List of variants in gene MT-TL2 studied for MELAS syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.12273A>G	rs1603223644
NC_012920.1(MT-CYB):m.12276G>A	rs1603223645
NC_012920.1(MT-CYB):m.12278T>C	rs1603223646
NC_012920.1(MT-CYB):m.12279A>G	rs1603223647
NC_012920.1(MT-CYB):m.12279A>T	rs1603223647
NC_012920.1(MT-CYB):m.12280A>G	rs1603223649
NC_012920.1(MT-CYB):m.12281C>T	rs1603223651
NC_012920.1(MT-CYB):m.12285T>C	rs386419957
NC_012920.1(MT-CYB):m.12291T>C	rs1603223653
NC_012920.1(MT-CYB):m.12293G>A	rs1603223654
NC_012920.1(MT-CYB):m.12295T>C	rs1603223656
NC_012920.1(MT-CYB):m.12302C>A	rs1603223658
NC_012920.1(MT-CYB):m.12302C>T	rs1603223658
NC_012920.1(MT-CYB):m.12308A>G	rs2853498
NC_012920.1(MT-CYB):m.12310dup	rs1603223659
NC_012920.1(MT-CYB):m.12311T>C	rs201754056
NC_012920.1(MT-CYB):m.12318G>A	rs1603223664
NC_012920.1(MT-CYB):m.12335T>C	rs1603223668
NC_012920.1(MT-TL2):m.12299A>C
m.12297T>C	rs121434464
m.12315G>A	rs121434462

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