Product Details

SNP ID

rs201678067

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:138010352 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTACGACAACCCCGTCACCTCC[A/G]TGTTCCAGTACGAAGGGCTCTGGAG

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	189	Intron			NP_001002026.1
NM_016369.3	189	Missense Mutation	ATG,GTG	M43V	NP_057453.1

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