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AGAAACCAGACACAAATGAAAATTC[C/T]GCCAAGTCACTCTTGAAATCCCACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614502 MIM: 614056 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C9orf116 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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C9orf116 - chromosome 9 open reading frame 116 | ||||||
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There are no transcripts associated with this gene. |
PPP1R26 - protein phosphatase 1 regulatory subunit 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014811.3 | 1608 | Intron | NP_055626.3 | |||
XM_005263411.2 | 1608 | Intron | XP_005263468.1 | |||
XM_017015355.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870844.1 | |
XM_017015356.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870845.1 | |
XM_017015357.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870846.1 | |
XM_017015358.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870847.1 | |
XM_017015359.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870848.1 | |
XM_017015360.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870849.1 | |
XM_017015361.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870850.1 | |
XM_017015362.1 | 1608 | Silent Mutation | TCC,TCT | S,S 259 | XP_016870851.1 |