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TACAGTTCTTGGTGGATGCAGTGAA[A/G]CCTTCGGCCTTTGCTGTGACCACAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CPXM2 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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CPXM2 - carboxypeptidase X (M14 family), member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198148.2 | 2011 | Silent Mutation | GGC,GGT | G,G 695 | NP_937791.2 | |
XM_005269528.3 | 2011 | Intron | XP_005269585.1 | |||
XM_011539283.2 | 2011 | Intron | XP_011537585.1 | |||
XM_011539285.2 | 2011 | Silent Mutation | GGC,GGT | G,G 586 | XP_011537587.1 | |
XM_011539286.1 | 2011 | Silent Mutation | GGC,GGT | G,G 468 | XP_011537588.1 | |
XM_017015673.1 | 2011 | Silent Mutation | GGC,GGT | G,G 586 | XP_016871162.1 | |
XM_017015674.1 | 2011 | Silent Mutation | GGC,GGT | G,G 368 | XP_016871163.1 |