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AAAACTGCGGAACTGTTGGAAGTTC[A/G]GGCAGCTTTTGTGCAGCTGACTCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607818 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC283045 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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LOC283045 - uncharacterized LOC283045 | ||||||
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There are no transcripts associated with this gene. |
ZNF365 - zinc finger protein 365 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014951.2 | 1456 | Missense Mutation | CAG,CGG | Q,R 198 | NP_055766.2 | |
NM_199450.2 | 1456 | Missense Mutation | CAG,CGG | Q,R 198 | NP_955522.1 | |
NM_199451.2 | 1456 | Missense Mutation | CAG,CGG | Q,R 198 | NP_955523.1 | |
NM_199452.3 | 1456 | Intron | NP_955524.3 | |||
XM_017015937.1 | 1456 | Missense Mutation | CAG,CGG | Q,R 198 | XP_016871426.1 | |
XM_017015938.1 | 1456 | Intron | XP_016871427.1 | |||
XM_017015939.1 | 1456 | Intron | XP_016871428.1 | |||
XM_017015940.1 | 1456 | Intron | XP_016871429.1 | |||
XM_017015941.1 | 1456 | Intron | XP_016871430.1 |