Product Details

SNP ID

rs116804195

Assay Type

Functionally Tested

NCBI dbSNP Submissions

29

Location

Chr.1:42735905 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGGGCAGCAGCAGAGGGTCCAGGC[C/T]GATAGGGCTGTGGGCTGCTGTTGGG

Phenotype

MIM: 610036

Polymorphism

C/T, Transition 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	790	Missense Mutation	CAG,CGG	Q200R	NP_001116867.1
NM_001185117.1	790	Missense Mutation	AGC,GGC	S172G	NP_001172046.1
NM_148960.2	790	Missense Mutation	CAG,CGG	Q200R	NP_683763.2

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