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AGTGCAGGATCCGGGTCCGGAGACC[C/T]CTCCGAGGGCTTGCCCCGAAGAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613317 MIM: 162080 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCAF11 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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DCAF11 - DDB1 and CUL4 associated factor 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163484.1 | 777 | Missense Mutation | CCC,CTC | P,L 16 | NP_001156956.1 | |
NM_025230.4 | 777 | Missense Mutation | CCC,CTC | P,L 16 | NP_079506.3 | |
NM_181357.2 | 777 | Missense Mutation | CCC,CTC | P,L 16 | NP_852002.1 |
NRL - neural retina leucine zipper | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006177.3 | 777 | Intron | NP_006168.1 | |||
XM_005267708.4 | 777 | Intron | XP_005267765.1 | |||
XM_005267709.3 | 777 | Intron | XP_005267766.1 | |||
XM_005267710.3 | 777 | Intron | XP_005267767.1 | |||
XM_011536801.2 | 777 | Intron | XP_011535103.2 | |||
XM_011536802.1 | 777 | Intron | XP_011535104.1 | |||
XM_011536804.2 | 777 | Intron | XP_011535106.1 | |||
XM_011536805.2 | 777 | Intron | XP_011535107.1 | |||
XM_011536806.2 | 777 | Intron | XP_011535108.2 | |||
XM_017021350.1 | 777 | Intron | XP_016876839.1 |