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GGAGATATACTTCCCAATTCATCAG[A/T]TTATAAGTCCTCACTCATAGCACTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612515 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCAF17 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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DCAF17 - DDB1 and CUL4 associated factor 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164821.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | NP_001158293.1 | |
NM_025000.3 | 678 | Missense Mutation | GAT,GTT | D,V 116 | NP_079276.2 | |
XM_006712767.1 | 678 | Missense Mutation | GAT,GTT | D,V 29 | XP_006712830.1 | |
XM_006712768.1 | 678 | Missense Mutation | GAT,GTT | D,V 29 | XP_006712831.1 | |
XM_011511881.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_011510183.1 | |
XM_011511882.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_011510184.1 | |
XM_017004995.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_016860484.1 | |
XM_017004996.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_016860485.1 | |
XM_017004997.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_016860486.1 | |
XM_017004998.1 | 678 | UTR 5 | XP_016860487.1 | |||
XM_017004999.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_016860488.1 | |
XM_017005000.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_016860489.1 | |
XM_017005001.1 | 678 | Missense Mutation | GAT,GTT | D,V 116 | XP_016860490.1 | |
XM_017005002.1 | 678 | UTR 5 | XP_016860491.1 |