAAAATGGAG[C/G]CTTCTGTGATTATGGGAAGTAAGTA

Phenotype

MIM: 616933 MIM: 613516

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FYTTD1 PubMed Links

Additional Information

For this assay, SNP(s) [rs148567326] 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

FYTTD1

Gene Name

forty-two-three domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001011537.2	245	Missense Mutation	CCT,GCT	P3A	NP_001011537.2
NM_032288.6	245	Intron			NP_115664.2

Gene

RUBCN

Gene Name

RUN and cysteine rich domain containing beclin 1 interacting protein

There are no transcripts associated with this gene.

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