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TCCCAGGTGATGAGGTCCAGAAGCC[A/G]GCTGGCGGGGTCATGGCAAAGCTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605416 MIM: 614460 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DKK3 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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DKK3 - dickkopf WNT signaling pathway inhibitor 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001018057.1 | 791 | Missense Mutation | CGG,TGG | R,W 247 | NP_001018067.1 | |
NM_013253.4 | 791 | Missense Mutation | CGG,TGG | R,W 247 | NP_037385.2 | |
NM_015881.5 | 791 | Missense Mutation | CGG,TGG | R,W 247 | NP_056965.3 | |
XM_006718178.2 | 791 | Missense Mutation | CGG,TGG | R,W 247 | XP_006718241.1 | |
XM_017017553.1 | 791 | Missense Mutation | CGG,TGG | R,W 247 | XP_016873042.1 | |
XM_017017554.1 | 791 | Missense Mutation | CGG,TGG | R,W 247 | XP_016873043.1 | |
XM_017017555.1 | 791 | Missense Mutation | CGG,TGG | R,W 247 | XP_016873044.1 |
USP47 - ubiquitin specific peptidase 47 | ||||||
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There are no transcripts associated with this gene. |