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GGTATTTTATTAGTAGCCTGAAAAT[G/T]CCCCTAAAAAAAAAAAAAAACAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601182 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ORC2 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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ORC2 - origin recognition complex subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006190.4 | 1803 | Silent Mutation | GGA,GGC | G,G 490 | NP_006181.1 | |
XM_006712555.3 | 1803 | Silent Mutation | GGA,GGC | G,G 490 | XP_006712618.1 | |
XM_011511252.2 | 1803 | Silent Mutation | GGA,GGC | G,G 510 | XP_011509554.1 | |
XM_011511253.2 | 1803 | Silent Mutation | GGA,GGC | G,G 510 | XP_011509555.1 |