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ATATTCCCCTGTGTTTCAGAGAGCC[G/T]CAAGGCTGTGTTCAGGAAGAGGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
MIM: 605205 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADCY10 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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ADCY10 - adenylate cyclase 10, soluble | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167749.2 | 6092 | Silent Mutation | NP_001161221.1 | |||
NM_001297772.1 | 6092 | Silent Mutation | NP_001284701.1 | |||
NM_018417.5 | 6092 | Silent Mutation | NP_060887.2 | |||
XM_005245330.4 | 6092 | Intron | XP_005245387.1 | |||
XM_006711449.3 | 6092 | Intron | XP_006711512.1 | |||
XM_011509760.2 | 6092 | Missense Mutation | XP_011508062.1 | |||
XM_011509762.2 | 6092 | Missense Mutation | XP_011508064.1 | |||
XM_011509763.2 | 6092 | Missense Mutation | XP_011508065.1 | |||
XM_011509766.2 | 6092 | Intron | XP_011508068.1 | |||
XM_017001778.1 | 6092 | Intron | XP_016857267.1 |