Product Details
- SNP ID
-
rs202151198
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:8702511 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGGCGGCTGGTGAAGGGCTTCCTGA[A/C]CCAGCCAGTGGACGTGGAGTTGTAC
- Phenotype
-
MIM: 609203
- Polymorphism
- A/C, 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 |
356 |
Missense Mutation |
AAC,ACC |
N38T |
NP_919260.2 |
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