Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCCCGGAGCTTCCGGTGTTTCAGC[C/G]GCACCTGGCGGAACCTGTGGGAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602754 | ||||||||||||||||||||
Literature Links: |
KCNN4 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 |
KCNN4 - potassium calcium-activated channel subfamily N member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002250.2 | 1460 | Missense Mutation | CCG,CGG | P,R 355 | NP_002241.1 | |
XM_005258882.2 | 1460 | Missense Mutation | CCG,CGG | P,R 323 | XP_005258939.1 | |
XM_005258883.2 | 1460 | Missense Mutation | CCG,CGG | P,R 292 | XP_005258940.1 | |
XM_011526938.1 | 1460 | Intron | XP_011525240.1 |