Product Details

SNP ID

rs3926888

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36763306 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAAGGGCTGCAAACGCCTGAAGGC[A/G]AGGGCCAAATTTATGTGAGCCTTTG

Phenotype

MIM: 615870

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

IFT27 PubMed Links

Additional Information

For this assay, SNP(s) [rs74494195] 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

IFT27

Gene Name

intraflagellar transport 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177701.2		Intron			NP_001171172.1
NM_006860.4		Intron			NP_006851.1
XM_006724106.2		Intron			XP_006724169.1
XM_017028540.1		Intron			XP_016884029.1

Gene

LOC105373021

Gene Name

uncharacterized LOC105373021

There are no transcripts associated with this gene.

View Full Product Details