C4084709[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 454185	NM_000245.4(MET):c.13G>A (p.Ala5Thr)	MET (A5T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
Select item 819874	NM_000245.4(MET):c.16G>T (p.Val6Leu)	MET (V6L)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 485749	NM_000245.4(MET):c.22G>A (p.Ala8Thr)	MET (A8T)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GConflicting classifications of pathogenicity
Select item 1735057	NM_000245.4(MET):c.37G>T (p.Val13Leu)	MET (V13L)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +2 more	GUncertain significance
Select item 1736014	NM_000245.4(MET):c.38T>C (p.Val13Ala)	MET (V13A)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +2 more	GUncertain significance
Select item 188112	NM_000245.4(MET):c.40C>T (p.Leu14Phe)	MET (L14F)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 1692567	NM_000245.4(MET):c.62G>A (p.Arg21Lys)	MET (R21K)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GConflicting classifications of pathogenicity
Select item 135974	NM_000245.4(MET):c.65G>T (p.Ser22Ile)	MET (S22I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 1780017	NM_000245.4(MET):c.105G>T (p.Met35Ile)	MET (M35I)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 485736	NM_000245.4(MET):c.105G>C (p.Met35Ile)	MET (M35I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 584704	NM_000245.4(MET):c.135C>G (p.Asn45Lys)	MET (N45K)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +2 more	GUncertain significance
Select item 454188	NM_000245.4(MET):c.142G>A (p.Ala48Thr)	MET (A48T)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GConflicting classifications of pathogenicity
Select item 411909	NM_000245.4(MET):c.143C>G (p.Ala48Gly)	MET (A48G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 819297	NM_000245.4(MET):c.146A>C (p.Glu49Ala)	MET (E49A)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GConflicting classifications of pathogenicity
Select item 184359	NM_000245.4(MET):c.146A>G (p.Glu49Gly)	MET (E49G)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GConflicting classifications of pathogenicity
Select item 864672	NM_000245.4(MET):c.181C>G (p.His61Asp)	MET (H61D)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 1781295	NM_000245.4(MET):c.184A>G (p.Ile62Val)	MET (I62V)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 2676522	NM_000245.4(MET):c.191T>C (p.Leu64Pro)	MET (L64P)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 3241923	NM_000245.4(MET):c.194G>T (p.Gly65Val)	MET (G65V)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 1784380	NM_000245.4(MET):c.200C>A (p.Thr67Asn)	MET (T67N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 584705	NM_000245.4(MET):c.215T>C (p.Val72Ala)	MET (V72A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 1447271	NM_000245.4(MET):c.229G>A (p.Asp77Asn)	MET (D77N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 947148	NM_000245.4(MET):c.230A>C (p.Asp77Ala)	MET (D77A)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +2 more	GUncertain significance
Select item 571424	NM_000245.4(MET):c.278C>G (p.Pro93Arg)	MET (P93R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 581576	NM_000245.4(MET):c.280G>C (p.Asp94His)	MET (D94H)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 93571	NM_000245.4(MET):c.289C>G (p.Pro97Ala)	MET (P97A)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GConflicting classifications of pathogenicity
Select item 485765	NM_000245.4(MET):c.298G>C (p.Asp100His)	MET (D100H)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +2 more	GUncertain significance
Select item 454240	NM_000245.4(MET):c.341A>T (p.Asp114Val)	MET (D114V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 1497651	NM_000245.4(MET):c.348C>G (p.Ile116Met)	MET (I116M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 454242	NM_000245.4(MET):c.356C>T (p.Ala119Val)	MET (A119V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GUncertain significance
Select item 1393298	NM_000245.4(MET):c.401G>A (p.Gly134Asp)	MET (G134D)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 3241924	NM_000245.4(MET):c.539T>A (p.Leu180Gln)	MET (L180Q)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 853501	NM_000245.4(MET):c.541G>A (p.Gly181Arg)	MET (G181R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 41628	NM_000245.4(MET):c.607T>A (p.Ser203Thr)	MET (S203T)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 2676518	NM_000245.4(MET):c.611C>T (p.Ser204Phe)	MET (S204F)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 186588	NM_000245.4(MET):c.640A>G (p.Ile214Val)	MET (I214V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 485746	NM_000245.4(MET):c.654G>T (p.Arg218Ser)	MET (R218S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GConflicting classifications of pathogenicity
Select item 3241917	NM_000245.4(MET):c.683T>C (p.Phe228Ser)	MET (F228S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 135975	NM_000245.4(MET):c.689C>T (p.Thr230Met)	MET (T230M)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 411884	NM_000245.4(MET):c.704T>C (p.Ile235Thr)	MET (I235T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GUncertain significance
Select item 826881	NM_000245.4(MET):c.716C>T (p.Pro239Leu)	MET (P239L)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GUncertain significance
Select item 826917	NM_000245.4(MET):c.721T>C (p.Phe241Leu)	MET (F241L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 485741	NM_000245.4(MET):c.743A>T (p.Lys248Met)	MET (K248M)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 568449	NM_000245.4(MET):c.762A>C (p.Glu254Asp)	MET (E254D)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 2676520	NM_000245.4(MET):c.768C>A (p.Asn256Lys)	MET (N256K)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 485747	NM_000245.4(MET):c.788C>T (p.Thr263Met)	MET (T263M)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GUncertain significance
Select item 411894	NM_000245.4(MET):c.799G>A (p.Glu267Lys)	MET (E267K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GUncertain significance
Select item 2676524	NM_000245.4(MET):c.803C>G (p.Thr268Ser)	MET (T268S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 2676521	NM_000245.4(MET):c.803C>A (p.Thr268Asn)	MET (T268N)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 411915	NM_000245.4(MET):c.808G>C (p.Asp270His)	MET (D270H)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 485734	NM_000245.4(MET):c.818C>A (p.Thr273Asn)	MET (T273N)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 827518	NM_000245.4(MET):c.821T>C (p.Phe274Ser)	MET (F274S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GConflicting classifications of pathogenicity
Select item 2676530	NM_000245.4(MET):c.839G>C (p.Arg280Thr)	MET (R280T)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +2 more	GUncertain significance
Select item 485748	NM_000245.4(MET):c.840G>T (p.Arg280Ser)	MET (R280S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GUncertain significance
Select item 167292	NM_000245.4(MET):c.901A>G (p.Thr301Ala)	MET (T301A)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 844464	NM_000245.4(MET):c.916A>C (p.Lys306Gln)	MET (K306Q)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 584710	NM_000245.4(MET):c.925A>C (p.Thr309Pro)	MET (T309P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 580449	NM_000245.4(MET):c.949C>A (p.Leu317Ile)	MET (L317I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 3241925	NM_000245.4(MET):c.982C>A (p.Gln328Lys)	MET (Q328K)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97	GUncertain significance
Select item 818256	NM_000245.4(MET):c.1008C>G (p.Ser336Arg)	MET (S336R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 41608	NM_000245.4(MET):c.1019A>G (p.Asp340Gly)	MET (D340G)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 132694	NM_000245.4(MET):c.1039G>A (p.Ala347Thr)	MET (A347T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 822043	NM_000245.4(MET):c.1046G>A (p.Ser349Asn)	MET (S349N)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 1448958	NM_000245.4(MET):c.1056T>G (p.Asp352Glu)	MET (D352E)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 3241916	NM_000245.4(MET):c.1063G>C (p.Glu355Gln)	MET (E355Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 219769	NM_000245.4(MET):c.1063G>A (p.Glu355Lys)	MET (E355K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 185606	NM_000245.4(MET):c.1081G>T (p.Ala361Ser)	MET (A361S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GConflicting classifications of pathogenicity
Select item 962356	NM_000245.4(MET):c.1090G>A (p.Ala364Thr)	MET (A364T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 576350	NM_000245.4(MET):c.1114G>A (p.Asp372Asn)	MET (D372N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 188364	NM_000245.4(MET):c.1132G>A (p.Val378Ile)	MET (V378I)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GConflicting classifications of pathogenicity
Select item 454178	NM_000245.4(MET):c.1136A>G (p.Asn379Ser)	MET (N379S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 358684	NM_000245.4(MET):c.1174C>A (p.Pro392Thr)	MET (P392T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GUncertain significance
Select item 524872	NM_000245.4(MET):c.1234C>T (p.Arg412Cys)	MET (R412C)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1471423	NM_000245.4(MET):c.1250G>A (p.Arg417Gln)	MET (R417Q)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 1764569	NM_000245.4(MET):c.1268C>A (p.Ala423Asp)	MET (A423D)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 135958	NM_000245.4(MET):c.1312C>G (p.Leu438Val)	MET (L438V +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +1 more	GUncertain significance
Select item 1437460	NM_000245.4(MET):c.1330A>G (p.Thr444Ala)	MET (T14A +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GUncertain significance
Select item 1429037	NM_000245.4(MET):c.1347C>A (p.Asp449Glu)	MET (D19E +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +1 more	GUncertain significance
Select item 1038186	NM_000245.4(MET):c.1363C>A (p.Leu455Ile)	MET (L25I +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 2710228	NM_000245.4(MET):c.1388T>C (p.Met463Thr)	MET (M33T +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 581580	NM_000245.4(MET):c.1406G>A (p.Arg469Gln)	MET (R469Q +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 640531	NM_000245.4(MET):c.1408T>A (p.Ser470Thr)	MET (S40T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 1462089	NM_000245.4(MET):c.1421C>A (p.Thr474Asn)	MET (T474N +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GUncertain significance
Select item 2676517	NM_000245.4(MET):c.1427A>T (p.His476Leu)	MET (H46L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 660337	NM_000245.4(MET):c.1430T>A (p.Val477Glu)	MET (V477E +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 848962	NM_000245.4(MET):c.1450C>T (p.His484Tyr)	MET (H484Y +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GConflicting classifications of pathogenicity
Select item 216499	NM_000245.4(MET):c.1451A>G (p.His484Arg)	MET (H484R +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 819273	NM_000245.4(MET):c.1459T>A (p.Ser487Thr)	MET (S57T +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 216500	NM_000245.4(MET):c.1472T>C (p.Ile491Thr)	MET (I491T +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 524856	NM_000245.4(MET):c.1477G>C (p.Glu493Gln)	MET (E493Q +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GUncertain significance
Select item 246625	NM_000245.4(MET):c.1484C>G (p.Thr495Arg)	MET (T495R +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 135961	NM_000245.4(MET):c.1510G>T (p.Val504Phe)	MET (V504F +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +3 more	GUncertain significance
Select item 819479	NM_000245.4(MET):c.1532C>T (p.Thr511Met)	MET (T81M +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 945122	NM_000245.4(MET):c.1568T>C (p.Phe523Ser)	MET (F93S +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GUncertain significance
Select item 1015665	NM_000245.4(MET):c.1597C>A (p.Pro533Thr)	MET (P103T +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +1 more	GUncertain significance
Select item 1776377	NM_000245.4(MET):c.1610A>G (p.Gln537Arg)	MET (Q107R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 819701	NM_000245.4(MET):c.1627G>A (p.Asp543Asn)	MET (D113N +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 642174	NM_000245.4(MET):c.1636G>A (p.Val546Met)	MET (V546M +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +2 more	GConflicting classifications of pathogenicity
Select item 184358	NM_000245.4(MET):c.1669A>G (p.Thr557Ala)	MET (T557A +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1 +7 more	GConflicting classifications of pathogenicity
Select item 134654	NM_000245.4(MET):c.1771C>T (p.Arg591Trp)	MET (R591W +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GConflicting classifications of pathogenicity

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