Product Details

SNP ID

rs912075

Assay Type

Validated

NCBI dbSNP Submissions

57

Location

Chr.1:42734855 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TAGGACCTCTGAATTATTTCTTGCT[C/T]AGCCCTGGATGTGCTATGTAACCCA

Phenotype

MIM: 610036

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CLDN19 PubMed Links

Gene Details

Gene

CLDN19

Gene Name

claudin 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001123395.1	1097	UTR 3			NP_001116867.1
NM_001185117.1	1097	UTR 3			NP_001172046.1
NM_148960.2	1097	UTR 3			NP_683763.2

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