Detailed topic list for MITOMAP Web

Results from ConfirmedMutations web retrieved at 07:04 (GMT)

Number of topics: 1

Results from CitingMitomap web retrieved at 07:04 (GMT)

Number of topics: 1

Results from MITOMAP web retrieved at 07:04 (GMT)

AllVariants
All Current Variants A summary of counts and frequencies generated dynamically from Mitomap's current sequence set Execute Search: : View all variants in Mitom...
BA1BS1Summary
ClinGenApproved Summary of Variants Meeting ClinGen Approved Frequency Criteria for BA1 and BS1 .data th, .data td { border: 1px solid #CCC; padding: 5px; }...
Benign
ClinGenApproved Variants Meeting ClinGen Approved Frequency Criteria for BA1 and BS1 BA1 ( = 1%), total: 458 (Benign: 458); BS1 (0.5 Report date: 2024 03 22 F...
BenignTBD
ClinGenApproved Variants Meeting Frequency Criteria for BA1 and BS1 but Queued for Deeper Curation(currently not classified or classified as VUS) BA1 frequency ( ...
CambridgeReanalysis
Reanalysis of the Cambridge reference sequence by resequencing the original placental mtDNA sample Table from Andrews etal (1999), with permission of the authors....
CitingMitomap
MITOMAP A human mitochondrial genome database Please use one of the following two formats to cite MITOMAP * MITOMAP: A Human Mitochondrial Genome Database. htt...
ClinGenApproved
ClinGenApproved Variants Meeting ClinGen Approved Frequency Criteria for BA1 and BS1 BA1 ( = 1%), total: 458 (Benign: 458); BS1 (0.5 Report date: 2024 03 22 F...
ClinGenApproved-2021-01-15
ClinGenApproved Variants meeting ClinGen approved frequency criteria for BA1 and BS1 BA1 ( = 1%), total: 555 (Benign: 555); BS1 (0.5 Report date: 2021 07 09 l...
ClinGenApproved-V1
ClinGenApproved Variants meeting ClinGen approved frequency criteria for BA1 and BS1 BA1 ( = 1%), total: 528 (Benign: 528); BS1 (0.5 Report date: 2021 05 19 l...
ClinGenApproved1
ClinGenApproved Variants meeting ClinGen approved frequency criteria for BA1 and BS1 BA1 ( = 1%), total: 530 (benign: 530); BS1 (0.5 Report date: 2021 05 18 l...
ClinGenApproved2
ClinGenApproved Variants Meeting ClinGen Approved Frequency Criteria for BA1 and BS1 BA1 ( = 1%), total: 552 (Benign: 552); BS1 (0.5 Report date: 2022 11 03 l...
ClinGenApprovedOld
ClinGenApproved Variants meeting ClinGen approved frequency criteria for BA1 and BS1 BA1: = 1%, total: 414; BS1: 0.05 Report date: 2020 07 02 loading data......
ClinicalPhenotypes1
Clinical Phenotypes (non LHON) Associated with mtDNA Polypeptide Gene Mutations Reported in the Literature Syndromes Locus Disease* Allele ...
ClinicalPhenotypesPolypeptide
Reported Mitochondrial DNA Polypeptide Gene Disease Mutations, Non LHON Last update: March 2012 Panel A: The Top Pathogenic mtDNA Polypeptide Missense Mutations, ...
ClinicalPhenotypesRNA
Clinical Phenotypes Associated with mtDNA rRNA tRNA Mutations, Non LHON Last update: March 2012 The Top mtDNA Protein Synthesis (rRNA tRNA) Gene Mutations Sy...
ComplexRearrangements
MITOMAP: mtDNA Complex Rearrangements Last Edited: Nov 21, 2003 th { text align: center; } #gb footer { font size: 12px; } .mark { color: red; } #gb foot...
ComplexRearrangementsIE
MITOMAP: mtDNA Complex Rearrangements Last Edited: Nov 21, 2003 Parental Molecule Insert Size (bp) Apparent mtDNA Species Insert (nt) Flanking Repeats ...
ComplexRearrangementsTemplate
MITOMAP: mtDNA Complex Rearrangements Last Edited: MM:EditDate:MM Parental Molecule Insert Size (bp) Apparent mtDNA Species Insert (nt) Flanking Repeats...
ConfirmedCriteria
Criteria for Assessment of Variant Pathogenicity For Mitomap to assign a status of "Cfrm" to a possibly pathogenic variant, we look for confirming reports which a...
ConfirmedMutations
Report date: 2024 03 22 Mitomap's Confirmed Pathogenic Mutations td { padding left: 5px; padding right: 5px; } For more details, including current freque...
ConfirmedMutationsArchived
Mitomap's Confirmed Pathogenic Mutations For more details, including current frequencies and available sequences, see * Coding and Control Region Cfrm Mutation...
ConfirmedMutationsBak
Mitomap's Confirmed Pathogenic Mutations For more details, including current frequencies and available sequences, see * Coding and Control Region Cfrm Mutation...
ContinentVariants
MITOMAP: Common Continent Specific mtDNA Variants Last Edited: Jun 01, 2003 th { text align: center; } #gb footer { font size: 12px; } .mark { color: red...
ContinentVariantsIE
MITOMAP: Common Continent Specific mtDNA Variants Last Edited: Jun 01, 2003 Haplogroup Continent mtDNA Variants Continental mtDNA "AFRICA","L","3592 Hp...
ContinentVariantsTemplate
MITOMAP: Common Continent Specific mtDNA Variants Last Edited: MM:EditDate:MM Haplogroup Continent mtDNA Variants Continental mtDNA MM:TableData:MM Note...
DeletionsMultiple
MITOMAP: Reported Multiple mtDNA Deletions Within Individuals Last Edited: May 25, 2012 th { text align: center; } #gb footer { font size: 12px; } .mark { ...
DeletionsMultipleIE
MITOMAP: Reported Multiple mtDNA Deletions Within Individuals Last Edited: May 25, 2012 Deletion Junction (nt:nt) Deletion Size(bp) Repeat Type Repeat Loc...
DeletionsMultipleTemplate
MITOMAP: Reported Multiple mtDNA Deletions Within Individuals Last Edited: MM:EditDate:MM Deletion Junction (nt:nt) Deletion Size(bp) Repeat Type Repeat L...
DeletionsSingle
MITOMAP: Reported mtDNA Deletions Last Edited: Mar 21, 2024 th { text align: center; } #gb footer { font size: 12px; } .mark { color: red; } #gb footer ....
DeletionsSingleIE
MITOMAP: Reported mtDNA Deletions Last Edited: Mar 21, 2024 Deletion Junction (nt:nt) Deletion Size (bp) Repeat Location (nt) Repeat Type More Info "1...
DeletionsSingleTemplate
MITOMAP: Reported mtDNA Deletions Last Edited: MM:EditDate:MM Deletion Junction (nt:nt) Deletion Size (bp) Repeat Location (nt) Repeat Type More Info ...
DiseaseList
MITOMAP Disease Listing / Allele Classification with links to OMIM AD: Alzheimer's Disease ADPD: Alzheimer's Disease and Parkinsons's Disease AMDF: Ataxia, M...
GBFreqInfo
GenBank Frequency Information The current GenBank frequency data in our variant tables is derived from 61,134 human mitochondrial DNA sequences with size greater ...
GBFreqInfo-2019-05-01
GenBank Frequency Information The current GenBank frequency data in our variant tables is derived from 48,882 human mitochondrial DNA sequences with size greater ...
GBFreqInfo-2021-01-15
GenBank Frequency Information The current GenBank frequency data in our variant tables is derived from 51,836 human mitochondrial DNA sequences with size greater ...
GBFreqInfo-2022-01-15
GenBank Frequency Information The current GenBank frequency data in our variant tables is derived from 54,594 human mitochondrial DNA sequences with size greater ...
GenbankInfo
2021 Update #1: On Jan 15, 2021 we added 164 new full length (FL) and 206 new control region (CR) GenBank sequences to our database. This brings our total number ...
GenbankUpdate
2024 Update #1: On January 16, 2024 we added 566 new full length (FL) and 830 new control region (CR) GenBank sequences to our database. However, we also increase...
GenomeLoci
MITOMAP: Mitochondrial DNA Function Locations Last Edited: Jul 12, 2023 th { text align: center; } #gb footer { font size: 12px; } .mark { color: red; } ...
GenomeLociIE
MITOMAP: Mitochondrial DNA Function Locations Last Edited: Jul 12, 2023 Map Locus Starting Ending Shorthand Description Reference "MT HV2",57,372,"C...
GenomeLociTemplate
MITOMAP: Mitochondrial DNA Function Locations Last Edited: MM:EditDate:MM Map Locus Starting Ending Shorthand Description Reference MM:TableData:MM ...
HaplogrepLink
PhyloTree Markers
HaplogroupFreqs
Estimated Worldwide Haplotype Frequencies (%) Compiled by O. Derbeneva 2009 Please note: These numbers are simple means for published frequencies, not always have...
HaplogroupInfo
Haplogroup Information
HaplogroupMarkers
To search this page for a position of interest, use your browser's search function, Ctrl F (Windows) or ? Command F (Mac). Report date: 2023 06 15 Top Level ...
HaplogroupMarkers2009
Estimated Worldwide Haplotype Frequencies (%) Compiled for Mitomap by O. Derbeneva 2009 Please note: These numbers are for illustrative purposes, not for solid c...
HaplogroupMarkersLtrNumLtr
Download data Markers Found at 80% in Haplogroups (Ltr Num Ltr Level) Data retrieved from sequences collected from Genbank on 2024 1 26Number of unique vari...
HiFreqHGcalc
High Frequency Haplogroup (HFHG) Flags: Calculation Criteria For full length (FL) or control region (CR) sequences, the following conditions are applied to fla...
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Topic revision: 15 Sep 2015, UnknownUser
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