Search Thermo Fisher Scientific
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TGTAACAAGCCACGGTGATCACGAA[A/C]GGGATGAGGAACAGCAGGATGAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300525 | ||||||||||||||||||||
Literature Links: |
P2RY8 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 |
P2RY8 - purinergic receptor P2Y8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178129.4 | 980 | Silent Mutation | CCG,CCT | P,P 205 | NP_835230.1 | |
XM_005274429.3 | 980 | Silent Mutation | CCG,CCT | P,P 205 | XP_005274486.1 | |
XM_006724443.3 | 980 | Silent Mutation | CCG,CCT | P,P 394 | XP_006724506.2 | |
XM_011546178.2 | 980 | Silent Mutation | CCG,CCT | P,P 205 | XP_011544480.1 | |
XM_011546179.2 | 980 | Silent Mutation | CCG,CCT | P,P 205 | XP_011544481.1 |