Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
47 submissions
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Phenotype: |
MIM: 611354 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACAP3 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ACAP3 - ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 | ||||||
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There are no transcripts associated with this gene. |
CPSF3L - cleavage and polyadenylation specific factor 3-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256456.1 | 1875 | Silent Mutation | CCA,CCG | P,P 553 | NP_001243385.1 | |
NM_001256460.1 | 1875 | Silent Mutation | CCA,CCG | P,P 518 | NP_001243389.1 | |
NM_001256462.1 | 1875 | Silent Mutation | CCA,CCG | P,P 449 | NP_001243391.1 | |
NM_001256463.1 | 1875 | Silent Mutation | CCA,CCG | P,P 446 | NP_001243392.1 | |
NM_017871.5 | 1875 | Silent Mutation | CCA,CCG | P,P 547 | NP_060341.2 | |
XM_011541647.1 | 1875 | Silent Mutation | CCA,CCG | P,P 607 | XP_011539949.1 | |
XM_011541648.1 | 1875 | Silent Mutation | CCA,CCG | P,P 569 | XP_011539950.1 | |
XM_011541650.1 | 1875 | Silent Mutation | CCA,CCG | P,P 423 | XP_011539952.1 | |
XM_017001557.1 | 1875 | Silent Mutation | CCA,CCG | P,P 423 | XP_016857046.1 | |
XM_017001558.1 | 1875 | Silent Mutation | CCA,CCG | P,P 423 | XP_016857047.1 |
MIR6727 - microRNA 6727 | ||||||
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There are no transcripts associated with this gene. |
PUSL1 - pseudouridylate synthase-like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153339.1 | 1875 | Intron | NP_699170.1 | |||
XM_005244720.3 | 1875 | Intron | XP_005244777.1 |
Set Membership: |
Validated |