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You are here: Foswiki>MITOMAP/Submissions Web>AlleleExamples>VariantSubmission>VariantSubmissionList>20100204001 (29 Mar 2013, UnknownUser)
Unpublished Variant 20100204001
This is a record of an observed human mtDNA variant submitted to MITOMAP- Submitters may return to this page at any time to update the information. Submitters who wish to amend a record submitted before November 2009 must register and send an email to mitomap@email.chop.edu to obtain editing privileges on the page.
- Submitted by: NajlaMezghani
- MITOMAP list of submitted variants
- MITOMASTER allele analysis
Citing this variant:
mezghani, najla; fakhfakh, faiza 2010. MITOMAP mtDNA Sequence Data, https://mitomap.org/foswiki/bin/view/MITOMAP/Submissions/20100204001
VariantSubmissionForm edit
| LastName | mezghani |
| FirstName | najla |
| MiddleName | |
| najla_mezghani2@yahoo.fr | |
| OrganizationName | |
| OrganizationURL | |
| Country | Tunisia |
| Address | |
| PILastName | fakhfakh |
| PIFirstName | faiza |
| PIMiddleName | |
| PIEmail | faiza.fakhfakh@gnet.tn |
| OtherContributor | |
| PolymorphismPosition | 16328 |
| Polymorphism | G |
| AlleleType | polymorphism |
| NAChange | C-G |
| AAChange | non-coding |
| Locus | Control Region |
| InsertPrePosition | |
| InsertPostPosition | |
| Insert | |
| DeletionPosition | |
| DeletionLength | |
| OtherAllele | |
| ComplexCategory | |
| Detection | automated |
| SampleID | mit33 |
| Tissue | blood |
| Phenotype | diabetes;bilateral sensorineural hearing loss, mental and language disorder, bilateral cataract, retinitis pigmentosa, pyramidal syndrome with calcification of basal ganglia and epilepsy |
| Ethnicity | Tunisian |
| Origin | Tunisia |
| Haplogroup | |
| Comment |
Topic revision: r1 - 29 Mar 2013, UnknownUser
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