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TCTGAGCCACTGCTAAATGCCTTCC[C/T]ACATTCATTACATTCATAGGGTTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611024 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF667 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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ZNF667 - zinc finger protein 667 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321355.1 | 1870 | Missense Mutation | AGG,GGG | R,G 504 | NP_001308284.1 | |
NM_001321356.1 | 1870 | Missense Mutation | AGG,GGG | R,G 561 | NP_001308285.1 | |
NM_022103.3 | 1870 | Missense Mutation | AGG,GGG | R,G 561 | NP_071386.3 | |
XM_011527208.1 | 1870 | Missense Mutation | AGG,GGG | R,G 561 | XP_011525510.1 | |
XM_011527209.1 | 1870 | Missense Mutation | AGG,GGG | R,G 561 | XP_011525511.1 |