Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605360 MIM: 602364 MIM: 608296 MIM: 136515 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC85B 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 | 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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CCDC85B - coiled-coil domain containing 85B | ||||||
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There are no transcripts associated with this gene. |
CTSW - cathepsin W | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001335.3 | 1172 | Intron | NP_001326.2 |
FIBP - FGF1 intracellular binding protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004214.4 | 1172 | Missense Mutation | ATG,GTG | M,V 344 | NP_004205.2 | |
NM_198897.1 | 1172 | Missense Mutation | ATG,GTG | M,V 351 | NP_942600.1 |
FOSL1 - FOS like 1, AP-1 transcription factor subunit | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |