Product Details

SNP ID

rs12505562

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:5539923 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACTTCTGCTCTTCAAAAGATACCG[C/T]TGAAAGAATGAAAAGACAAACTGCA

Phenotype

MIM: 607261

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EVC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs141510342] 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

EVC2

Gene Name

EvC ciliary complex subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166136.1		Intron			NP_001159608.1
NM_147127.4		Intron			NP_667338.3
XM_017007735.1		Intron			XP_016863224.1
XM_017007736.1		Intron			XP_016863225.1
XM_017007737.1		Intron			XP_016863226.1
XM_017007738.1		Intron			XP_016863227.1
XM_017007739.1		Intron			XP_016863228.1

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