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CTCCTTGACAAACAGCTTCCTCTTT[A/G]GAAATGGCTTCACTCAGGTCCTGCA
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CCHCR1 - coiled-coil alpha-helical rod protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105563.1 | 2480 | Silent Mutation | TCC,TCT | S,S 812 | NP_001099033.1 | |
NM_001105564.1 | 2480 | Silent Mutation | TCC,TCT | S,S 848 | NP_001099034.1 | |
NM_019052.3 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | NP_061925.2 | |
XM_011514702.2 | 2480 | Silent Mutation | TCC,TCT | S,S 821 | XP_011513004.1 | |
XM_011514703.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_011513005.1 | |
XM_011514704.2 | 2480 | Silent Mutation | TCC,TCT | S,S 723 | XP_011513006.1 | |
XM_011514705.1 | 2480 | Silent Mutation | TCC,TCT | S,S 723 | XP_011513007.1 | |
XM_017010961.1 | 2480 | Silent Mutation | TCC,TCT | S,S 857 | XP_016866450.1 | |
XM_017010962.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866451.1 | |
XM_017010963.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866452.1 | |
XM_017010964.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866453.1 | |
XM_017010965.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866454.1 | |
XM_017010966.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866455.1 | |
XM_017010967.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866456.1 | |
XM_017010968.1 | 2480 | Silent Mutation | TCC,TCT | S,S 759 | XP_016866457.1 | |
XM_017010969.1 | 2480 | Silent Mutation | TCC,TCT | S,S 723 | XP_016866458.1 | |
XM_017010970.1 | 2480 | Silent Mutation | TCC,TCT | S,S 483 | XP_016866459.1 |
PSORS1C1 - psoriasis susceptibility 1 candidate 1 | ||||||
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There are no transcripts associated with this gene. |
PSORS1C2 - psoriasis susceptibility 1 candidate 2 | ||||||
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There are no transcripts associated with this gene. |