Product Details

SNP ID
rs146755542
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:36461272 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGTTGTAGAAGTTCTGCACCACGT[C/T]GTTGGTGGTCCAGGAGACGGCCACC
Phenotype
MIM: 605608
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CLDN14 PubMed Links

Gene Details

Gene
CLDN14
Gene Name
claudin 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146077.1 898 Missense Mutation AAC,GAC N142D NP_001139549.1
NM_001146078.2 898 Missense Mutation AAC,GAC N142D NP_001139550.1
NM_001146079.1 898 Missense Mutation AAC,GAC N142D NP_001139551.1
NM_012130.3 898 Missense Mutation AAC,GAC N142D NP_036262.1
NM_144492.2 898 Missense Mutation AAC,GAC N142D NP_652763.1

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