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CTTCCCAATAGGTCCACGTTATCTC[C/G]CAATAAGGATTTTTTCTCTAGTGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606949 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANAPC7 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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ANAPC7 - anaphase promoting complex subunit 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001137664.1 | 803 | Missense Mutation | CGA,GGA | R,G 268 | NP_001131136.1 | |
NM_016238.2 | 803 | Missense Mutation | CGA,GGA | R,G 268 | NP_057322.2 | |
XM_005253903.3 | 803 | Missense Mutation | CGA,GGA | R,G 47 | XP_005253960.1 | |
XM_011538454.2 | 803 | Missense Mutation | CGA,GGA | R,G 248 | XP_011536756.1 | |
XM_017019425.1 | 803 | Missense Mutation | CGA,GGA | R,G 268 | XP_016874914.1 | |
XM_017019426.1 | 803 | Missense Mutation | CGA,GGA | R,G 167 | XP_016874915.1 | |
XM_017019427.1 | 803 | Missense Mutation | CGA,GGA | R,G 167 | XP_016874916.1 | |
XM_017019428.1 | 803 | Missense Mutation | CGA,GGA | R,G 47 | XP_016874917.1 |