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TCTATGGTAATGCGGTTGTAGGGGC[A/G]GGGGCGGGGGCGGGGCAGCTGCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616666 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PHF12 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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PHF12 - PHD finger protein 12 | ||||||
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There are no transcripts associated with this gene. |
SEZ6 - seizure related 6 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098635.1 | 2923 | Missense Mutation | CGC,TGC | R,C 965 | NP_001092105.1 | |
NM_001290202.1 | 2923 | Missense Mutation | CGC,TGC | R,C 840 | NP_001277131.1 | |
NM_178860.4 | 2923 | Missense Mutation | CGC,TGC | R,C 965 | NP_849191.3 | |
XM_011524315.1 | 2923 | Intron | XP_011522617.1 | |||
XM_011524317.2 | 2923 | Intron | XP_011522619.1 |