Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCTCCTTGTATTGAAGGTTGGAC[C/G]AGTTGGTCCTGGTGGTCAGACACAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602909 MIM: 612546 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLDN4 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CLDN4 - claudin 4 | ||||||
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There are no transcripts associated with this gene. |
WBSCR27 - Williams Beuren syndrome chromosome region 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152559.2 | 632 | Missense Mutation | TCG,TGG | S,W 171 | NP_689772.2 | |
XM_017011777.1 | 632 | Missense Mutation | TCG,TGG | S,W 197 | XP_016867266.1 | |
XM_017011778.1 | 632 | Missense Mutation | TCG,TGG | S,W 197 | XP_016867267.1 |
Set Membership: |
HapMap |