Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609791 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINGO1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LINGO1 - leucine rich repeat and Ig domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301186.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288115.1 | |
NM_001301187.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288116.1 | |
NM_001301189.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288118.1 | |
NM_001301191.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288120.1 | |
NM_001301192.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288121.1 | |
NM_001301194.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288123.1 | |
NM_001301195.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288124.1 | |
NM_001301197.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288126.1 | |
NM_001301198.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288127.1 | |
NM_001301199.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288128.1 | |
NM_001301200.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | NP_001288129.1 | |
NM_032808.6 | 1298 | Silent Mutation | TCC,TCT | S,S 368 | NP_116197.4 | |
XM_011522118.2 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | XP_011520420.1 | |
XM_017022682.1 | 1298 | Silent Mutation | TCC,TCT | S,S 362 | XP_016878171.1 |
Set Membership: |
HapMap |