Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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)
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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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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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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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 | 1155 | Missense Mutation | ATG,GTG | M,V 211 | NP_001070979.1 | |
NM_001318908.1 | 1155 | Missense Mutation | ATG,GTG | M,V 211 | NP_001305837.1 | |
NM_007109.2 | 1155 | Missense Mutation | ATG,GTG | M,V 211 | NP_009040.2 |
Set Membership: |
HapMap |