Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCCCTGGACAAACTCGGGCGTGGC[A/G]CACGTGGGCTGCTGCCGGTTGAAGT
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) - 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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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 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288115.1 | |
NM_001301187.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288116.1 | |
NM_001301189.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288118.1 | |
NM_001301191.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288120.1 | |
NM_001301192.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288121.1 | |
NM_001301194.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288123.1 | |
NM_001301195.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288124.1 | |
NM_001301197.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288126.1 | |
NM_001301198.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288127.1 | |
NM_001301199.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288128.1 | |
NM_001301200.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | NP_001288129.1 | |
NM_032808.6 | 1382 | Silent Mutation | TGC,TGT | C,C 396 | NP_116197.4 | |
XM_011522118.2 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | XP_011520420.1 | |
XM_017022682.1 | 1382 | Silent Mutation | TGC,TGT | C,C 390 | XP_016878171.1 |