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CATGCTGGTGGAAGGCGAGTGGACA[C/T]TCCCAGCTGTGGGGTGGGGAGAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613541 MIM: 602198 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C12orf65 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 | 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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C12orf65 - chromosome 12 open reading frame 65 | ||||||
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There are no transcripts associated with this gene. |
CDK2AP1 - cyclin dependent kinase 2 associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270433.1 | 584 | Intron | NP_001257362.1 | |||
NM_001270434.1 | 584 | Intron | NP_001257363.1 | |||
NM_004642.3 | 584 | Missense Mutation | AAT,AGT | N,S 21 | NP_004633.1 |