Product Details

SNP ID
rs201821077
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:69509202 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTGGAGAGATGCATGTTCGACCA[A/G]TGCTCTCTCAGCCAGCCTACTCTTT
Phenotype
MIM: 602876
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
OCLN PubMed Links

Gene Details

Gene
OCLN
Gene Name
occludin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001205254.1 548 Missense Mutation ATG,GTG M38V NP_001192183.1
NM_001205255.1 548 Intron NP_001192184.1
NM_002538.3 548 Missense Mutation ATG,GTG M38V NP_002529.1
XM_017008913.1 548 Missense Mutation ATG,GTG M38V XP_016864402.1
XM_017008914.1 548 Missense Mutation ATG,GTG M38V XP_016864403.1

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