Search Thermo Fisher Scientific
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GCAGCCCAGATGAAGAGAGCAGAAG[A/C]CATGAACTGTAAGGGAGCAGAGACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CLDND1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CLDND1 - claudin domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040181.1 | 611 | Missense Mutation | GCT,TCT | A,S 229 | NP_001035271.1 | |
NM_001040182.1 | 611 | Missense Mutation | GCT,TCT | A,S 252 | NP_001035272.1 | |
NM_001040183.1 | 611 | Missense Mutation | GCT,TCT | A,S 229 | NP_001035273.1 | |
NM_001040199.1 | 611 | Missense Mutation | GCT,TCT | A,S 229 | NP_001035289.1 | |
NM_001040200.1 | 611 | Missense Mutation | GCT,TCT | A,S 134 | NP_001035290.1 | |
NM_019895.2 | 611 | Missense Mutation | GCT,TCT | A,S 229 | NP_063948.1 |