Product Details

SNP ID

rs28526523

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:138005853 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGCTGACAAAGAGTTATATGTAA[G/T]ATGTTCATCATAACATTGCCTTTTA

Phenotype

MIM: 609210

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CLDN18 PubMed Links

Additional Information

For this assay, SNP(s) [rs199961457] 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

CLDN18

Gene Name

claudin 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002026.2		Intron			NP_001002026.1
NM_016369.3		Intron			NP_057453.1

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