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AGCCTCCAAGGAAGCCATTAGCATG[C/T]CGGTAACCGAGTGTGTGGTTGATAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609211 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC104968399 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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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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LOC104968399 - uncharacterized LOC104968399 | ||||||
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There are no transcripts associated with this gene. |
MYL12A - myosin light chain 12A | ||||||
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There are no transcripts associated with this gene. |
MYL12B - myosin light chain 12B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144944.1 | Intron | NP_001138416.1 | ||||
NM_001144945.1 | Intron | NP_001138417.1 | ||||
NM_033546.3 | Intron | NP_291024.1 |
Set Membership: |
Validated |