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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 180465 MIM: 602671 MIM: 610971 | ||||||||||||||||||||
Literature Links: |
CCDC84 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 |
CCDC84 - coiled-coil domain containing 84 | ||||||
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There are no transcripts associated with this gene. |
MIR3656 - microRNA 3656 | ||||||
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There are no transcripts associated with this gene. |
RPS25 - ribosomal protein S25 | ||||||
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There are no transcripts associated with this gene. |
SLC37A4 - solute carrier family 37 member 4 | ||||||
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There are no transcripts associated with this gene. |
TRAPPC4 - trafficking protein particle complex 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318486.1 | 728 | Intron | NP_001305415.1 | |||
NM_001318488.1 | 728 | Missense Mutation | ACT,ATT | T,I 134 | NP_001305417.1 | |
NM_001318489.1 | 728 | Intron | NP_001305418.1 | |||
NM_001318490.1 | 728 | Missense Mutation | ACT,ATT | T,I 91 | NP_001305419.1 | |
NM_001318492.1 | 728 | Missense Mutation | ACT,ATT | T,I 29 | NP_001305421.1 | |
NM_001318494.1 | 728 | Intron | NP_001305423.1 | |||
NM_016146.5 | 728 | Missense Mutation | ACT,ATT | T,I 134 | NP_057230.1 |