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TGGGGAGCAATGCATGGCAGAGATC[A/C]TCGTAGAACCGGAAACATGGGAATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610605 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CPEB2 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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CPEB2 - cytoplasmic polyadenylation element binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177381.1 | 114 | Missense Mutation | CAT,CCT | H,P 585 | NP_001170852.1 | |
NM_001177382.1 | 114 | Missense Mutation | CAT,CCT | H,P 585 | NP_001170853.1 | |
NM_001177383.1 | 114 | Missense Mutation | CAT,CCT | H,P 585 | NP_001170854.1 | |
NM_001177384.1 | 114 | Missense Mutation | CAT,CCT | H,P 585 | NP_001170855.1 | |
NM_182485.2 | 114 | Missense Mutation | CAT,CCT | H,P 585 | NP_872291.2 | |
NM_182646.2 | 114 | Missense Mutation | CAT,CCT | H,P 585 | NP_872587.2 | |
XM_005248135.3 | 114 | Missense Mutation | CAT,CCT | H,P 585 | XP_005248192.2 | |
XM_011513777.2 | 114 | Missense Mutation | CAT,CCT | H,P 585 | XP_011512079.1 | |
XM_011513778.2 | 114 | Missense Mutation | CAT,CCT | H,P 585 | XP_011512080.1 | |
XM_011513779.1 | 114 | Missense Mutation | CAT,CCT | H,P 585 | XP_011512081.1 | |
XM_017007733.1 | 114 | Missense Mutation | CAT,CCT | H,P 11 | XP_016863222.1 | |
XM_017007734.1 | 114 | Missense Mutation | CAT,CCT | H,P 11 | XP_016863223.1 |
CPEB2-AS1 - CPEB2 antisense RNA 1 (head to head) | ||||||
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There are no transcripts associated with this gene. |
LOC101929095 - uncharacterized LOC101929095 | ||||||
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There are no transcripts associated with this gene. |