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GGTTTCATACCTGAGCAGCAAAGTC[A/G]GGGTTCTGGGCAAGCGTCTGCATCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 605440 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
UBQLN4 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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UBQLN4 - ubiquilin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304342.1 | 1280 | Intron | NP_001291271.1 | |||
NM_020131.4 | 1280 | Intron | NP_064516.2 | |||
XM_005245348.3 | 1280 | Silent Mutation | CCC,CCT | P,P 417 | XP_005245405.1 |