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ATGGCCCCGAGGCCTCCGACCGCCG[C/T]GCCCCAGGTGAGCAACGCGTTCCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609451 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZFP90 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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ZFP90 - ZFP90 zinc finger protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305203.1 | 318 | Missense Mutation | GCG,GTG | A,V 9 | NP_001292132.1 | |
NM_001305204.1 | 318 | Missense Mutation | GCG,GTG | A,V 9 | NP_001292133.1 | |
NM_001305206.1 | 318 | Missense Mutation | GCG,GTG | A,V 9 | NP_001292135.1 | |
NM_001305207.1 | 318 | Missense Mutation | GCG,GTG | A,V 9 | NP_001292136.1 | |
NM_001305208.1 | 318 | Missense Mutation | GCG,GTG | A,V 9 | NP_001292137.1 | |
NM_133458.3 | 318 | Missense Mutation | GCG,GTG | A,V 9 | NP_597715.2 | |
XM_005255804.2 | 318 | Missense Mutation | GCG,GTG | A,V 9 | XP_005255861.1 | |
XM_017022952.1 | 318 | Intron | XP_016878441.1 |