Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
73 submissions
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Phenotype: |
MIM: 608192 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
C1orf112 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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C1orf112 - chromosome 1 open reading frame 112 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320047.1 | 2091 | Intron | NP_001306976.1 | |||
NM_001320048.1 | 2091 | Intron | NP_001306977.1 | |||
NM_001320050.1 | 2091 | Intron | NP_001306979.1 | |||
NM_001320051.1 | 2091 | Intron | NP_001306980.1 | |||
NM_018186.3 | 2091 | Intron | NP_060656.2 | |||
XM_005245317.4 | 2091 | Intron | XP_005245374.1 | |||
XM_011509735.2 | 2091 | Intron | XP_011508037.1 | |||
XM_017001722.1 | 2091 | Intron | XP_016857211.1 | |||
XM_017001723.1 | 2091 | Intron | XP_016857212.1 | |||
XM_017001724.1 | 2091 | Intron | XP_016857213.1 | |||
XM_017001725.1 | 2091 | Intron | XP_016857214.1 |
SCYL3 - SCY1 like pseudokinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020423.6 | 2091 | Silent Mutation | NP_065156.5 | |||
NM_181093.3 | 2091 | Silent Mutation | NP_851607.2 | |||
XM_006711465.1 | 2091 | Silent Mutation | XP_006711528.1 | |||
XM_011509801.1 | 2091 | Silent Mutation | XP_011508103.1 | |||
XM_011509802.1 | 2091 | Silent Mutation | XP_011508104.1 | |||
XM_011509803.1 | 2091 | Silent Mutation | XP_011508105.1 | |||
XM_017001862.1 | 2091 | Silent Mutation | XP_016857351.1 | |||
XM_017001863.1 | 2091 | Silent Mutation | XP_016857352.1 | |||
XM_017001864.1 | 2091 | Silent Mutation | XP_016857353.1 | |||
XM_017001865.1 | 2091 | Silent Mutation | XP_016857354.1 |
Set Membership: |
HapMap |