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TTTCTTCATGGCCTTGTCAATGAGC[C/T]GCTCCAGTTCCTTGGCCTGGTTGTT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615778 MIM: 609003 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLDN15 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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CLDN15 - claudin 15 | ||||||
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There are no transcripts associated with this gene. |
FIS1 - fission, mitochondrial 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016068.2 | 421 | Missense Mutation | CAG,CGG | Q,R 112 | NP_057152.2 |