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ACTGAATTTTGAGAACACATTTCTT[C/T]GCCTAAAGCTAAATAACTTGGTATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612425 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SGO2 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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SGO2 - shugoshin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160033.1 | 656 | Missense Mutation | CGC,TGC | R,C 97 | NP_001153505.1 | |
NM_001160046.1 | 656 | Missense Mutation | CGC,TGC | R,C 97 | NP_001153518.1 | |
NM_152524.5 | 656 | Missense Mutation | CGC,TGC | R,C 97 | NP_689737.4 | |
XM_005246344.3 | 656 | Missense Mutation | CGC,TGC | R,C 112 | XP_005246401.2 | |
XM_005246345.3 | 656 | Missense Mutation | CGC,TGC | R,C 97 | XP_005246402.1 | |
XM_011510734.2 | 656 | Missense Mutation | CGC,TGC | R,C 97 | XP_011509036.1 | |
XM_017003452.1 | 656 | Missense Mutation | CGC,TGC | R,C 127 | XP_016858941.1 | |
XM_017003453.1 | 656 | Missense Mutation | CGC,TGC | R,C 127 | XP_016858942.1 | |
XM_017003454.1 | 656 | Missense Mutation | CGC,TGC | R,C 127 | XP_016858943.1 |