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TGAAGCCCCTTTACTCGTCTTTCAG[C/T]GCATACAGCACATCATCCTGGCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 601902 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CC2D1B 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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CC2D1B - coiled-coil and C2 domain containing 1B | ||||||
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There are no transcripts associated with this gene. |
ORC1 - origin recognition complex subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190818.1 | 2694 | Silent Mutation | GCA,GCG | A,A 857 | NP_001177747.1 | |
NM_001190819.1 | 2694 | Silent Mutation | GCA,GCG | A,A 852 | NP_001177748.1 | |
NM_004153.3 | 2694 | Silent Mutation | GCA,GCG | A,A 857 | NP_004144.2 | |
XM_011541527.2 | 2694 | Silent Mutation | GCA,GCG | A,A 497 | XP_011539829.1 | |
XM_017001388.1 | 2694 | Silent Mutation | GCA,GCG | A,A 821 | XP_016856877.1 | |
XM_017001389.1 | 2694 | Silent Mutation | GCA,GCG | A,A 611 | XP_016856878.1 |
PLA2G12AP1 - phospholipase A2 group XIIA pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |