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AGGGCTCAAATGATCCTCCTTCCTC[C/G]ACCTCCCAAGTAGCTAGAACTACAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607576 MIM: 609303 | ||||||||||||||||||||
Literature Links: |
CECR2 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 |
CECR2 - CECR2, histone acetyl-lysine reader | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SLC25A18 - solute carrier family 25 member 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303484.1 | Intron | NP_001290413.1 | ||||
NM_031481.2 | Intron | NP_113669.1 | ||||
XM_011546149.2 | Intron | XP_011544451.1 | ||||
XM_011546150.2 | Intron | XP_011544452.1 | ||||
XM_011546151.2 | Intron | XP_011544453.1 | ||||
XM_011546152.1 | Intron | XP_011544454.1 | ||||
XM_011546153.2 | Intron | XP_011544455.1 | ||||
XM_011546154.2 | Intron | XP_011544456.1 | ||||
XM_017028968.1 | Intron | XP_016884457.1 | ||||
XM_017028969.1 | Intron | XP_016884458.1 | ||||
XM_017028970.1 | Intron | XP_016884459.1 | ||||
XM_017028971.1 | Intron | XP_016884460.1 | ||||
XM_017028972.1 | Intron | XP_016884461.1 | ||||
XM_017028973.1 | Intron | XP_016884462.1 | ||||
XM_017028974.1 | Intron | XP_016884463.1 | ||||
XM_017028975.1 | Intron | XP_016884464.1 |