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GGACGCCATTCACCCCGATTCCAAG[C/T]ACCACATCATCCTTCATCTTGAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610999 | ||||||||||||||||||||
Literature Links: |
EPC1 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 |
EPC1 - enhancer of polycomb homolog 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272004.1 | 2340 | Silent Mutation | NP_001258933.1 | |||
NM_001272019.2 | 2340 | Silent Mutation | NP_001258948.1 | |||
NM_001282391.1 | 2340 | Silent Mutation | NP_001269320.1 | |||
NM_025209.3 | 2340 | Silent Mutation | NP_079485.1 | |||
XM_006717510.1 | 2340 | Silent Mutation | XP_006717573.1 |