Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGACTAGATGCGGACGGTGTTGATC[C/T]GCAGCGGCTGAACGTTCTTGCCATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 608353 MIM: 616755 | ||||||||||||||||||||
Literature Links: |
AZIN2 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 |
TRIM62 - tripartite motif containing 62 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018207.2 | 2044 | Missense Mutation | CAG,CGG | Q,R 469 | NP_060677.2 | |
XM_011541705.2 | 2044 | Missense Mutation | CAG,CGG | Q,R 348 | XP_011540007.1 | |
XM_017001629.1 | 2044 | Missense Mutation | CAG,CGG | Q,R 549 | XP_016857118.1 | |
XM_017001630.1 | 2044 | Missense Mutation | CAG,CGG | Q,R 538 | XP_016857119.1 | |
XM_017001631.1 | 2044 | Intron | XP_016857120.1 |