Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCAAGGCTGAGCTGATCCTGTACC[A/G]GAAGAGCGGTGAGGGGCCACCTGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604527 | ||||||||||||||||||||
Literature Links: |
KCNH3 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 |
KCNH3 - potassium voltage-gated channel subfamily H member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001314030.1 | 107 | Missense Mutation | CAG,CGG | Q,R 41 | NP_001300959.1 | |
NM_012284.2 | 107 | Missense Mutation | CAG,CGG | Q,R 101 | NP_036416.1 | |
XM_011538085.2 | 107 | Missense Mutation | CAG,CGG | Q,R 101 | XP_011536387.1 | |
XM_011538086.2 | 107 | Missense Mutation | CAG,CGG | Q,R 41 | XP_011536388.1 | |
XM_017019096.1 | 107 | Intron | XP_016874585.1 | |||
XM_017019097.1 | 107 | UTR 5 | XP_016874586.1 |