Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGATTGGATGGCAGTTTGGAGCGCA[A/C]TGGCTCAGGCCTGGCCCCAGGTTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605206 | ||||||||||||||||||||
Literature Links: |
HCN4 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 |
HCN4 - hyperpolarization activated cyclic nucleotide gated potassium channel 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005477.2 | 4577 | Missense Mutation | GTG,TTG | V,L 1195 | NP_005468.1 | |
XM_011521148.2 | 4577 | Missense Mutation | GTG,TTG | V,L 789 | XP_011519450.1 |