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CAGGGGCAGCGGGGAGTCAGATCTC[A/C]GAGGAGAACACCAAGTTAAGGAGAC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601141 | |||||||||||||||||||||||
Literature Links: |
KCNAB1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
KCNAB1 - potassium voltage-gated channel subfamily A member regulatory beta subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308217.1 | 106 | Silent Mutation | TCA,TCC | S,S 14 | NP_001295146.1 | |
NM_001308222.1 | 106 | Intron | NP_001295151.1 | |||
NM_003471.3 | 106 | Intron | NP_003462.2 | |||
NM_172159.3 | 106 | Intron | NP_751891.1 | |||
NM_172160.2 | 106 | Silent Mutation | TCA,TCC | S,S 14 | NP_751892.1 | |
XM_011513115.2 | 106 | Intron | XP_011511417.1 | |||
XM_011513116.2 | 106 | Intron | XP_011511418.1 | |||
XM_011513117.2 | 106 | Intron | XP_011511419.1 | |||
XM_017007171.1 | 106 | Intron | XP_016862660.1 | |||
XM_017007172.1 | 106 | Intron | XP_016862661.1 | |||
XM_017007173.1 | 106 | Intron | XP_016862662.1 | |||
XM_017007174.1 | 106 | Silent Mutation | TCA,TCC | S,S 14 | XP_016862663.1 |