Product Details

SNP ID

rs139388349

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:137999020 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTTCAACTACCAGGGGCTGTGGC[A/G]CTCCTGTGTCCGAGAGAGCTCTGGC

Phenotype

MIM: 609210

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLDN18 PubMed Links

Gene Details

Gene

CLDN18

Gene Name

claudin 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002026.2	205	Missense Mutation	CAC,CGC	H51R	NP_001002026.1
NM_016369.3	205	Intron			NP_057453.1

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