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AGAGCTCCAGCTTGCCCCTGAGGGC[A/G]GGGGTCATGGCGACCCGAGCTAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300916 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PNMA5 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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PNMA5 - paraneoplastic Ma antigen family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001103150.1 | 1239 | Silent Mutation | CCC,CCT | P,P 300 | NP_001096620.1 | |
NM_001103151.1 | 1239 | Silent Mutation | CCC,CCT | P,P 300 | NP_001096621.1 | |
NM_001184924.1 | 1239 | Silent Mutation | CCC,CCT | P,P 300 | NP_001171853.1 | |
NM_052926.2 | 1239 | Silent Mutation | CCC,CCT | P,P 300 | NP_443158.1 | |
XM_017029252.1 | 1239 | Silent Mutation | CCC,CCT | P,P 300 | XP_016884741.1 | |
XM_017029253.1 | 1239 | Silent Mutation | CCC,CCT | P,P 300 | XP_016884742.1 |