Product Details

SNP ID

rs146427219

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:30166066 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTCTTTCTGTTGCAGCAGCAAAA[C/T]CCACAAAGCAGACCCCCTCCAATGA

Phenotype

MIM: 617005

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CLDN17 PubMed Links

Gene Details

Gene

CLDN17

Gene Name

claudin 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012131.2	588	Silent Mutation	GGA,GGG	G184G	NP_036263.1

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