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TGAAGAGCACCAGAGCGGCCCAGAA[A/G]CAGATGTTGTCAAGGGCATTCCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 100725 MIM: 609426 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C17orf107 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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C17orf107 - chromosome 17 open reading frame 107 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145536.1 | 1404 | Intron | NP_001139008.1 |
CHRNE - cholinergic receptor nicotinic epsilon subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000080.3 | 1404 | Silent Mutation | TGC,TGT | C,C 458 | NP_000071.1 | |
XM_017024115.1 | 1404 | Silent Mutation | TGC,TGT | C,C 446 | XP_016879604.1 |
MINK1 - misshapen like kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024937.3 | 1404 | Intron | NP_001020108.1 | |||
NM_001321236.1 | 1404 | Intron | NP_001308165.1 | |||
NM_015716.4 | 1404 | Intron | NP_056531.1 | |||
NM_153827.4 | 1404 | Intron | NP_722549.2 | |||
NM_170663.4 | 1404 | Intron | NP_733763.1 | |||
XM_006721531.2 | 1404 | Intron | XP_006721594.1 | |||
XM_006721532.2 | 1404 | Intron | XP_006721595.1 | |||
XM_006721536.2 | 1404 | Intron | XP_006721599.1 | |||
XM_011523906.1 | 1404 | Intron | XP_011522208.1 | |||
XM_017024704.1 | 1404 | Intron | XP_016880193.1 | |||
XM_017024705.1 | 1404 | Intron | XP_016880194.1 | |||
XM_017024706.1 | 1404 | Intron | XP_016880195.1 | |||
XM_017024707.1 | 1404 | Intron | XP_016880196.1 | |||
XM_017024708.1 | 1404 | Intron | XP_016880197.1 |