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CTGCCGGCGGCCTCCAGTGCTGCGA[C/G]ACAACAGACATCTGTCGTTTAAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605529 | ||||||||||||||||||||
Literature Links: |
UPF2 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 |
UPF2 - UPF2 regulator of nonsense transcripts homolog (yeast) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015542.3 | Intron | NP_056357.1 | ||||
NM_080599.2 | Intron | NP_542166.1 | ||||
XM_011519449.2 | Intron | XP_011517751.1 | ||||
XM_017016034.1 | Intron | XP_016871523.1 |