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AATAGCAGAAAAGTCCTTGAGGTGC[C/T]TAAGGCCCAGGGCCGGGTGCCTCCG
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 152427 | ||||||||||||||||||||||||||
Literature Links: |
KCNH2 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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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 |
KCNH2 - potassium voltage-gated channel subfamily H member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000238.3 | 3575 | UTR 3 | NP_000229.1 | |||
NM_001204798.1 | 3575 | Intron | NP_001191727.1 | |||
NM_172056.2 | 3575 | Intron | NP_742053.1 | |||
NM_172057.2 | 3575 | UTR 3 | NP_742054.1 | |||
XM_011516185.2 | 3575 | UTR 3 | XP_011514487.1 | |||
XM_011516186.2 | 3575 | Intron | XP_011514488.1 | |||
XM_017012195.1 | 3575 | UTR 3 | XP_016867684.1 | |||
XM_017012196.1 | 3575 | UTR 3 | XP_016867685.1 |
Set Membership: |
HapMap |