List of variants in gene MET reported as uncertain significance by Mendelics

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.406G>A (p.Val136Ile)	rs199701987	0.00058
NM_000245.4(MET):c.1076G>A (p.Arg359Gln)	rs201274041	0.00022
NM_000245.4(MET):c.1771C>T (p.Arg591Trp)	rs45602940	0.00015
NM_000245.4(MET):c.40C>T (p.Leu14Phe)	rs763344951	0.00015
NM_000245.4(MET):c.803C>T (p.Thr268Ile)	rs757427533	0.00007
NM_000245.4(MET):c.1988C>T (p.Ser663Leu)	rs376459715	0.00005
NM_000245.4(MET):c.4007G>A (p.Arg1336Gln)	rs369312680	0.00005
NM_000245.4(MET):c.2825C>T (p.Ser942Leu)	rs375576430	0.00004
NM_000245.4(MET):c.428G>A (p.Arg143Gln)	rs35469582	0.00004
NM_000245.4(MET):c.3356G>C (p.Gly1119Ala)	rs201037977	0.00003
NM_000245.4(MET):c.4100C>G (p.Ser1367Cys)	rs747239403	0.00003
NM_000245.4(MET):c.1171G>A (p.Gly391Arg)	rs587778443	0.00001
NM_000245.4(MET):c.1238G>A (p.Arg413His)	rs375391602	0.00001
NM_000245.4(MET):c.1444G>A (p.Asp482Asn)	rs863224694	0.00001
NM_000245.4(MET):c.1451A>G (p.His484Arg)	rs781545528	0.00001
NM_000245.4(MET):c.1904A>G (p.Asn635Ser)	rs773826297	0.00001
NM_000245.4(MET):c.2102+7T>C	rs1584941903	0.00001
NM_000245.4(MET):c.215T>C (p.Val72Ala)	rs973796037	0.00001
NM_000245.4(MET):c.2192G>A (p.Arg731Gln)	rs45446492	0.00001
NM_000245.4(MET):c.2716G>A (p.Glu906Lys)	rs778115147	0.00001
NM_000245.4(MET):c.362T>C (p.Val121Ala)	rs879254339	0.00001
NM_000245.4(MET):c.3878C>G (p.Thr1293Ser)	rs779121848	0.00001
NM_000245.4(MET):c.1125C>G (p.Asn375Lys)	rs776693512
NM_000245.4(MET):c.135C>G (p.Asn45Lys)	rs1562883006
NM_000245.4(MET):c.1393-1G>T	rs1584921909
NM_000245.4(MET):c.1496A>G (p.Asn499Ser)	rs1253878709
NM_000245.4(MET):c.1508T>A (p.Leu503Gln)	rs1562908826
NM_000245.4(MET):c.1541C>T (p.Pro514Leu)
NM_000245.4(MET):c.1866G>C (p.Leu622Phe)	rs1562921668
NM_000245.4(MET):c.1933G>A (p.Gly645Arg)	rs763849125
NM_000245.4(MET):c.2255C>A (p.Ser752Tyr)
NM_000245.4(MET):c.236A>G (p.Gln79Arg)	rs1562883214
NM_000245.4(MET):c.2510A>G (p.His837Arg)	rs1041349799
NM_000245.4(MET):c.253A>G (p.Lys85Glu)	rs1791469321
NM_000245.4(MET):c.2568T>G (p.Asn856Lys)	rs118057172
NM_000245.4(MET):c.2672C>G (p.Ala891Gly)	rs1562929174
NM_000245.4(MET):c.2887+5A>T	rs752292538
NM_000245.4(MET):c.2892G>A (p.Leu964=)	rs1584955273
NM_000245.4(MET):c.2995G>C (p.Glu999Gln)	rs1404824650
NM_000245.4(MET):c.3151G>A (p.Val1051Ile)	rs775997318
NM_000245.4(MET):c.3352A>G (p.Ile1118Val)	rs755234697
NM_000245.4(MET):c.3991T>G (p.Ser1331Ala)	rs1562941559
NM_000245.4(MET):c.4041G>T (p.Glu1347Asp)	rs1562941622
NM_000245.4(MET):c.4097C>T (p.Pro1366Leu)	rs778084120
NM_000245.4(MET):c.410A>G (p.Asn137Ser)	rs1584876716
NM_000245.4(MET):c.4140C>A (p.Asp1380Glu)	rs370368651
NM_000245.4(MET):c.569A>G (p.Asp190Gly)	rs1028165414
NM_000245.4(MET):c.728A>G (p.Asp243Gly)	rs1562883992
NM_000245.4(MET):c.925A>C (p.Thr309Pro)	rs35601148

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