Product Details

SNP ID

rs200915238

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:74588616 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCTTTTGAGATTCTCCATGGTCA[C/T]GGTGAACACGTGGTTTTTCTGATTG

Phenotype

MIM: 616301

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C17orf77 PubMed Links

Additional Information

For this assay, SNP(s) [rs783239] are located under a probe 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

C17orf77

Gene Name

chromosome 17 open reading frame 77

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302809.1	303	Intron			NP_001289738.1
NM_152460.2	303	Intron			NP_689673.2

Gene

CD300LD

Gene Name

CD300 molecule like family member d

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001115152.1	303	Missense Mutation	ATG,GTG	M92V	NP_001108624.1

Gene

LOC101928343

Gene Name

uncharacterized LOC101928343

There are no transcripts associated with this gene.

View Full Product Details