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GGTTCATGGCATCGGCCGTCTCAGT[A/G]GCGTCCTCCAGCTCGCGCTGCAGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 160775 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR6819 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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MIR6819 - microRNA 6819 | ||||||
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There are no transcripts associated with this gene. |
MYH9 - myosin, heavy chain 9, non-muscle | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002473.5 | 5744 | Silent Mutation | GCC,GCT | A,A 1903 | NP_002464.1 | |
XM_011530197.2 | 5744 | Silent Mutation | GCC,GCT | A,A 1903 | XP_011528499.1 | |
XM_017028803.1 | 5744 | Silent Mutation | GCC,GCT | A,A 1903 | XP_016884292.1 | |
XM_017028804.1 | 5744 | Silent Mutation | GCC,GCT | A,A 1903 | XP_016884293.1 | |
XM_017028805.1 | 5744 | Silent Mutation | GCC,GCT | A,A 1903 | XP_016884294.1 | |
XM_017028806.1 | 5744 | Silent Mutation | GCC,GCT | A,A 1903 | XP_016884295.1 |