ClinVar Miner

List of variants in gene MT-TS2 studied for MELAS syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_012920.1(MT-TS2):m.12207G>A rs118203889
NC_012920.1(MT-TS2):m.12213G>A rs1603223616
NC_012920.1(MT-TS2):m.12215T>C rs1603223617
NC_012920.1(MT-TS2):m.12216C>T rs1603223618
NC_012920.1(MT-TS2):m.12217A>G rs1556424082
NC_012920.1(MT-TS2):m.12218C>A rs1603223621
NC_012920.1(MT-TS2):m.12223A>G rs1603223624
NC_012920.1(MT-TS2):m.12230A>G rs1603223625
NC_012920.1(MT-TS2):m.12231C>T rs1603223627
NC_012920.1(MT-TS2):m.12234A>G rs1603223628
NC_012920.1(MT-TS2):m.12235T>C rs1556424083
NC_012920.1(MT-TS2):m.12236G>A rs28359170
NC_012920.1(MT-TS2):m.12237C>T rs1603223632
NC_012920.1(MT-TS2):m.12239C>T rs376062400
NC_012920.1(MT-TS2):m.12241del rs1603223633
NC_012920.1(MT-TS2):m.12241dup rs1603223633
NC_012920.1(MT-TS2):m.12245T>C rs1603223634
NC_012920.1(MT-TS2):m.12246C>T rs28508189
NC_012920.1(MT-TS2):m.12247T>C rs1603223637
NC_012920.1(MT-TS2):m.12248A>G rs202114991
NC_012920.1(MT-TS2):m.12250C>T rs1603223639
NC_012920.1(MT-TS2):m.12255T>C rs1603223640
NC_012920.1(MT-TS2):m.12258C>T rs118203888
NC_012920.1(MT-TS2):m.12264C>T rs1603223642
NC_012920.1(MT-TS2):m.12265A>G rs1603223643

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.