Product Details

SNP ID

rs190963991

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:8702458 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTGGCGCCCTGCGGGCTCCTGCT[C/G]AACCTGACCGGCACCCTGGCGCCCG

Phenotype

MIM: 609203

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CLDN23 PubMed Links

Gene Details

Gene

CLDN23

Gene Name

claudin 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_194284.2	303	Silent Mutation	CTC,CTG	L20L	NP_919260.2

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