Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGAAGGTCTAGGTAGCTCACCACT[A/T]TCAATGCCAAATTGCACCCGGCGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
16 submissions
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Phenotype: |
MIM: 609973 MIM: 609712 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HCN3 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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HCN3 - hyperpolarization activated cyclic nucleotide gated potassium channel 3 | ||||||
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There are no transcripts associated with this gene. |
PKLR - pyruvate kinase, liver and RBC | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000298.5 | 1590 | Missense Mutation | GAA,GAT | E,D 538 | NP_000289.1 | |
NM_181871.3 | 1590 | Missense Mutation | GAA,GAT | E,D 507 | NP_870986.1 | |
XM_006711386.3 | 1590 | Missense Mutation | GAA,GAT | E,D 474 | XP_006711449.1 | |
XM_011509640.2 | 1590 | Missense Mutation | GAA,GAT | E,D 474 | XP_011507942.1 | |
XM_017001493.1 | 1590 | Intron | XP_016856982.1 |