Product Details

SNP ID

rs111438636

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:42736197 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGTGAATGCTCTTCCTTTCTCCCT[A/C]CCCCCCAGCCCAGAATATCAACACC

Phenotype

MIM: 610036

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CLDN19 PubMed Links

Gene Details

Gene

CLDN19

Gene Name

claudin 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001123395.1		Intron			NP_001116867.1
NM_001185117.1		Intron			NP_001172046.1
NM_148960.2		Intron			NP_683763.2

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