Backlinks to Benign in MITOMAP Web (Search all webs)

Results from MITOMAP web retrieved at 02:20 (GMT)

BA1BS1Summary
ClinGenApproved Summary of Variants Meeting ClinGen Approved Frequency Criteria for BA1 and BS1 .data th, .data td { border: 1px solid #CCC; padding: 5px; }...
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 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...
ConfirmedMutations
Report date: 2024 03 22 Mitomap's Confirmed Pathogenic Mutations td { padding left: 5px; padding right: 5px; } For more details, including current freque...
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 ...
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,...
MitoTipInfo
MitoTIP An in silico tool for predicting pathogenicity of novel mitochondrial tRNA variants, developed by Neal Sondheimer and Sanjay Sonney (http://journals.plos....
MitoTipScores
th, .range { text align: center; } th, td { padding left: 20px; padding right: 20px; } MitoTip Scores The current MitoTip scores are available for downloadi...
MutationsCodingControl
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: Coding and Control Region Point Mutations Last Edited: Mar 15, 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: Mar 15, 2024 For Mitomap to assign a...
MutationsCodingControlCfrmIE
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: Mar 15, 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: Mar 15, 2024 The GB frequency data in Mitom...
MutationsRNA
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: rRNA/tRNA mutations Last Edited: Mar 15, 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: Mar 15, 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: Mar 15, 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...
Polymorphisms
MITOMAP: Unpublished mtDNA Variants {ARCHIVED, no longer updated} Also see the submission index Point Mutations includes benign 'potentially pathogenic' var...
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...
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...
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...
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...
Number of topics: 28
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