Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613984 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FANCD2 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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FANCD2 - Fanconi anemia complementation group D2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001018115.2 | Intron | NP_001018125.1 | ||||
NM_001319984.1 | Intron | NP_001306913.1 | ||||
NM_033084.4 | Intron | NP_149075.2 |
FANCD2OS - FANCD2 opposite strand | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164839.1 | Intron | NP_001158311.1 | ||||
NM_173472.1 | Intron | NP_775743.1 | ||||
XM_011533330.2 | Intron | XP_011531632.1 | ||||
XM_011533331.2 | Intron | XP_011531633.1 |