Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCCAGAAAATTGGGAGGACACCCT[C/T]GCTGATCCAAGAGCTCCAGCTTGCC
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 |
---|---|---|
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 |
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 | 1274 | Missense Mutation | CAA,CGA | Q,R 312 | NP_001096620.1 | |
NM_001103151.1 | 1274 | Missense Mutation | CAA,CGA | Q,R 312 | NP_001096621.1 | |
NM_001184924.1 | 1274 | Missense Mutation | CAA,CGA | Q,R 312 | NP_001171853.1 | |
NM_052926.2 | 1274 | Missense Mutation | CAA,CGA | Q,R 312 | NP_443158.1 | |
XM_017029252.1 | 1274 | Missense Mutation | CAA,CGA | Q,R 312 | XP_016884741.1 | |
XM_017029253.1 | 1274 | Missense Mutation | CAA,CGA | Q,R 312 | XP_016884742.1 |