Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCGAAGCGGATCTTCACGAGGTCG[A/G]GCGGATGCAGCGCAAGGTTGGATAA
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 526 | UTR 5 | NP_056235.4 |
SLC25A32 - solute carrier family 25 member 32 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030780.4 | 526 | Missense Mutation | CCC,CTC | P,L 43 | NP_110407.2 | |
XM_017013877.1 | 526 | UTR 5 | XP_016869366.1 |