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TGCCAGCAGCTCGCGCAGCCTCTGT[G/T]TGGGAGTCTTGGTGAGCACGAAATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609555 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CPXM1 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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CPXM1 - carboxypeptidase X (M14 family), member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184699.1 | 1966 | Missense Mutation | NP_001171628.1 | |||
NM_019609.4 | 1966 | Missense Mutation | NP_062555.1 |