List of variants reported as likely pathogenic for MELAS syndrome by Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.10406G>A	rs1603222826
NC_012920.1(MT-CYB):m.10408T>C	rs1603222827
NC_012920.1(MT-CYB):m.10460T>C	rs1603222848
NC_012920.1(MT-CYB):m.12148T>C	rs1603223571
NC_012920.1(MT-CYB):m.12258C>T	rs118203888
NC_012920.1(MT-CYB):m.12264C>T	rs1603223642
NC_012920.1(MT-CYB):m.12335T>C	rs1603223668
NC_012920.1(MT-CYB):m.16002T>C	rs1603225633
NC_012920.1(MT-CYB):m.1659T>C	rs1603218609
NC_012920.1(MT-CYB):m.3288A>G	rs1603218872
NC_012920.1(MT-CYB):m.4296G>A	rs1603219393
NC_012920.1(MT-CYB):m.4308G>A	rs1603219396
NC_012920.1(MT-CYB):m.4372C>T	rs1603219429
NC_012920.1(MT-CYB):m.4437C>T	rs1603219459
NC_012920.1(MT-CYB):m.578T>C	rs1603218446
NC_012920.1(MT-CYB):m.618T>C	rs1603218460
NC_012920.1(MT-CYB):m.8299G>A	rs1603221391
NC_012920.1(MT-ND1):m.1624C>T	rs199476144
NC_012920.1(MT-ND1):m.1630A>G	rs1603218588
NC_012920.1(MT-ND1):m.4142G>A	rs1603219317
NC_012920.1(MT-ND5):m.13046T>C	rs1603224015
NC_012920.1(MT-ND6):m.14465G>A	rs1603224738
NC_012920.1(MT-TD):m.7566G>A	rs1603221016
NC_012920.1(MT-TE):m.14674T>C	rs387906421
NC_012920.1(MT-TE):m.14709T>C	rs121434453
NC_012920.1(MT-TG):m.9997T>A	rs121434475
NC_012920.1(MT-TK):m.8319A>G	rs1603221401
NC_012920.1(MT-TL1):m.3252A>G	rs199474661
m.3242G>A	rs193303018
m.4284G>A	rs121434468

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