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CCCCAGACCTCTGCCATACACTCAG[A/G]GATTTCTTTTGCCCTTTATTCCGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616312 MIM: 158270 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LEMD2 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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LEMD2 - LEM domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
MLN - motilin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040109.1 | 221 | Silent Mutation | TCC,TCT | S,S 50 | NP_001035198.1 | |
NM_001184698.1 | 221 | Silent Mutation | TCC,TCT | S,S 50 | NP_001171627.1 | |
NM_002418.2 | 221 | Silent Mutation | TCC,TCT | S,S 50 | NP_002409.1 |