Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGATGTGGCTGATCTGCTGCAGTGT[C/G]GGTTTCGGGCACTGCAGGAACAAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605310 MIM: 164177 MIM: 600912 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCHCR1 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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CCHCR1 - coiled-coil alpha-helical rod protein 1 | ||||||
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There are no transcripts associated with this gene. |
POU5F1 - POU class 5 homeobox 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001173531.2 | 1483 | Silent Mutation | CCC,CCG | P,P 85 | NP_001167002.1 | |
NM_001285986.1 | 1483 | Silent Mutation | CCC,CCG | P,P 59 | NP_001272915.1 | |
NM_001285987.1 | 1483 | Silent Mutation | CCC,CCG | P,P 160 | NP_001272916.1 | |
NM_002701.5 | 1483 | Intron | NP_002692.2 | |||
NM_203289.5 | 1483 | Silent Mutation | CCC,CCG | P,P 85 | NP_976034.4 |
PSORS1C3 - psoriasis susceptibility 1 candidate 3 (non-protein coding) | ||||||
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There are no transcripts associated with this gene. |
TCF19 - transcription factor 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077511.1 | 1483 | Intron | NP_001070979.1 | |||
NM_001318908.1 | 1483 | Intron | NP_001305837.1 | |||
NM_007109.2 | 1483 | Intron | NP_009040.2 |