Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTAACTGAAACGAATTGGAGTAACT[C/G]AAGGATTTCCCACACTGTTTACATT
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
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
ZNF266 - zinc finger protein 266 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271314.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | NP_001258243.1 | |
NM_006631.3 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | NP_006622.2 | |
XM_005259716.3 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_005259773.1 | |
XM_006722620.2 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_006722683.1 | |
XM_006722621.2 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_006722684.1 | |
XM_006722622.2 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_006722685.1 | |
XM_006722623.3 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_006722686.1 | |
XM_006722627.2 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_006722690.1 | |
XM_006722630.2 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_006722693.1 | |
XM_011527644.1 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_011525946.1 | |
XM_011527647.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_011525949.1 | |
XM_011527648.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_011525950.1 | |
XM_011527650.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_011525952.1 | |
XM_017026154.1 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_016881643.1 | |
XM_017026155.1 | 2362 | Missense Mutation | TTC,TTG | F,L 568 | XP_016881644.1 | |
XM_017026156.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881645.1 | |
XM_017026157.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881646.1 | |
XM_017026158.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881647.1 | |
XM_017026159.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881648.1 | |
XM_017026160.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881649.1 | |
XM_017026161.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881650.1 | |
XM_017026162.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881651.1 | |
XM_017026163.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881652.1 | |
XM_017026164.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881653.1 | |
XM_017026165.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881654.1 | |
XM_017026166.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881655.1 | |
XM_017026167.1 | 2362 | Missense Mutation | TTC,TTG | F,L 501 | XP_016881656.1 | |
XM_017026168.1 | 2362 | Missense Mutation | TTC,TTG | F,L 271 | XP_016881657.1 | |
XM_017026169.1 | 2362 | Missense Mutation | TTC,TTG | F,L 271 | XP_016881658.1 | |
XM_017026170.1 | 2362 | Missense Mutation | TTC,TTG | F,L 271 | XP_016881659.1 | |
XM_017026171.1 | 2362 | Missense Mutation | TTC,TTG | F,L 271 | XP_016881660.1 | |
XM_017026172.1 | 2362 | Missense Mutation | TTC,TTG | F,L 271 | XP_016881661.1 | |
XM_017026173.1 | 2362 | UTR 3 | XP_016881662.1 |