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GTGAGCTGCAATTAAAGGATTTGAA[C/G]CTCTGTATACATTCAAAAGATTTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616841 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF468 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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ZNF468 - zinc finger protein 468 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008801.1 | 1026 | Intron | NP_001008801.1 | |||
NM_001277120.1 | 1026 | Intron | NP_001264049.1 | |||
XM_017027443.1 | 1026 | Missense Mutation | AGC,AGG | S,R 239 | XP_016882932.1 | |
XM_017027444.1 | 1026 | Missense Mutation | AGC,AGG | S,R 167 | XP_016882933.1 |