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CCATTTGAGGTGGTGGCAGAGAGGC[C/T]TGTGTCCTATGTGCAGACCTACACT
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1228 | Missense Mutation | CCT,CTT | P,L 122 | NP_055766.2 | |
NM_199450.2 | 1228 | Missense Mutation | CCT,CTT | P,L 122 | NP_955522.1 | |
NM_199451.2 | 1228 | Missense Mutation | CCT,CTT | P,L 122 | NP_955523.1 | |
NM_199452.3 | 1228 | Intron | NP_955524.3 | |||
XM_017015937.1 | 1228 | Missense Mutation | CCT,CTT | P,L 122 | XP_016871426.1 | |
XM_017015938.1 | 1228 | Intron | XP_016871427.1 | |||
XM_017015939.1 | 1228 | Intron | XP_016871428.1 | |||
XM_017015940.1 | 1228 | Intron | XP_016871429.1 | |||
XM_017015941.1 | 1228 | Intron | XP_016871430.1 |