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TCCTGACTGGGGTCCTTCATTTTCC[A/C]TGAGCATTTCCACGCCATTCTGATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF438 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
|
ZNF438 - zinc finger protein 438 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143766.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | NP_001137238.1 | |
NM_001143767.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | NP_001137239.1 | |
NM_001143768.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | NP_001137240.1 | |
NM_001143769.1 | 2697 | Missense Mutation | AGG,ATG | R,M 692 | NP_001137241.1 | |
NM_001143770.1 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | NP_001137242.1 | |
NM_001143771.1 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | NP_001137243.1 | |
NM_182755.2 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | NP_877432.1 | |
XM_006717393.3 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_006717456.1 | |
XM_006717396.3 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_006717459.1 | |
XM_006717398.3 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | XP_006717461.1 | |
XM_006717399.3 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | XP_006717462.1 | |
XM_011519371.2 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_011517673.1 | |
XM_011519372.2 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_011517674.1 | |
XM_011519373.2 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_011517675.1 | |
XM_011519374.2 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_011517676.1 | |
XM_011519376.2 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | XP_011517678.1 | |
XM_011519377.2 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | XP_011517679.1 | |
XM_017015863.1 | 2697 | Missense Mutation | AGG,ATG | R,M 752 | XP_016871352.1 | |
XM_017015864.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871353.1 | |
XM_017015865.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871354.1 | |
XM_017015866.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871355.1 | |
XM_017015867.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871356.1 | |
XM_017015868.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871357.1 | |
XM_017015869.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871358.1 | |
XM_017015870.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871359.1 | |
XM_017015871.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871360.1 | |
XM_017015872.1 | 2697 | Missense Mutation | AGG,ATG | R,M 741 | XP_016871361.1 | |
XM_017015873.1 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | XP_016871362.1 | |
XM_017015874.1 | 2697 | Missense Mutation | AGG,ATG | R,M 731 | XP_016871363.1 | |
XM_017015875.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871364.1 | |
XM_017015876.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871365.1 | |
XM_017015877.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871366.1 | |
XM_017015878.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871367.1 | |
XM_017015879.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871368.1 | |
XM_017015880.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871369.1 | |
XM_017015881.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871370.1 | |
XM_017015882.1 | 2697 | Missense Mutation | AGG,ATG | R,M 305 | XP_016871371.1 |