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GAAGAAGATGGAGTCCCAGGCTGCC[C/T]GGCTACAGAGCCTGGAGGGGCGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602386 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF212 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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ZNF212 - zinc finger protein 212 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012256.3 | 307 | Missense Mutation | CGG,TGG | R,W 61 | NP_036388.2 | |
XM_005250055.2 | 307 | Missense Mutation | CGG,TGG | R,W 101 | XP_005250112.2 | |
XM_011516581.2 | 307 | Missense Mutation | CGG,TGG | R,W 7 | XP_011514883.2 | |
XM_011516582.1 | 307 | Missense Mutation | CGG,TGG | R,W 7 | XP_011514884.1 | |
XM_017012646.1 | 307 | Missense Mutation | CGG,TGG | R,W 61 | XP_016868135.1 | |
XM_017012647.1 | 307 | Missense Mutation | CGG,TGG | R,W 58 | XP_016868136.1 | |
XM_017012648.1 | 307 | Missense Mutation | CGG,TGG | R,W 7 | XP_016868137.1 |