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GTATTCCAGATATTTTGCTGTGATG[G/T]GTTCTTCAAGCTGAATTCCTCCACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609317 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM36 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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TRIM36 - tripartite motif containing 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017397.1 | 2668 | Intron | NP_001017397.1 | |||
NM_001017398.1 | 2668 | Intron | NP_001017398.1 | |||
NM_001300752.1 | 2668 | Missense Mutation | CAC,CCC | H,P 561 | NP_001287681.1 | |
NM_001300759.1 | 2668 | Missense Mutation | CAC,CCC | H,P 704 | NP_001287688.1 | |
NM_018700.3 | 2668 | Missense Mutation | CAC,CCC | H,P 716 | NP_061170.2 | |
XM_017009621.1 | 2668 | Missense Mutation | CAC,CCC | H,P 733 | XP_016865110.1 | |
XM_017009622.1 | 2668 | Missense Mutation | CAC,CCC | H,P 721 | XP_016865111.1 | |
XM_017009623.1 | 2668 | Intron | XP_016865112.1 |