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GCTGTTACCATACTGTAGGCTGGGG[A/G]GACCACAGTGGTTTGTTTCTGCAGC
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 |
---|---|---|
Global - Not Available | 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 |
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 | 3345 | Missense Mutation | CCC,TCC | P,S 1068 | NP_150375.2 | |
NM_173162.2 | 3345 | Intron | NP_775185.1 | |||
XM_011512109.2 | 3345 | Missense Mutation | CCC,TCC | P,S 1076 | XP_011510411.1 | |
XM_017005218.1 | 3345 | Missense Mutation | CCC,TCC | P,S 1073 | XP_016860707.1 | |
XM_017005219.1 | 3345 | Missense Mutation | CCC,TCC | P,S 1065 | XP_016860708.1 | |
XM_017005220.1 | 3345 | Missense Mutation | CCC,TCC | P,S 1061 | XP_016860709.1 | |
XM_017005221.1 | 3345 | Intron | XP_016860710.1 |