List of variants in gene MTFMT reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 47

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HGVS	dbSNP	gnomAD frequency
NM_139242.4(MTFMT):c.814-143C>T	rs4776660	0.97833
NM_139242.4(MTFMT):c.814-246G>A	rs2414867	0.51095
NM_139242.4(MTFMT):c.814-248G>A	rs55873149	0.50875
NM_139242.4(MTFMT):c.420-254A>G	rs2946660	0.39280
NM_139242.4(MTFMT):c.542+49A>G	rs4776661	0.36497
NM_139242.4(MTFMT):c.542+275A>C	rs35328312	0.34215
NM_139242.4(MTFMT):c.14T>C (p.Val5Ala)	rs2946655	0.07188
NM_139242.4(MTFMT):c.646-182T>C	rs79721848	0.04336
NM_139242.4(MTFMT):c.*293G>C	rs62015300	0.02679
NM_139242.4(MTFMT):c.1065G>A (p.Gln355=)	rs35477493	0.02430
NM_139242.4(MTFMT):c.906G>A (p.Thr302=)	rs34636936	0.01698
NM_139242.4(MTFMT):c.172T>A (p.Phe58Ile)	rs188718836	0.01018
NM_139242.4(MTFMT):c.210-6A>C	rs144496904	0.00947
NM_139242.4(MTFMT):c.796C>T (p.Arg266Cys)	rs35302908	0.00884
NM_139242.4(MTFMT):c.892+17del	rs530492914	0.00424
NM_139242.4(MTFMT):c.667T>A (p.Leu223Met)	rs188461284	0.00375
NM_139242.4(MTFMT):c.186G>C (p.Ala62=)	rs183891284	0.00256
NM_139242.4(MTFMT):c.601G>A (p.Ala201Thr)	rs111388106	0.00185
NM_139242.4(MTFMT):c.847A>G (p.Ile283Val)	rs114097513	0.00185
NM_139242.4(MTFMT):c.396G>A (p.Glu132=)	rs139698971	0.00091
NM_139242.4(MTFMT):c.476T>C (p.Val159Ala)	rs571610853	0.00088
NM_139242.4(MTFMT):c.885C>T (p.Val295=)	rs202082622	0.00058
NM_139242.4(MTFMT):c.1092A>G (p.Gln364=)	rs4586374	0.00050
NM_139242.4(MTFMT):c.645+19C>G	rs201472455	0.00015
NC_000015.10:g.65029827_65029828insATTTATTTATTT	rs764189876
NC_000015.10:g.65029827_65029828insATTTATTTATTTATTT	rs764189876
NC_000015.10:g.65029827_65029828insATTTATTTATTTATTTATTT	rs764189876
NC_000015.10:g.65029828C>A	rs28583784
NC_000015.10:g.65029832ATTT[11]	rs58967026
NC_000015.10:g.65029832ATTT[12]	rs58967026
NC_000015.10:g.65029832ATTT[13]	rs58967026
NC_000015.10:g.65029832ATTT[7]	rs58967026
NM_139242.4(MTFMT):c.*100G>T	rs866953579
NM_139242.4(MTFMT):c.*99dup	rs398027674
NM_139242.4(MTFMT):c.1068A>G (p.Lys356=)
NM_139242.4(MTFMT):c.1129A>C (p.Lys377Gln)	rs34507711
NM_139242.4(MTFMT):c.16C>G (p.Arg6Gly)	rs199599204
NM_139242.4(MTFMT):c.16C>T (p.Arg6Trp)	rs199599204
NM_139242.4(MTFMT):c.646-124del	rs11358848
NM_139242.4(MTFMT):c.646-18_646-17dup	rs372515409
NM_139242.4(MTFMT):c.646-18dup	rs372515409
NM_139242.4(MTFMT):c.646-5del	rs372515409
NM_139242.4(MTFMT):c.722-116A>T	rs12912782
NM_139242.4(MTFMT):c.722-256del	rs35437034
NM_139242.4(MTFMT):c.813+191G>C	rs34348990
NM_139242.4(MTFMT):c.814-204dup	rs796457972
NM_139242.4(MTFMT):c.814-217G>C	rs61660583

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