Product Details

SNP ID

rs201399564

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:42735965 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCGGGCATGTGCAGCAGAGGAAG[C/G]AGCCGCCCAGCACGGCCAGGCCAGC

Phenotype

MIM: 610036

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CLDN19 PubMed Links

Additional Information

For this assay, SNP(s) [rs4660658] 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

CLDN19

Gene Name

claudin 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001123395.1	730	Missense Mutation	TCC,TGC	S180C	NP_001116867.1
NM_001185117.1	730	Missense Mutation	CCT,GCT	P152A	NP_001172046.1
NM_148960.2	730	Missense Mutation	TCC,TGC	S180C	NP_683763.2

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