"PreventionGenetics, part of Exact Sciences"[submitter] AND "MTMR14"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 703240	NM_001077525.3(MTMR14):c.66G>A (p.Gln22=)	MTMR14	Single nucleotide variant (synonymous variant)	MTMR14-related disorder +1 more	GBenign
Select item 702177	NM_001077525.3(MTMR14):c.519T>A (p.Asp173Glu)	MTMR14 (D173E)	Single nucleotide variant (missense variant)	MTMR14-related disorder +1 more	GBenign/Likely benign
Select item 2059268	NM_001077525.3(MTMR14):c.678-10T>C	MTMR14	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 282725	NM_001077525.3(MTMR14):c.780T>A (p.Asp260Glu)	MTMR14 (D260E)	Single nucleotide variant (missense variant)	MTMR14-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 194117	NM_001077525.3(MTMR14):c.1067C>T (p.Thr356Met)	MTMR14 (T356M)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 2720712	NM_001077525.3(MTMR14):c.1416G>A (p.Ala472=)	MTMR14	Single nucleotide variant (synonymous variant +1 more)	MTMR14-related disorder +1 more	GLikely benign

ClinVar