Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGCTCATTATTGTGATGTGCATTG[C/T]CATCTTTGCCTGTGTGGCCTCCACG
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 |
---|---|---|
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 |
OCLN - occludin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001205254.1 | 669 | Missense Mutation | GCC,GTC | A,V 78 | NP_001192183.1 | |
NM_001205255.1 | 669 | Intron | NP_001192184.1 | |||
NM_002538.3 | 669 | Missense Mutation | GCC,GTC | A,V 78 | NP_002529.1 | |
XM_017008913.1 | 669 | Missense Mutation | GCC,GTC | A,V 78 | XP_016864402.1 | |
XM_017008914.1 | 669 | Missense Mutation | GCC,GTC | A,V 78 | XP_016864403.1 |