Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609235 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
BRSK1 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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BRSK1 - BR serine/threonine kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032430.1 | 819 | Intron | NP_115806.1 | |||
XM_005259327.3 | 819 | Intron | XP_005259384.1 | |||
XM_011527395.2 | 819 | Intron | XP_011525697.2 |
TMEM150B - transmembrane protein 150B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085488.2 | 819 | Silent Mutation | TTG,TTT | L,F 199 | NP_001078957.1 | |
NM_001282011.1 | 819 | Silent Mutation | TTG,TTT | L,F 199 | NP_001268940.1 | |
XM_005258812.3 | 819 | Missense Mutation | XP_005258869.1 | |||
XM_011526850.2 | 819 | Intron | XP_011525152.1 | |||
XM_011526851.2 | 819 | Intron | XP_011525153.1 | |||
XM_011526852.2 | 819 | Missense Mutation | XP_011525154.1 | |||
XM_011526853.2 | 819 | Missense Mutation | XP_011525155.1 | |||
XM_011526854.2 | 819 | Missense Mutation | XP_011525156.1 | |||
XM_011526855.2 | 819 | Missense Mutation | XP_011525157.1 | |||
XM_011526856.2 | 819 | Missense Mutation | XP_011525158.1 | |||
XM_011526857.2 | 819 | Missense Mutation | XP_011525159.1 | |||
XM_017026667.1 | 819 | Missense Mutation | XP_016882156.1 | |||
XM_017026668.1 | 819 | Missense Mutation | XP_016882157.1 |
Set Membership: |
HapMap |