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GCCTCGGGCCGGGGTCTTGGCGCCC[A/G]CTGCATGGTTGCGCTGGTGCTTGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613914 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF746 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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ZNF746 - zinc finger protein 746 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163474.1 | 2170 | Missense Mutation | GCG,GTG | A,V 591 | NP_001156946.1 | |
NM_152557.4 | 2170 | Missense Mutation | GCG,GTG | A,V 590 | NP_689770.3 | |
XM_005249955.2 | 2170 | Missense Mutation | GCG,GTG | A,V 606 | XP_005250012.1 | |
XM_005249956.2 | 2170 | Missense Mutation | GCG,GTG | A,V 605 | XP_005250013.1 | |
XM_005249957.1 | 2170 | Missense Mutation | GCG,GTG | A,V 593 | XP_005250014.1 | |
XM_011515838.1 | 2170 | Missense Mutation | GCG,GTG | A,V 578 | XP_011514140.1 |