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AGGCAGCTCCTCAGGAGAGAGAGGC[C/T]GACTTCTTTCCAGGTTGCTTGGTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 107271 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C11orf91 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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C11orf91 - chromosome 11 open reading frame 91 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166692.1 | 567 | Silent Mutation | TCA,TCG | S,S 189 | NP_001160164.1 | |
XM_017017053.1 | 567 | Silent Mutation | TCA,TCG | S,S 189 | XP_016872542.1 |
CD59 - CD59 molecule | ||||||
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There are no transcripts associated with this gene. |