Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611933 MIM: 600328 MIM: 600346 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CISD3 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)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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CISD3 - CDGSH iron sulfur domain 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136498.1 | 337 | Missense Mutation | CGC,TGC | R,C 79 | NP_001129970.1 |
MLLT6 - MLLT6, PHD finger domain containing | ||||||
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There are no transcripts associated with this gene. |
PCGF2 - polycomb group ring finger 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007144.2 | 337 | Intron | NP_009075.1 | |||
XM_005257640.2 | 337 | Intron | XP_005257697.1 | |||
XM_005257641.4 | 337 | Intron | XP_005257698.1 | |||
XM_005257642.3 | 337 | Intron | XP_005257699.1 | |||
XM_017025016.1 | 337 | Intron | XP_016880505.1 |