Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCTGGATGCTGCCCTTGCGGCTTG[C/T]GGCTTCGTGTGCCAGCCCGATCACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 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 | |||
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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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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 | 1752 | Missense Mutation | ACA,GCA | T,A 372 | NP_060677.2 | |
XM_011541705.2 | 1752 | Missense Mutation | ACA,GCA | T,A 251 | XP_011540007.1 | |
XM_017001629.1 | 1752 | Missense Mutation | ACA,GCA | T,A 452 | XP_016857118.1 | |
XM_017001630.1 | 1752 | Missense Mutation | ACA,GCA | T,A 441 | XP_016857119.1 | |
XM_017001631.1 | 1752 | Intron | XP_016857120.1 |