Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 159465 | ||||||||||||||||||||
Literature Links: |
MOG 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 |
MOG - myelin oligodendrocyte glycoprotein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008228.2 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_001008229.1 | |
NM_001008229.2 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_001008230.1 | |
NM_001170418.1 | 400 | Intron | NP_001163889.1 | |||
NM_002433.4 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_002424.3 | |
NM_206809.3 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_996532.2 | |
NM_206810.3 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_996533.2 | |
NM_206811.3 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_996534.2 | |
NM_206812.3 | 400 | Silent Mutation | CCC,CCT | P,P 57 | NP_996535.2 | |
NM_206814.5 | 400 | Intron | NP_996537.3 | |||
XM_005249131.3 | 400 | Silent Mutation | CCC,CCT | P,P 57 | XP_005249188.1 |