Product Details
- SNP ID
-
rs200567790
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:73769897 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCCGGTGCTCTGCACCACGCAGTT[C/T]ATCCACAGGCCCTCCCAGATGTTCT
- Phenotype
-
MIM: 602910
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CLDN3
PubMed Links
Gene Details
- Gene
- CLDN3
- Gene Name
- claudin 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001306.3 |
374 |
Missense Mutation |
ATA,ATG |
I51M |
NP_001297.1 |
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