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TTTGGAGTCATAATTGTCATCTGGG[A/G]ATACTTATTTTGAGTTGTGTATCTT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615944 MIM: 611117 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
C2CD3 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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C2CD3 - C2 calcium dependent domain containing 3 | ||||||
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There are no transcripts associated with this gene. |
PPME1 - protein phosphatase methylesterase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271593.1 | Intron | NP_001258522.1 | ||||
NM_016147.2 | Intron | NP_057231.1 | ||||
XM_017017913.1 | Intron | XP_016873402.1 |
Set Membership: |
HapMap |