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ATCGTTTTGATGGATATATCTTCCT[C/T]GACAGCAAAGGTTGGATTATTGGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605530 | ||||||||||||||||||||
Literature Links: |
MIR4502 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 |
MIR4502 - microRNA 4502 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
UPF3A - UPF3 regulator of nonsense transcripts homolog A (yeast) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023011.3 | 467 | Silent Mutation | CTC,CTT | L,L 137 | NP_075387.1 | |
NM_080687.2 | 467 | Silent Mutation | CTC,CTT | L,L 137 | NP_542418.1 | |
XM_005266202.4 | 467 | Intron | XP_005266259.1 | |||
XM_006719991.3 | 467 | Intron | XP_006720054.1 | |||
XM_011534844.1 | 467 | Intron | XP_011533146.1 | |||
XM_011534845.2 | 467 | Intron | XP_011533147.1 | |||
XM_011534846.1 | 467 | Silent Mutation | CTC,CTT | L,L 137 | XP_011533148.1 | |
XM_011534847.2 | 467 | UTR 5 | XP_011533149.1 | |||
XM_011534848.2 | 467 | Intron | XP_011533150.1 | |||
XM_017020709.1 | 467 | Intron | XP_016876198.1 | |||
XM_017020710.1 | 467 | Intron | XP_016876199.1 | |||
XM_017020711.1 | 467 | Intron | XP_016876200.1 | |||
XM_017020712.1 | 467 | Silent Mutation | CTC,CTT | L,L 137 | XP_016876201.1 |