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Search Thermo Fisher Scientific
TCTCTATGTCGCTCTTTTCCTCTAT[C/T]ATGTTGATTGGCGGTGCCAAGCAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610174 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
EFCAB9 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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EFCAB9 - EF-hand calcium binding domain 9 | ||||||
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There are no transcripts associated with this gene. |
UBTD2 - ubiquitin domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152277.2 | 513 | Missense Mutation | ATA,ATG | I,M 129 | NP_689490.2 | |
XM_017010022.1 | 513 | Missense Mutation | ATA,ATG | I,M 85 | XP_016865511.1 | |
XM_017010023.1 | 513 | Missense Mutation | ATA,ATG | I,M 85 | XP_016865512.1 |
Set Membership: |
HapMap |