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TCCCCCTTTGCAGGATGCTCTGGCG[A/G]TTCATCTCCCTCTTCTCGGAGCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607740 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C17orf64 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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C17orf64 - chromosome 17 open reading frame 64 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181707.2 | 727 | Silent Mutation | CGA,CGG | R,R 114 | NP_859058.2 | |
XM_005257033.4 | 727 | Silent Mutation | CGA,CGG | R,R 147 | XP_005257090.1 | |
XM_005257034.4 | 727 | Silent Mutation | CGA,CGG | R,R 147 | XP_005257091.1 | |
XM_005257035.4 | 727 | Silent Mutation | CGA,CGG | R,R 77 | XP_005257092.1 | |
XM_005257036.2 | 727 | Silent Mutation | CGA,CGG | R,R 114 | XP_005257093.1 | |
XM_017024166.1 | 727 | Silent Mutation | CGA,CGG | R,R 77 | XP_016879655.1 |
RPL12P38 - ribosomal protein L12 pseudogene 38 | ||||||
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There are no transcripts associated with this gene. |
USP32 - ubiquitin specific peptidase 32 | ||||||
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There are no transcripts associated with this gene. |