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TTGGGATTCAAGCCTACAGAACAGA[C/T]AGAAGTAGGAAAAGACAGTCTAAAA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607030 MIM: 608169 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GCA 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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GCA - grancalcin | ||||||
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There are no transcripts associated with this gene. |
KCNH7 - potassium voltage-gated channel subfamily H member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033272.3 | Intron | NP_150375.2 | ||||
NM_173162.2 | Intron | NP_775185.1 | ||||
XM_011512109.2 | Intron | XP_011510411.1 | ||||
XM_017005218.1 | Intron | XP_016860707.1 | ||||
XM_017005219.1 | Intron | XP_016860708.1 | ||||
XM_017005220.1 | Intron | XP_016860709.1 | ||||
XM_017005221.1 | Intron | XP_016860710.1 |
Set Membership: |
HapMap |