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You are here: Foswiki>MITOMAP/Submissions Web>AlleleExamples>VariantSubmission>VariantSubmissionList>20100212002 (29 Mar 2013, UnknownUser)
Unpublished Variant 20100212002
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: MalgorzataRydzanicz
- MITOMAP list of submitted variants
- MITOMASTER allele analysis
Citing this variant:
Rydzanicz, Malgorzata; Wr\xF3bel Maciej; Szyfter, Krzysztof 2010. MITOMAP mtDNA Sequence Data, https://mitomaster.mitomap.org/foswiki/bin/view/MITOMAP/Submissions/20100212002
VariantSubmissionForm edit
| LastName | Rydzanicz |
| FirstName | Malgorzata |
| MiddleName | |
| marydz@man.poznan.pl | |
| OrganizationName | Institute of Human Genetics, PAS |
| OrganizationURL | |
| Country | Poland |
| Address | |
| PILastName | Szyfter |
| PIFirstName | Krzysztof |
| PIMiddleName | |
| PIEmail | szyfkris@man.poznan.pl |
| OtherContributor | Wr\xF3bel Maciej |
| PolymorphismPosition | 16079 |
| Polymorphism | T |
| AlleleType | polymorphism |
| NAChange | C-T |
| AAChange | non-coding |
| Locus | Control Region |
| InsertPrePosition | |
| InsertPostPosition | |
| Insert | |
| DeletionPosition | |
| DeletionLength | |
| OtherAllele | |
| ComplexCategory | |
| Detection | automated |
| SampleID | G209 |
| Tissue | blood |
| Phenotype | Non-syndromic hearing loss |
| Ethnicity | Caucasian |
| Origin | Poland |
| Haplogroup | |
| Comment | D-loop |
Topic revision: r1 - 29 Mar 2013, UnknownUser
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