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CGTCATGCCTTACGTGGGAAGGACA[A/G]CAGTTCCAGGGGAAAGCTGCCATTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606030 MIM: 605813 | ||||||||||||||||||||
Literature Links: |
EDC4 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 |
EDC4 - enhancer of mRNA decapping 4 | ||||||
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There are no transcripts associated with this gene. |
NUTF2 - nuclear transport factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322038.1 | 594 | Silent Mutation | CAA,CAG | Q,Q 44 | NP_001308967.1 | |
NM_001322039.1 | 594 | Silent Mutation | CAA,CAG | Q,Q 44 | NP_001308968.1 | |
NM_001322040.1 | 594 | Silent Mutation | CAA,CAG | Q,Q 44 | NP_001308969.1 | |
NM_001322041.1 | 594 | Silent Mutation | CAA,CAG | Q,Q 44 | NP_001308970.1 | |
NM_005796.2 | 594 | Silent Mutation | CAA,CAG | Q,Q 44 | NP_005787.1 |