Product Details

SNP ID

rs76855155

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:42733759 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTGTGCCCCGGTGGATGTGCAGC[A/G]CCGGCCAGGCCAGGCGCCGAGGGGT

Phenotype

MIM: 610036

Polymorphism

A/G, Transition 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	2193	UTR 3			NP_001116867.1
NM_001185117.1	2193	UTR 3			NP_001172046.1
NM_148960.2	2193	UTR 3			NP_683763.2

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