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GGCTGCTGCCAAAGGCCTTCTCCTC[A/G]TTGTCACTGCAGAGGCACAGGGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 308840 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
L1CAM 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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L1CAM - L1 cell adhesion molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000425.4 | 3767 | Silent Mutation | AAC,AAT | N,N 1183 | NP_000416.1 | |
NM_001143963.2 | 3767 | Silent Mutation | AAC,AAT | N,N 1174 | NP_001137435.1 | |
NM_001278116.1 | 3767 | Silent Mutation | AAC,AAT | N,N 1183 | NP_001265045.1 | |
NM_024003.3 | 3767 | Silent Mutation | AAC,AAT | N,N 1179 | NP_076493.1 |