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Search Thermo Fisher Scientific
CTCAAGGTGTTGAATCTTGGCGGCC[A/G]ATTGTACATTCATCTGTTTTAACCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611227 MIM: 609863 | ||||||||||||||||||||
Literature Links: |
HVCN1 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 |
HVCN1 - hydrogen voltage gated channel 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040107.1 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | NP_001035196.1 | |
NM_001256413.1 | 1319 | Missense Mutation | TCG,TTG | S,L 218 | NP_001243342.1 | |
NM_032369.3 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | NP_115745.2 | |
XM_005253948.2 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | XP_005254005.1 | |
XM_011538838.1 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_011537140.1 | |
XM_011538839.2 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_011537141.1 | |
XM_011538840.2 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_011537142.1 | |
XM_011538841.2 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_011537143.1 | |
XM_011538842.2 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_011537144.1 | |
XM_011538844.2 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_011537146.1 | |
XM_011538845.1 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | XP_011537147.1 | |
XM_011538846.2 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | XP_011537148.1 | |
XM_011538847.1 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | XP_011537149.1 | |
XM_017020026.1 | 1319 | Missense Mutation | TCG,TTG | S,L 285 | XP_016875515.1 | |
XM_017020027.1 | 1319 | Missense Mutation | TCG,TTG | S,L 238 | XP_016875516.1 |
TCTN1 - tectonic family member 1 | ||||||
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There are no transcripts associated with this gene. |