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AGCCTCTCCCGAGTCTCCGCCCTGC[A/C]TCGCCCACAAATGCTCCAGCCCACG
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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
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 | 136 | Silent Mutation | GCA,GCC | A,A 70 | 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 | 136 | UTR 5 | NP_110407.2 | |||
XM_017013877.1 | 136 | UTR 5 | XP_016869366.1 |