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

View Full Product Details