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GCTACACAGGCTCCGAAGCTTCCCC[C/T]TGGGTGGCAGCTGGATATGGGTTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
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Phenotype: |
MIM: 609794 MIM: 602943 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINGO4 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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LINGO4 - leucine rich repeat and Ig domain containing 4 | ||||||
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There are no transcripts associated with this gene. |
RORC - RAR related orphan receptor C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001523.1 | 2297 | Missense Mutation | AAG,AGG | K,R 448 | NP_001001523.1 | |
NM_005060.3 | 2297 | Missense Mutation | AAG,AGG | K,R 469 | NP_005051.2 | |
XM_006711484.3 | 2297 | Missense Mutation | AAG,AGG | K,R 602 | XP_006711547.2 |