ClinVar Miner

List of variants in gene MMP14 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 103
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HGVS dbSNP gnomAD frequency
NM_004995.4(MMP14):c.1635C>T (p.Pro545=) rs17881739 0.00289
NM_004995.4(MMP14):c.109G>C (p.Ala37Pro) rs139288377 0.00167
NM_004995.4(MMP14):c.141C>T (p.Pro47=) rs35461486 0.00036
NM_004995.4(MMP14):c.109-14C>T rs367583211 0.00019
NM_004995.4(MMP14):c.1223G>A (p.Arg408Gln) rs753905711 0.00018
NM_004995.4(MMP14):c.1014G>A (p.Glu338=) rs147241325 0.00008
NM_004995.4(MMP14):c.1179G>A (p.Ala393=) rs200424263 0.00008
NM_004995.4(MMP14):c.299G>C (p.Gly100Ala) rs780457340 0.00008
NM_004995.4(MMP14):c.588C>T (p.Gly196=) rs368784954 0.00006
NM_004995.4(MMP14):c.960C>T (p.Asp320=) rs371131343 0.00005
NM_004995.4(MMP14):c.1511A>G (p.Asp504Gly) rs201413207 0.00004
NM_004995.4(MMP14):c.1623C>T (p.Ala541=) rs774346150 0.00004
NM_004995.4(MMP14):c.257+14C>T rs546238476 0.00004
NM_004995.4(MMP14):c.195C>T (p.Ile65=) rs372924469 0.00003
NM_004995.4(MMP14):c.1074C>T (p.Gly358=) rs1014914604 0.00002
NM_004995.4(MMP14):c.1434C>T (p.Tyr478=) rs148273315 0.00002
NM_004995.4(MMP14):c.381-5C>T rs371963061 0.00002
NM_004995.4(MMP14):c.688+19G>C rs1237607805 0.00002
NM_004995.4(MMP14):c.850+10C>A rs779472403 0.00002
NM_004995.4(MMP14):c.1151-4C>A rs753941886 0.00001
NM_004995.4(MMP14):c.1302-18T>G rs753747016 0.00001
NM_004995.4(MMP14):c.303T>A (p.Ala101=) rs147180062 0.00001
NM_004995.4(MMP14):c.546C>T (p.Ala182=) rs1473138788 0.00001
NM_004995.4(MMP14):c.733C>T (p.Leu245=) rs1355370825 0.00001
NM_004995.4(MMP14):c.1011+17T>C
NM_004995.4(MMP14):c.1017C>T (p.Arg339=)
NM_004995.4(MMP14):c.105C>A (p.Pro35=)
NM_004995.4(MMP14):c.108+16G>C
NM_004995.4(MMP14):c.108+20C>A rs2138732803
NM_004995.4(MMP14):c.109-18A>G
NM_004995.4(MMP14):c.1150+11dup
NM_004995.4(MMP14):c.1150+7A>T
NM_004995.4(MMP14):c.1236C>T (p.Thr412=)
NM_004995.4(MMP14):c.123A>G (p.Gln41=)
NM_004995.4(MMP14):c.1242G>A (p.Lys414=)
NM_004995.4(MMP14):c.1281C>T (p.Thr427=)
NM_004995.4(MMP14):c.1302-19T>G
NM_004995.4(MMP14):c.1302-6C>T
NM_004995.4(MMP14):c.1308C>T (p.Tyr436=)
NM_004995.4(MMP14):c.1317C>T (p.Asn439=)
NM_004995.4(MMP14):c.1417+8G>C
NM_004995.4(MMP14):c.1428C>T (p.Tyr476=)
NM_004995.4(MMP14):c.1443C>T (p.Asn481=)
NM_004995.4(MMP14):c.1539G>T (p.Arg513=)
NM_004995.4(MMP14):c.153T>C (p.Arg51=)
NM_004995.4(MMP14):c.1542G>A (p.Pro514=)
NM_004995.4(MMP14):c.1557G>A (p.Glu519=)
NM_004995.4(MMP14):c.1569G>A (p.Glu523=)
NM_004995.4(MMP14):c.1599C>T (p.Gly533=)
NM_004995.4(MMP14):c.1614C>T (p.Ser538=)
NM_004995.4(MMP14):c.1617G>A (p.Ala539=)
NM_004995.4(MMP14):c.162A>G (p.Thr54=)
NM_004995.4(MMP14):c.1635C>G (p.Pro545=)
NM_004995.4(MMP14):c.1653G>T (p.Leu551=)
NM_004995.4(MMP14):c.165G>A (p.Gln55=)
NM_004995.4(MMP14):c.1662G>A (p.Ala554=)
NM_004995.4(MMP14):c.1716C>T (p.Leu572=)
NM_004995.4(MMP14):c.171A>G (p.Ser57=) rs1595014148
NM_004995.4(MMP14):c.1731C>A (p.Ser577=)
NM_004995.4(MMP14):c.1740C>T (p.Asp580=)
NM_004995.4(MMP14):c.183C>G (p.Leu61=)
NM_004995.4(MMP14):c.189G>A (p.Ala63=)
NM_004995.4(MMP14):c.216C>T (p.Tyr72=)
NM_004995.4(MMP14):c.257+19C>T
NM_004995.4(MMP14):c.258-11A>T
NM_004995.4(MMP14):c.258-19G>A
NM_004995.4(MMP14):c.258-7A>T
NM_004995.4(MMP14):c.294G>A (p.Lys98=) rs772534496
NM_004995.4(MMP14):c.318T>C (p.Asn106=)
NM_004995.4(MMP14):c.336C>T (p.Tyr112=)
NM_004995.4(MMP14):c.36G>C (p.Leu12=)
NM_004995.4(MMP14):c.380+11C>T
NM_004995.4(MMP14):c.380+11dup
NM_004995.4(MMP14):c.381-16C>T
NM_004995.4(MMP14):c.408C>T (p.Gly136=)
NM_004995.4(MMP14):c.441G>A (p.Ala147=)
NM_004995.4(MMP14):c.480C>T (p.Arg160=)
NM_004995.4(MMP14):c.561C>G (p.Gly187=)
NM_004995.4(MMP14):c.570G>A (p.Thr190=)
NM_004995.4(MMP14):c.594C>T (p.Phe198=)
NM_004995.4(MMP14):c.627T>A (p.Ile209=)
NM_004995.4(MMP14):c.688+11_688+19del rs776053716
NM_004995.4(MMP14):c.688+15C>G
NM_004995.4(MMP14):c.689-7C>T
NM_004995.4(MMP14):c.699C>T (p.Ile233=)
NM_004995.4(MMP14):c.717C>T (p.His239=)
NM_004995.4(MMP14):c.721C>T (p.Leu241=)
NM_004995.4(MMP14):c.756C>T (p.Asp252=)
NM_004995.4(MMP14):c.762G>A (p.Ser254=)
NM_004995.4(MMP14):c.777C>A (p.Pro259=) rs2236302
NM_004995.4(MMP14):c.811C>T (p.Leu271=)
NM_004995.4(MMP14):c.816C>T (p.Pro272=)
NM_004995.4(MMP14):c.81G>C (p.Ser27=)
NM_004995.4(MMP14):c.843A>G (p.Gln281=)
NM_004995.4(MMP14):c.850+13C>T
NM_004995.4(MMP14):c.850+19C>T
NM_004995.4(MMP14):c.850+20G>A
NM_004995.4(MMP14):c.851-16G>A
NM_004995.4(MMP14):c.851-17C>T rs770053777
NM_004995.4(MMP14):c.851-6C>T
NM_004995.4(MMP14):c.858G>A (p.Glu286=)
NM_004995.4(MMP14):c.93C>T (p.Ser31=) rs2138732719
NM_004995.4(MMP14):c.975C>T (p.Thr325=)

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