Product Details

SNP ID

rs4279261

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:185457636 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTCTTGACAGTATAAAATATATAC[C/T]TAATTCCAATTTCTAATTTTAAAAA

Phenotype

MIM: 609488

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C4orf47 PubMed Links

Additional Information

For this assay, SNP(s) [rs73873459] 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

C4orf47

Gene Name

chromosome 4 open reading frame 47

There are no transcripts associated with this gene.

Gene

CCDC110

Gene Name

coiled-coil domain containing 110

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145411.1		Intron			NP_001138883.1
NM_152775.3		Intron			NP_689988.1
XM_005262891.3		Intron			XP_005262948.1
XM_006714172.2		Intron			XP_006714235.1
XM_011531827.2		Intron			XP_011530129.1
XM_011531828.2		Intron			XP_011530130.1
XM_011531829.2		Intron			XP_011530131.1
XM_017007987.1		Intron			XP_016863476.1
XM_017007988.1		Intron			XP_016863477.1

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