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CAAATGTCATACTGTGGTTTCTTAG[C/T]GCCGATAACGCCAGCTACCACTGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 103070 | ||||||||||||||||||||
Literature Links: |
ADCY8 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 |
ADCY8 - adenylate cyclase 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001115.2 | 3692 | Missense Mutation | ACT,GCT | T,A 1103 | NP_001106.1 | |
XM_005250769.3 | 3692 | Missense Mutation | ACT,GCT | T,A 1073 | XP_005250826.1 | |
XM_006716501.3 | 3692 | Missense Mutation | ACT,GCT | T,A 1037 | XP_006716564.1 | |
XM_017013006.1 | 3692 | Missense Mutation | ACT,GCT | T,A 1007 | XP_016868495.1 | |
XM_017013007.1 | 3692 | Intron | XP_016868496.1 |