Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610281 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZFP62 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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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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ZFP62 - ZFP62 zinc finger protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172638.1 | 2263 | Missense Mutation | AAG,AGG | K,R 698 | NP_001166109.1 | |
NM_152283.4 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | NP_689496.4 | |
XM_017009710.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865199.1 | |
XM_017009711.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865200.1 | |
XM_017009712.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865201.1 | |
XM_017009713.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865202.1 | |
XM_017009714.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865203.1 | |
XM_017009715.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865204.1 | |
XM_017009716.1 | 2263 | Missense Mutation | AAG,AGG | K,R 715 | XP_016865205.1 | |
XM_017009717.1 | 2263 | Missense Mutation | AAG,AGG | K,R 698 | XP_016865206.1 | |
XM_017009718.1 | 2263 | Missense Mutation | AAG,AGG | K,R 715 | XP_016865207.1 | |
XM_017009719.1 | 2263 | Missense Mutation | AAG,AGG | K,R 715 | XP_016865208.1 | |
XM_017009720.1 | 2263 | Missense Mutation | AAG,AGG | K,R 698 | XP_016865209.1 | |
XM_017009721.1 | 2263 | Missense Mutation | AAG,AGG | K,R 665 | XP_016865210.1 |
Set Membership: |
Validated |