List of variants in gene TMEM67 reported as likely benign for not specified

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_153704.6(TMEM67):c.1066-3C>T	rs3097427	0.65135
NM_153704.6(TMEM67):c.1810A>G (p.Ile604Val)	rs3134031	0.64845
NM_153704.6(TMEM67):c.406+1361C>T	rs73324992	0.04251
NM_153704.6(TMEM67):c.2892A>C (p.Thr964=)	rs16916221	0.04084
NM_153704.6(TMEM67):c.2908-43C>T	rs56307046	0.01977
NM_153704.6(TMEM67):c.870-29A>G	rs116802062	0.01936
NM_153704.6(TMEM67):c.506+48G>A	rs73694924	0.01745
NM_153704.6(TMEM67):c.1288+46C>T	rs73694952	0.01390
NM_153704.6(TMEM67):c.781G>A (p.Asp261Asn)	rs35793208	0.01141
NM_153704.6(TMEM67):c.1774-45A>C	rs73694960	0.00769
NM_153704.6(TMEM67):c.506+18G>T	rs116705535	0.00585
NM_153704.6(TMEM67):c.2161C>T (p.Pro721Ser)	rs116445698	0.00278
NM_153704.6(TMEM67):c.1309C>G (p.Leu437Val)	rs35765535	0.00213
NM_153704.6(TMEM67):c.1078A>G (p.Thr360Ala)	rs140191346	0.00188
NM_153704.6(TMEM67):c.186T>C (p.Cys62=)	rs115660279	0.00145
NM_153704.6(TMEM67):c.2241G>A (p.Gln747=)	rs115563233	0.00128
NM_153704.6(TMEM67):c.869+9A>G	rs372597584	0.00014
NM_153704.6(TMEM67):c.120T>C (p.Ser40=)	rs767999682	0.00012
NM_153704.6(TMEM67):c.717A>G (p.Val239=)	rs111991507	0.00006
NM_153704.6(TMEM67):c.261C>T (p.Ile87=)	rs190249177	0.00004
NM_153704.6(TMEM67):c.2448G>A (p.Leu816=)	rs886038738	0.00003
NM_153704.6(TMEM67):c.652-16A>G	rs569346767	0.00003
NM_153704.6(TMEM67):c.978+13A>G	rs760659884	0.00003
NM_001142301.1(TMEM67):c.-207G>A	rs758890132	0.00001
NM_153704.6(TMEM67):c.-4T>G	rs80108685	0.00001
NM_153704.6(TMEM67):c.2199T>C (p.Tyr733=)	rs774835190	0.00001
NM_001142301.1(TMEM67):c.-207del	rs145334032
NM_001142301.1(TMEM67):c.2522-6del	rs747342409
NM_153704.6(TMEM67):c.1288+15C>T	rs1057523004
NM_153704.6(TMEM67):c.1351C>A (p.Arg451=)	rs116647652
NM_153704.6(TMEM67):c.2010A>G (p.Thr670=)	rs137989705
NM_153704.6(TMEM67):c.313-13dup	rs367575555
NM_153704.6(TMEM67):c.506+18G>A	rs116705535

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