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- SNP ID:
- rs142723260
- Gene
-
ADCY10 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 167878609 - 167878609 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CCTGGGTAGTACATCATCATCCTGG[C/T]AGCTAAGTTGACTTTTTGACCAATG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 605205
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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 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001167749.2 | 2882 | Missense Mutation | ACC,GCC | T,A 262 | NP_001161221.1 | |
| NM_001297772.1 | 2882 | Missense Mutation | ACC,GCC | T,A 323 | NP_001284701.1 | |
| NM_018417.5 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | NP_060887.2 | |
| XM_005245330.4 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | XP_005245387.1 | |
| XM_006711449.3 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | XP_006711512.1 | |
| XM_011509760.2 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | XP_011508062.1 | |
| XM_011509762.2 | 2882 | Missense Mutation | ACC,GCC | T,A 367 | XP_011508064.1 | |
| XM_011509763.2 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | XP_011508065.1 | |
| XM_011509766.2 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | XP_011508068.1 | |
| XM_017001778.1 | 2882 | Missense Mutation | ACC,GCC | T,A 415 | XP_016857267.1 | |
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