Search Thermo Fisher Scientific
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TCTCGGGATGTCTCCAGAGATGCCT[C/T]CGACACCCCATCAATGCTGCTCAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602905 | ||||||||||||||||||||
Literature Links: |
KCNS1 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 |
KCNS1 - potassium voltage-gated channel modifier subfamily S member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322799.1 | 1877 | Missense Mutation | AAG,GAG | K,E 494 | NP_001309728.1 | |
NM_002251.4 | 1877 | Missense Mutation | AAG,GAG | K,E 494 | NP_002242.2 | |
XM_017027846.1 | 1877 | Missense Mutation | AAG,GAG | K,E 495 | XP_016883335.1 |