"PreventionGenetics, part of Exact Sciences"[submitter] AND "MMP14"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1279198	NM_004995.4(MMP14):c.22C>T (p.Pro8Ser)	MMP14 (P8S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1232955	NM_004995.4(MMP14):c.777C>G (p.Pro259=)	MMP14	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1177852	NM_004995.4(MMP14):c.855T>C (p.Gly285=)	MMP14	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 778734	NM_004995.4(MMP14):c.1287C>T (p.Phe429=)	MMP14	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 717373	NM_004995.4(MMP14):c.1292G>A (p.Arg431His)	MMP14 (R431H)	Single nucleotide variant (missense variant)	MMP14-related disorder +1 more	GBenign
Select item 3052224	NM_004995.4(MMP14):c.*9G>A	MMP14	Single nucleotide variant (3 prime UTR variant)	MMP14-related disorder	GBenign

ClinVar