Product Details

SNP ID

rs28513225

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:69492986 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGCGACTATGTTAGGGGAGGTGC[C/T]GGGGGGAGGACGCTCCGCGCTGGTT

Phenotype

MIM: 602876

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC101928924 PubMed Links

Additional Information

For this assay, SNP(s) [rs114120250] 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

LOC101928924

Gene Name

uncharacterized LOC101928924

There are no transcripts associated with this gene.

Gene

OCLN

Gene Name

occludin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001205254.1		Intron			NP_001192183.1
NM_001205255.1		Intron			NP_001192184.1
NM_002538.3		Intron			NP_002529.1
XM_017008913.1		Intron			XP_016864402.1
XM_017008914.1		Intron			XP_016864403.1

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