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GCTGTGGCAGCATCGCTTTTTGCCC[A/G]AGCAGTCTGAGTCCTTGTGACACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602905 MIM: 605161 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNS1 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KCNS1 - potassium voltage-gated channel modifier subfamily S member 1 | ||||||
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There are no transcripts associated with this gene. |
WFDC5 - WAP four-disulfide core domain 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145652.3 | 397 | Missense Mutation | TCG,TTG | S,L 103 | NP_663627.1 | |
XM_011528601.1 | 397 | Missense Mutation | TCG,TTG | S,L 103 | XP_011526903.1 | |
XM_011528602.1 | 397 | Missense Mutation | TCG,TTG | S,L 103 | XP_011526904.1 |