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GCAGCTCCTGATCACCCTGCCCACC[A/G]AGGCCAGCACCTGGGTGAAGTTGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
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Literature Links: |
ZFP69B 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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ZFP69B - ZFP69 zinc finger protein B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023070.2 | 364 | Missense Mutation | AAG,GAG | K,E 12 | NP_075558.2 | |
XM_005271136.1 | 364 | Missense Mutation | AAG,GAG | K,E 12 | XP_005271193.1 | |
XM_005271137.2 | 364 | Missense Mutation | AAG,GAG | K,E 12 | XP_005271194.1 | |
XM_005271138.3 | 364 | UTR 5 | XP_005271195.1 | |||
XM_005271139.3 | 364 | UTR 5 | XP_005271196.1 | |||
XM_017002147.1 | 364 | Missense Mutation | AAG,GAG | K,E 12 | XP_016857636.1 |