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CGGGGGTGCGGGAAGGCCACGGCGT[C/T]GCCCGCCCGGGCAATGTACTGGATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602216 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CBARP 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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CBARP - CACN beta subunit associated regulatory protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152769.2 | 1771 | Missense Mutation | AAC,GAC | N,D 365 | NP_689982.3 | |
XM_017026555.1 | 1771 | Missense Mutation | AAC,GAC | N,D 487 | XP_016882044.1 | |
XM_017026556.1 | 1771 | Missense Mutation | AAC,GAC | N,D 365 | XP_016882045.1 | |
XM_017026557.1 | 1771 | Missense Mutation | AAC,GAC | N,D 187 | XP_016882046.1 | |
XM_017026558.1 | 1771 | Missense Mutation | AAC,GAC | N,D 187 | XP_016882047.1 | |
XM_017026559.1 | 1771 | Missense Mutation | AAC,GAC | N,D 487 | XP_016882048.1 | |
XM_017026560.1 | 1771 | Intron | XP_016882049.1 | |||
XM_017026561.1 | 1771 | Intron | XP_016882050.1 | |||
XM_017026562.1 | 1771 | Intron | XP_016882051.1 |
STK11 - serine/threonine kinase 11 | ||||||
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There are no transcripts associated with this gene. |