Product Details

SNP ID

rs59255697

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:44519915 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATAAACAGGAAAAAAAAAAAAAAC[C/T]TTCCTATTGTCCAGGTAGAGCACAT

Phenotype

MIM: 602320

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NELL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs34690332] 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

NELL2

Gene Name

neural EGFL like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145107.1		Intron			NP_001138579.1
NM_001145108.1		Intron			NP_001138580.1
NM_001145109.1		Intron			NP_001138581.1
NM_001145110.1		Intron			NP_001138582.1
NM_006159.2		Intron			NP_006150.1
XM_005268905.3		Intron			XP_005268962.1
XM_011538396.1		Intron			XP_011536698.1
XM_017019341.1		Intron			XP_016874830.1
XM_017019342.1		Intron			XP_016874831.1
XM_017019343.1		Intron			XP_016874832.1
XM_017019344.1		Intron			XP_016874833.1

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