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GTGTGAAATCAGTGGAGTGGCAGGG[G/T]CCCAGCCAGTGAGTGAGAAGCAGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602129 MIM: 610675 | ||||||||||||||||||||
Literature Links: |
MYO9B 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 |
MYO9B - myosin IXB | ||||||
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There are no transcripts associated with this gene. |
OCEL1 - occludin/ELL domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
USE1 - unconventional SNARE in the ER 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018467.3 | 496 | Missense Mutation | GCC,TCC | A,S 146 | NP_060937.1 | |
XM_017026975.1 | 496 | Missense Mutation | GCC,TCC | A,S 146 | XP_016882464.1 | |
XM_017026976.1 | 496 | Missense Mutation | GCC,TCC | A,S 76 | XP_016882465.1 |