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CAACTGCTCAGTCTTCTGGATCTCT[A/G]TATGGTTCACAAATATATGCCCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602876 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OCLN 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) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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OCLN - occludin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001205254.1 | 1057 | Silent Mutation | CTA,CTG | L,L 207 | NP_001192183.1 | |
NM_001205255.1 | 1057 | Intron | NP_001192184.1 | |||
NM_002538.3 | 1057 | Silent Mutation | CTA,CTG | L,L 207 | NP_002529.1 | |
XM_017008913.1 | 1057 | Silent Mutation | CTA,CTG | L,L 207 | XP_016864402.1 | |
XM_017008914.1 | 1057 | Silent Mutation | CTA,CTG | L,L 207 | XP_016864403.1 |