Product Details

SNP ID

rs28562785

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:69509542 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCCATGGCTGCCTTTTGTTTCATTG[C/T]CGCGTTGGTGATCTTTGTTACCAGT

Phenotype

MIM: 602876

Polymorphism

C/T, 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	888	Missense Mutation	GCC,GTC	A151V	NP_001192183.1
NM_001205255.1	888	Intron			NP_001192184.1
NM_002538.3	888	Missense Mutation	GCC,GTC	A151V	NP_002529.1
XM_017008913.1	888	Missense Mutation	GCC,GTC	A151V	XP_016864402.1
XM_017008914.1	888	Missense Mutation	GCC,GTC	A151V	XP_016864403.1

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