Product Details

SNP ID

rs116854597

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:26639170 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGGGTCCTGTGGATGGGCCCTAA[A/C]CCAATCTGACTGGTGTCCTTTTAAG

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

C7orf71 PubMed Links

Additional Information

For this assay, SNP(s) [rs57000259] 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

C7orf71

Gene Name

chromosome 7 open reading frame 71

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145531.2	3232	Missense Mutation	AAC,ACC	N9T	NP_001139003.1
NM_001302625.1	3232	UTR 5			NP_001289554.1
XM_017012010.1	3232	Missense Mutation	AAC,ACC	N9T	XP_016867499.1
XM_017012011.1	3232	Missense Mutation	AAC,ACC	N9T	XP_016867500.1
XM_017012012.1	3232	Intron			XP_016867501.1
XM_017012013.1	3232	Intron			XP_016867502.1
XM_017012014.1	3232	Intron			XP_016867503.1

View Full Product Details