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CGGTCCAGTGTTGAACTCTGTAGTA[A/G]ATCTGTGGGGGTTTTGCTGGGGGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604911 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CNOT4 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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CNOT4 - CCR4-NOT transcription complex subunit 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008225.2 | 2441 | Intron | NP_001008226.1 | |||
NM_001190847.1 | 2441 | Silent Mutation | CTA,TTA | L,L 633 | NP_001177776.1 | |
NM_001190848.1 | 2441 | Intron | NP_001177777.1 | |||
NM_001190849.1 | 2441 | Silent Mutation | CTA,TTA | L,L 701 | NP_001177778.1 | |
NM_001190850.1 | 2441 | Silent Mutation | CTA,TTA | L,L 704 | NP_001177779.1 | |
NM_013316.3 | 2441 | Silent Mutation | CTA,TTA | L,L 630 | NP_037448.2 | |
XM_017012235.1 | 2441 | Silent Mutation | CTA,TTA | L,L 704 | XP_016867724.1 |