Backlinks to Variants in MITOMAP Web (Search all webs)

Results from MITOMAP web retrieved at 12:07 (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 04 20 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 ( ...
ClinGenApproved
ClinGenApproved Variants Meeting ClinGen Approved Frequency Criteria for BA1 and BS1 BA1 ( = 1%), total: 458 (Benign: 458); BS1 (0.5 Report date: 2024 04 20 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...
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...
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...
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 ...
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...
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 ...
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...
HumanMitoReport
The Report of the Committee on the Human Mitochondrial Genome Adapted from the original print report: Wallace DC, Lott MT, Brown MD, Huoponen K, Torroni A 1995. R...
Indels
th, td { padding: 3px; border: solid 1px #CCC; } th { text align: center; } .even { background: #EEE; } Indel Variants Converted to Comply with HG...
LargeDeletions
Bibliography: Large Deletions in the Human mtDNA Abnet, C. C., Huppi, K., Carrera, A., Armistead, D., McKenney, K., Hu, N., Tang, Z. Z., Taylor, P. R. and Dawsey,...
MissingVariants
Patched Variants Index ID Position Refna Regna AlleleType NAChange AAChange Locus Phenotype Ethnicity 1 20100804015 896 A G polymorphism A G rRNA MT RNR1 2 201105...
MitoSeqs
Complete Mitochondrial DNA Sequences The revised Cambridge Reference Sequence (rCRS) is GenBank number NC_012920. Please use this new number when citing the rCRS ...
MitoSeqsBak
Complete Mitochondrial DNA Sequences The revised Cambridge Reference Sequence (rCRS) is GenBank number NC_012920. Please use this new number when citing the rCRS ...
MitoSites
MitoSites Mitochondrial Resources on the Web C. elegans Mitochondrial Directory (UK) Complex I Database (Scripps) DNA Polymerase Gamma Mutation Database EMPOP Co...
MitoTipInfo
MitoTIP An in silico tool for predicting pathogenicity of novel mitochondrial tRNA variants, developed by Neal Sondheimer and Sanjay Sonney (http://journals.plos....
Mitobank
MITOBANKMitochondrial DNA Sequences To submit unpublished mtDNA variant data to an online database, please contact lishen #64;chla.usc.edu at MSeqDR. To submit se...
MutationsCodingControl
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: Coding and Control Region Point Mutations Last Edited: Apr 17, 2024 The GB frequency data in Mitom...
MutationsCodingControlCfrm
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: Apr 17, 2024 For Mitomap to assign a...
MutationsCodingControlCfrmIE
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: Apr 17, 2024 For Mitomap to assign a...
MutationsCodingControlCfrmTemplate
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: MM:EditDate:MM For Mitomap to assign...
MutationsCodingControlIE
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: Coding and Control Region Point Mutations Last Edited: Apr 17, 2024 The GB frequency data in Mitom...
MutationsLHON
DIV.Section1 { page: Section1 } Leber's Hereditary Optic Neuropathy (LHON) Disease Mutations A. "Top 19" Primary LHON mutations, the first 3 mutations listed...
MutationsRNA
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: rRNA/tRNA mutations Last Edited: Apr 17, 2024 The GB frequency data in Mitomap is derived from 61...
MutationsRNACfrm
MITOMAP: Mitochondrial DNA Base Substitution Diseases:rRNA/tRNA Mutations with Cfrm Status Last Edited: Apr 17, 2024 For Mitomap to assign a status of "Cfrm" to a...
MutationsRNACfrmIE
MITOMAP: Mitochondrial DNA Base Substitution Diseases:rRNA/tRNA Mutations with Crfm Status Last Edited: Apr 17, 2024 For Mitomap to assign a status of "Cfrm" to ...
MutationsRNACfrmTemplate
MITOMAP: Mitochondrial DNA Base Substitution Diseases:rRNA/tRNA Mutations with Crfm Status Last Edited: MM:EditDate:MM For Mitomap to assign a status of "Cfrm" t...
MutationsRNAIE
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: rRNA/tRNA mutations Last Edited: Apr 17, 2024 The GB frequency data in Mitomap is derived from 61...
MutationsRNATemplate
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: rRNA/tRNA mutations Last Edited: MM:EditDate:MM The GB frequency data in Mitomap is derived from ...
NewUpdate
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...
NuclearGenesStructural
Structural Nuclear Genes for Mitochondrial Diseases Last update: January 2018 Complex Name OMIM Function Chromosome Inheritance Clinical Phenotype...
Polymorphisms
MITOMAP: Unpublished mtDNA Variants {ARCHIVED, no longer updated} Also see the submission index Point Mutations includes benign 'potentially pathogenic' var...
PolymorphismsCodingBlacklistIE
MITOMAP: mtDNA Coding Region RNA Sequence Variants (Blacklist) _Last Edited: , _ The GB frequency data is derived from 2200 GenBank sequences with size greate...
ReferenceList
References of Mitochondrial Interest This page is part of Mitomap. Date of last update: 5 January 2023. If you would like to submit published articles to be i...
ReferenceListAL
References of Mitochondrial Interest (A L) This page is part of Mitomap. Date of last update: 5 January 2023. If you would like to submit published articles t...
ReferenceListAL_archive
References of Mitochondrial Interest (A L) This page is part of Mitomap. Date of last update: 3 June 2019. If you would like to submit published articles to...
ReferenceListMZ
References of Mitochondrial Interest (M Z) This page is part of Mitomap. Date of last update: 08 December 2022. If you would like to submit published articles...
ReferenceListMZ_archive
References of Mitochondrial Interest (M Z) This page is part of Mitomap. Date of last update: 29 May 2019. If you would like to submit published articles to...
ReferenceList_archive
References of Mitochondrial Interest This page is part of Mitomap. Date of last update: 18 July 2019. If you would like to submit published articles to be i...
ReportRefs
References cited in The Report of the Committee on the Human Mitochondrial Genome 1a. Anderson, S., Bankier, A.T., Barrell, B.G., de Bruijn, M.H., Coulson, A.R., ...
SubmitUsingMitomaster
MITOMAP mtDNA Variant Submission New Process * The new process for submitting unpublished human mtDNA variants (point mutations, micro insertions, or micro d...
TestPage
MITOMAP A human mitochondrial genome database A compendium of polymorphisms and mutations of the human mitochondrial DNA The role of MITOMAP is to report...
ToolLaunchpad
New Tools! Look up Co variantsCompute frequencies of a variant with or without co occurence with another variant. Variant Search, aka "Marker Finder"Searc...
ToolLaunchpad2019
New Tools! * Variant Search, aka "Marker Finder" Search for variants found at specified frequencies in your choice of haplogroups or lineages originally deve...
ToolLaunchpadBak
New Tools! * Variant Search, aka "Marker Finder" Search for variants found at specified frequencies in your choice of haplogroups or lineages originally deve...
TopVariants
.p80 { background color:#ffff99; } .p50 { background color:#ccffff; } .p25 { background color:#ffebcd; } .head { text align: center; background co...
TopVariants42616
Report date: 04/02/18 View All Variants Most Frequent Variants in Mitomap ("Top 40") Analysis of 42,616 GenBank sequences, consisting of 5256 lineag...
TreeBibliography
Bibliography for MITOMAP's Large Phylogenetic Tree 9/25/2006 1, Mishmar D, Ruiz Pesini E, Golik P, Macaulay V, Clark AG, Hosseini S, Brandon M, Easley K, Ch...
UpdateHistory
2023 Update #2: On July 15, 2023 we added 1,779 new full length (FL) and 1,410 new control region (CR) GenBank sequences to our database. This brings our total nu...
VariantSubmissionCopyArchived
(function($) { $(function() { $("#unpublishedSubmittal").validate({ submitHandler: function(form) { var variantString = ''; var url = '/mitomaster/s...
VariantSubmissionList
MITOMAP: Unpublished mtDNA Variants {ARCHIVED, no longer updated} To submit unpublished mtDNA variant data to an online database, please contact lishen #64;chla.u...
VariantSubmissionTemplate
#variantinfo { border: 1px solid #DDD; } #variantinfo th, #variantinfo td { border: 1px solid #CCC; padding: 5px; } (function($) { $(function() { /...
VariantsCoding
MITOMAP: mtDNA Coding Region RNA Sequence Variants Last Edited: Mar 04, 2024 The GB frequency data is derived from 61124 GenBank sequences with size greater tha...
VariantsCodingIE
MITOMAP: mtDNA Coding Region RNA Sequence Variants Last Edited: Mar 04, 2024 The GB frequency data is derived from 61124 GenBank sequences with size greater th...
VariantsCodingPurged
MITOMAP: mtDNA Coding Region RNA Sequence Variants (revised sequence set March 2019) Last Edited: Apr 20, 2024 The GB frequency data is derived from 0 GenBank s...
VariantsCodingPurgedIE
MITOMAP: mtDNA Coding Region RNA Sequence Variants (revised sequence set March 2019) Last Edited: Apr 20, 2024 The GB frequency data is derived from 0 GenBank ...
VariantsCodingPurgedTemplate
MITOMAP: mtDNA Coding Region RNA Sequence Variants (revised sequence set March 2019) Last Edited: MM:EditDate:MM The GB frequency data is derived from MM:Genba...
VariantsCodingSupplement
MITOMAP: mtDNA Coding Region RNA Sequence Variants (Supplemental data: excluded sequences) Last Edited: Apr 20, 2024 The data in this table is derived from 0 Ge...
VariantsCodingSupplementIE
MITOMAP: mtDNA Coding Region RNA Sequence Variants (Supplemental data: excluded sequences) Last Edited: Apr 20, 2024 The data in this table is derived from 0 Ge...
VariantsCodingSupplementTemplate
MITOMAP: mtDNA Coding Region RNA Sequence Variants (Supplemental data: excluded sequences) Last Edited: MM:EditDate:MM The data in this table is derived from MM...
VariantsCodingTemplate
MITOMAP: mtDNA Coding Region RNA Sequence Variants Last Edited: MM:EditDate:MM The GB frequency data is derived from MM:GenbankCnt:MM GenBank sequences with si...
VariantsControl
MITOMAP: mtDNA Control Region Sequence Variants Last Edited: Mar 04, 2024 th { text align: center; } #gb footer { font size: 12px; } .mark { color: red; ...
VariantsControlIE
MITOMAP: mtDNA Control Region Sequence Variants Last Edited: Mar 04, 2024 Nucleotide Position Nucleotide Change GB Frequencytotal (FL/CR) Curated Referenc...
VariantsControlTemplate
MITOMAP: mtDNA Control Region Sequence Variants Last Edited: MM:EditDate:MM Nucleotide Position Nucleotide Change GB Frequencytotal (FL/CR) Curated Refere...
WebHome
MITOMAP A human mitochondrial genome database A compendium of polymorphisms and mutations in human mitochondrial DNA MITOMAP reports published data on human mito...
XClinicalPhenotypes2
Clinical Phenotypes (non LHON) Associated with mtDNA rRNA tRNA Mutations Reported in the Literature Syndromes Locus Disease* Allele RNA Ho* He* Status** Ref...
YorubanConversion
Yoruban to rCRS Conversion Human mitochondrial nucleotides are commonly identified using positions derived from the sequence first published by Anderson et al. an...
mitomap_error
MITOMAP Database Rebuild: September 13, 2012 15:01:52 Deleting old data Resetting sequences Loading the new data Rebuild finished MITOMAP Wiki Rebuild: Septembe...
Number of topics: 89
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