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CGGCTCCATTCAGCTTCACGTCCTG[C/T]TGTAAAGGCCCCGGGGCCACAGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608841 MIM: 602779 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CPAMD8 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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CPAMD8 - C3 and PZP like, alpha-2-macroglobulin domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015692.2 | 5522 | Silent Mutation | CAA,CAG | Q,Q 1830 | NP_056507.2 | |
XM_011527917.1 | 5522 | Silent Mutation | CAA,CAG | Q,Q 1818 | XP_011526219.1 | |
XM_011527918.1 | 5522 | Silent Mutation | CAA,CAG | Q,Q 1830 | XP_011526220.1 | |
XM_011527919.1 | 5522 | Silent Mutation | CAA,CAG | Q,Q 1830 | XP_011526221.1 | |
XM_011527920.2 | 5522 | Silent Mutation | CAA,CAG | Q,Q 1830 | XP_011526222.1 | |
XM_011527921.2 | 5522 | Intron | XP_011526223.1 | |||
XM_011527922.1 | 5522 | Intron | XP_011526224.1 | |||
XM_011527923.1 | 5522 | Intron | XP_011526225.1 | |||
XM_011527924.2 | 5522 | Intron | XP_011526226.1 | |||
XM_011527925.1 | 5522 | Silent Mutation | CAA,CAG | Q,Q 1087 | XP_011526227.1 | |
XM_017026594.1 | 5522 | UTR 3 | XP_016882083.1 |
F2RL3 - F2R like thrombin/trypsin receptor 3 | ||||||
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There are no transcripts associated with this gene. |