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TGCCCATCTCCCATTAATATACAGA[C/T]GTAAGCCATCAGGTGGTAGAGCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
12 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 |
---|---|---|
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 |
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 | 6035 | Missense Mutation | NP_001161221.1 | |||
NM_001297772.1 | 6035 | Missense Mutation | NP_001284701.1 | |||
NM_018417.5 | 6035 | Missense Mutation | NP_060887.2 | |||
XM_005245330.4 | 6035 | Intron | XP_005245387.1 | |||
XM_006711449.3 | 6035 | Intron | XP_006711512.1 | |||
XM_011509760.2 | 6035 | Missense Mutation | XP_011508062.1 | |||
XM_011509762.2 | 6035 | Missense Mutation | XP_011508064.1 | |||
XM_011509763.2 | 6035 | Missense Mutation | XP_011508065.1 | |||
XM_011509766.2 | 6035 | Intron | XP_011508068.1 | |||
XM_017001778.1 | 6035 | Intron | XP_016857267.1 |