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TCCCTGAGGCAGGAAAGGCTGTCCT[C/T]TGGGGAAAGGGAGAAGGAGATACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605222 | ||||||||||||||||||||
Literature Links: |
KCNMB3 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 |
KCNMB3 - potassium calcium-activated channel subfamily M regulatory beta subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163677.1 | 921 | Intron | NP_001157149.1 | |||
NM_014407.3 | 921 | Intron | NP_055222.3 | |||
NM_171828.2 | 921 | Intron | NP_741979.1 | |||
NM_171829.2 | 921 | Intron | NP_741980.1 | |||
NM_171830.1 | 921 | Silent Mutation | CAA,CAG | Q,Q 18 | NP_741981.1 |