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AGCGACCGGGCCCATTGTGCCGCGG[C/G]AGGAGGGGGCCGCGCGGGCGCCCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609236 | ||||||||||||||||||||
Literature Links: |
BRSK2 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 |
BRSK2 - BR serine/threonine kinase 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256627.1 | Intron | NP_001243556.1 | ||||
NM_001256629.1 | Intron | NP_001243558.1 | ||||
NM_001256630.1 | Intron | NP_001243559.1 | ||||
NM_001282218.1 | Intron | NP_001269147.1 | ||||
NM_003957.3 | Intron | NP_003948.2 | ||||
XM_005253218.3 | Intron | XP_005253275.1 | ||||
XM_006718374.2 | Intron | XP_006718437.1 | ||||
XM_006718376.2 | Intron | XP_006718439.1 | ||||
XM_011520461.2 | Intron | XP_011518763.1 | ||||
XM_011520462.2 | Intron | XP_011518764.1 | ||||
XM_017018532.1 | Intron | XP_016874021.1 | ||||
XM_017018533.1 | Intron | XP_016874022.1 | ||||
XM_017018534.1 | Intron | XP_016874023.1 | ||||
XM_017018535.1 | Intron | XP_016874024.1 | ||||
XM_017018536.1 | Intron | XP_016874025.1 | ||||
XM_017018537.1 | Intron | XP_016874026.1 | ||||
XM_017018538.1 | Intron | XP_016874027.1 |