ClinVar Miner

Variants with conflicting interpretations "benign" from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine and "likely benign" from any submitter

Minimum review status of the submission from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine: Collection method of the submission from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 16
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HGVS dbSNP
NM_000018.4(ACADVL):c.1182+17C>A rs191276923
NM_000018.4(ACADVL):c.308A>G (p.Lys103Arg) rs140566084
NM_001126131.2(POLG):c.1550G>T (p.Gly517Val) rs61752783
NM_002693.2(POLG):c.150G>A (p.Gln50=) rs766501874
NM_002693.2(POLG):c.1837C>T (p.His613Tyr) rs147407423
NM_002693.2(POLG):c.2028G>A (p.Ala676=) rs373550219
NM_002693.2(POLG):c.2853C>T (p.Tyr951=) rs41546712
NM_002693.2(POLG):c.3274-19G>A rs116925016
NM_002693.2(POLG):c.3405C>T (p.Asp1135=) rs2307445
NM_002693.2(POLG):c.803G>C (p.Gly268Ala) rs61752784
NM_006567.5(FARS2):c.1014C>T (p.Arg338=) rs41302855
NM_006567.5(FARS2):c.462G>T (p.Ala154=) rs150477330
NM_006567.5(FARS2):c.606G>A (p.Lys202=) rs17851782
NM_006567.5(FARS2):c.768A>C (p.Gly256=) rs200003967
NM_006567.5(FARS2):c.819T>A (p.Pro273=) rs201042275
NM_006567.5(FARS2):c.873C>T (p.Cys291=) rs372301183

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