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CTCCCGCCTGACGTAGCGCGGCTTC[C/T]GTACTGAAACGGGTCAGAGACAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
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Literature Links: |
C1orf159 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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C1orf159 - chromosome 1 open reading frame 159 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017891.4 | 1342 | Missense Mutation | CAG,CGG | Q,R 169 | NP_060361.4 | |
XM_005244765.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 315 | XP_005244822.1 | |
XM_006710717.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 315 | XP_006710780.1 | |
XM_006710718.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 315 | XP_006710781.1 | |
XM_011541651.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539953.1 | |
XM_011541652.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539954.1 | |
XM_011541653.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539955.1 | |
XM_011541655.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539957.1 | |
XM_011541656.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539958.1 | |
XM_011541658.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539960.1 | |
XM_011541659.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539961.1 | |
XM_011541660.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_011539962.1 | |
XM_011541661.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 351 | XP_011539963.1 | |
XM_011541662.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 351 | XP_011539964.1 | |
XM_011541663.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 351 | XP_011539965.1 | |
XM_011541665.2 | 1342 | Missense Mutation | CAG,CGG | Q,R 315 | XP_011539967.1 | |
XM_017001572.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_016857061.1 | |
XM_017001573.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_016857062.1 | |
XM_017001574.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_016857063.1 | |
XM_017001575.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 383 | XP_016857064.1 | |
XM_017001576.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 351 | XP_016857065.1 | |
XM_017001577.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 315 | XP_016857066.1 | |
XM_017001578.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 315 | XP_016857067.1 | |
XM_017001579.1 | 1342 | UTR 3 | XP_016857068.1 | |||
XM_017001580.1 | 1342 | Missense Mutation | CAG,CGG | Q,R 237 | XP_016857069.1 |
RNF223 - ring finger protein 223 | ||||||
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There are no transcripts associated with this gene. |