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CTATCTTTGTTCACTGCCTTCTTGC[C/T]CTTGTGTAAGGGGCCAGCCGGGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600749 MIM: 604235 | ||||||||||||||||||||
Literature Links: |
CEBPE 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 |
CEBPE - CCAAT/enhancer binding protein epsilon | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001805.3 | 1106 | Missense Mutation | AGC,GGC | S,G 196 | NP_001796.2 |
SLC7A8 - solute carrier family 7 member 8 | ||||||
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There are no transcripts associated with this gene. |