Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616196 MIM: 610815 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCAF13 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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DCAF13 - DDB1 and CUL4 associated factor 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015420.6 | 23 | Missense Mutation | CCA,CTA | P,L 108 | NP_056235.4 |
SLC25A32 - solute carrier family 25 member 32 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030780.4 | 23 | UTR 5 | NP_110407.2 | |||
XM_017013877.1 | 23 | Intron | XP_016869366.1 |
Set Membership: |
HapMap |