Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
53 submissions
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Phenotype: |
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Literature Links: |
JMJD4 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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JMJD4 - jumonji domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161465.1 | 252 | Missense Mutation | GCG,GTG | A,V 445 | NP_001154937.1 | |
NM_023007.2 | 252 | Missense Mutation | GCG,GTG | A,V 461 | NP_075383.2 | |
XM_011544262.2 | 252 | Missense Mutation | GCG,GTG | A,V 412 | XP_011542564.1 |
SNAP47 - synaptosome associated protein 47 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323930.1 | 252 | Intron | NP_001310859.1 | |||
NM_001323931.1 | 252 | Intron | NP_001310860.1 | |||
NM_001323932.1 | 252 | Intron | NP_001310861.1 | |||
NM_001323933.1 | 252 | Intron | NP_001310862.1 | |||
NM_001323934.1 | 252 | Intron | NP_001310863.1 | |||
NM_001323935.1 | 252 | Intron | NP_001310864.1 | |||
NM_053052.3 | 252 | Intron | NP_444280.2 | |||
XM_006711734.3 | 252 | Intron | XP_006711797.1 | |||
XM_017000231.1 | 252 | UTR 5 | XP_016855720.1 | |||
XM_017000232.1 | 252 | UTR 5 | XP_016855721.1 |
Set Membership: |
HapMap |