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TTGCCAATGCTCAGATGGAGAACTG[C/T]GCCATCATTTACTGCAACGACGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608168 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNH6 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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KCNH6 - potassium voltage-gated channel subfamily H member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278919.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | NP_001265848.1 | |
NM_001278920.1 | 197 | UTR 5 | NP_001265849.1 | |||
NM_030779.3 | 197 | Silent Mutation | TGC,TGT | C,C 39 | NP_110406.1 | |
NM_173092.2 | 197 | Silent Mutation | TGC,TGT | C,C 39 | NP_775115.1 | |
XM_011525308.2 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_011523610.1 | |
XM_011525309.2 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_011523611.1 | |
XM_011525310.2 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_011523612.1 | |
XM_011525311.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_011523613.1 | |
XM_011525312.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_011523614.1 | |
XM_011525313.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_011523615.1 | |
XM_017025175.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_016880664.1 | |
XM_017025176.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_016880665.1 | |
XM_017025177.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_016880666.1 | |
XM_017025178.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_016880667.1 | |
XM_017025179.1 | 197 | Silent Mutation | TGC,TGT | C,C 39 | XP_016880668.1 | |
XM_017025180.1 | 197 | UTR 5 | XP_016880669.1 |