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CTCCCAAGAAGCCTGAGCCTAAGAA[A/G]GAGGCAGCCAAGCCAGCTCCAGCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 160770 | ||||||||||||||||||||
Literature Links: |
MYL4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MYL4 - myosin light chain 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002841.1 | 105 | Silent Mutation | AAA,AAG | K,K 10 | NP_001002841.1 | |
NM_002476.2 | 105 | Silent Mutation | AAA,AAG | K,K 10 | NP_002467.1 | |
XM_005257391.4 | 105 | Silent Mutation | AAA,AAG | K,K 10 | XP_005257448.1 | |
XM_011524839.2 | 105 | Silent Mutation | AAA,AAG | K,K 10 | XP_011523141.2 | |
XM_017024683.1 | 105 | Silent Mutation | AAA,AAG | K,K 10 | XP_016880172.1 | |
XM_017024684.1 | 105 | Silent Mutation | AAA,AAG | K,K 10 | XP_016880173.1 |