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GGCAGAAGGACCATCCAAATTCACC[A/G]GATACATTGTCAGGGAGCTCTAGTT
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 | |||
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Global
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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 | 553 | Silent Mutation | TCC,TCT | S,S 209 | NP_001035271.1 | |
NM_001040182.1 | 553 | Silent Mutation | TCC,TCT | S,S 232 | NP_001035272.1 | |
NM_001040183.1 | 553 | Silent Mutation | TCC,TCT | S,S 209 | NP_001035273.1 | |
NM_001040199.1 | 553 | Silent Mutation | TCC,TCT | S,S 209 | NP_001035289.1 | |
NM_001040200.1 | 553 | Silent Mutation | TCC,TCT | S,S 114 | NP_001035290.1 | |
NM_019895.2 | 553 | Silent Mutation | TCC,TCT | S,S 209 | NP_063948.1 |