Search Thermo Fisher Scientific
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CACTCAGCAACATCCGTCTTTTTAG[A/G]TTCTTCAGTGTCTGAAAGAAAAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600385 | ||||||||||||||||||||
Literature Links: |
ADCY7 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 |
ADCY7 - adenylate cyclase 7 | ||||||
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There are no transcripts associated with this gene. |
BRD7 - bromodomain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001173984.2 | 2158 | Intron | NP_001167455.1 | |||
NM_013263.4 | 2158 | Intron | NP_037395.2 | |||
XM_011523046.2 | 2158 | Intron | XP_011521348.1 | |||
XM_011523047.2 | 2158 | Missense Mutation | CCT,TCT | P,S 655 | XP_011521349.1 | |
XM_011523048.2 | 2158 | Intron | XP_011521350.1 | |||
XM_011523049.2 | 2158 | Intron | XP_011521351.1 | |||
XM_011523050.2 | 2158 | Missense Mutation | CCT,TCT | P,S 437 | XP_011521352.1 | |
XM_017023179.1 | 2158 | Intron | XP_016878668.1 | |||
XM_017023180.1 | 2158 | Intron | XP_016878669.1 | |||
XM_017023181.1 | 2158 | Missense Mutation | CCT,TCT | P,S 436 | XP_016878670.1 |