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TATTCATTGTTGCATGAAAACAGGG[A/C]CAAGATTGGTTGGCAGATCTCCAGT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608260 | |||||||||||||||||||||||
Literature Links: |
KCNH8 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
KCNH8 - potassium voltage-gated channel subfamily H member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144633.2 | Intron | NP_653234.2 | ||||
XM_011533347.2 | Intron | XP_011531649.1 | ||||
XM_017005698.1 | Intron | XP_016861187.1 | ||||
XM_017005699.1 | Intron | XP_016861188.1 | ||||
XM_017005700.1 | Intron | XP_016861189.1 | ||||
XM_017005701.1 | Intron | XP_016861190.1 | ||||
XM_017005702.1 | Intron | XP_016861191.1 |