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TTTTCACATTCTTTAATTTTTGTTT[A/G]CCCTTTTCCGGGTTGAAGGTTCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604875 MIM: 604485 | ||||||||||||||||||||
Literature Links: |
MYO9A 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 |
MYO9A - myosin IXA | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006901.3 | 7941 | Silent Mutation | NP_008832.2 | |||
XM_006720539.2 | 7941 | Silent Mutation | XP_006720602.1 | |||
XM_011521613.2 | 7941 | Silent Mutation | XP_011519915.1 | |||
XM_011521614.2 | 7941 | Silent Mutation | XP_011519916.1 | |||
XM_011521615.2 | 7941 | Silent Mutation | XP_011519917.1 | |||
XM_011521616.2 | 7941 | Silent Mutation | XP_011519918.1 | |||
XM_011521617.2 | 7941 | Silent Mutation | XP_011519919.1 | |||
XM_011521618.2 | 7941 | Silent Mutation | XP_011519920.1 | |||
XM_011521619.2 | 7941 | Silent Mutation | XP_011519921.1 | |||
XM_011521620.2 | 7941 | Silent Mutation | XP_011519922.1 | |||
XM_011521621.2 | 7941 | Silent Mutation | XP_011519923.1 | |||
XM_011521622.2 | 7941 | Silent Mutation | XP_011519924.1 | |||
XM_011521623.2 | 7941 | Silent Mutation | XP_011519925.1 | |||
XM_017022228.1 | 7941 | Silent Mutation | XP_016877717.1 | |||
XM_017022229.1 | 7941 | Silent Mutation | XP_016877718.1 | |||
XM_017022230.1 | 7941 | Silent Mutation | XP_016877719.1 |
NR2E3 - nuclear receptor subfamily 2 group E member 3 | ||||||
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There are no transcripts associated with this gene. |