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Search Thermo Fisher Scientific
TAAGGCGAGAGGATCTGGCAAAGGC[C/G]TTTCCACATTCCTTACATTCATAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604751 | ||||||||||||||||||||
Literature Links: |
ZNF266 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ZNF266 - zinc finger protein 266 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271314.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | NP_001258243.1 | |
NM_006631.3 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | NP_006622.2 | |
XM_005259716.3 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_005259773.1 | |
XM_006722620.2 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_006722683.1 | |
XM_006722621.2 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_006722684.1 | |
XM_006722622.2 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_006722685.1 | |
XM_006722623.3 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_006722686.1 | |
XM_006722627.2 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_006722690.1 | |
XM_006722630.2 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_006722693.1 | |
XM_011527644.1 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_011525946.1 | |
XM_011527647.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_011525949.1 | |
XM_011527648.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_011525950.1 | |
XM_011527650.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_011525952.1 | |
XM_017026154.1 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_016881643.1 | |
XM_017026155.1 | 2020 | Missense Mutation | AAC,AAG | N,K 454 | XP_016881644.1 | |
XM_017026156.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881645.1 | |
XM_017026157.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881646.1 | |
XM_017026158.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881647.1 | |
XM_017026159.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881648.1 | |
XM_017026160.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881649.1 | |
XM_017026161.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881650.1 | |
XM_017026162.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881651.1 | |
XM_017026163.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881652.1 | |
XM_017026164.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881653.1 | |
XM_017026165.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881654.1 | |
XM_017026166.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881655.1 | |
XM_017026167.1 | 2020 | Missense Mutation | AAC,AAG | N,K 387 | XP_016881656.1 | |
XM_017026168.1 | 2020 | Missense Mutation | AAC,AAG | N,K 157 | XP_016881657.1 | |
XM_017026169.1 | 2020 | Missense Mutation | AAC,AAG | N,K 157 | XP_016881658.1 | |
XM_017026170.1 | 2020 | Missense Mutation | AAC,AAG | N,K 157 | XP_016881659.1 | |
XM_017026171.1 | 2020 | Missense Mutation | AAC,AAG | N,K 157 | XP_016881660.1 | |
XM_017026172.1 | 2020 | Missense Mutation | AAC,AAG | N,K 157 | XP_016881661.1 | |
XM_017026173.1 | 2020 | UTR 3 | XP_016881662.1 |