Product Details

SNP ID
rs138389932
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:98517054 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAAGTATGATGACAAAACCTACCT[C/G]CAAGGAGATGGAGAATGCCCGTGGC
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CLDND1 PubMed Links

Gene Details

Gene
CLDND1
Gene Name
claudin domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040181.1 465 Missense Mutation GCA,GGA A180G NP_001035271.1
NM_001040182.1 465 Missense Mutation GCA,GGA A203G NP_001035272.1
NM_001040183.1 465 Missense Mutation GCA,GGA A180G NP_001035273.1
NM_001040199.1 465 Missense Mutation GCA,GGA A180G NP_001035289.1
NM_001040200.1 465 Missense Mutation GCA,GGA A85G NP_001035290.1
NM_019895.2 465 Missense Mutation GCA,GGA A180G NP_063948.1

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