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GGGGTTTTCTGGGGGCTGGGGTCCT[A/G]CCGGCCAAGGGTCGTCAGGCCGGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605310 MIM: 613525 MIM: 613526 | ||||||||||||||||||||||||||||||||||||||
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. |
PSORS1C1 - psoriasis susceptibility 1 candidate 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014068.2 | 632 | Intron | NP_054787.2 |
PSORS1C2 - psoriasis susceptibility 1 candidate 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014069.2 | 632 | Missense Mutation | GCA,GTA | A,V 103 | NP_054788.2 |