Product Details

SNP ID

rs6965212

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:139341719 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACTCGGGGACCAAAGGACCAGCGG[G/T]GGGGGGCGCAGAGTCGCTCTGGGGA

Phenotype

MIM: 613056

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

C7orf55-LUC7L2 PubMed Links

Additional Information

For this assay, SNP(s) [rs116523410] 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

C7orf55-LUC7L2

Gene Name

C7orf55-LUC7L2 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001244584.2		Intron			NP_001231513.1

Gene

FMC1

Gene Name

formation of mitochondrial complex V assembly factor 1 homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_197964.4		Intron			NP_932068.2

Gene

LUC7L2

Gene Name

LUC7 like 2, pre-mRNA splicing factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001244585.1		Intron			NP_001231514.1
NM_001270643.1		Intron			NP_001257572.1
NM_016019.4		Intron			NP_057103.2

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