C1336839[trait identifier] AND "Labcorp Genetics (formerly Invitae), L - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 801437	NM_004958.4(MTOR):c.889G>A (p.Asp297Asn)	MTOR (D297N)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 36768	NM_003000.3(SDHB):c.32G>A (p.Arg11His)	SDHB (R11H)	Single nucleotide variant (missense variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 90512	NM_000251.3(MSH2):c.1045C>G (p.Pro349Ala)	MSH2 (P349A +1 more)	Single nucleotide variant (missense variant)	Lynch syndrome 1 +8 more	GConflicting classifications of pathogenicity
Select item 2215	NM_000551.4(VHL):c.548C>A (p.Ser183Ter)	LOC107303340, VHL (S183* +1 more)	Single nucleotide variant (nonsense +1 more)	Chuvash polycythemia +2 more	GPathogenic
Select item 583929	NC_000007.13:g.(?_116339129)_(116340348_?)dup	MET	Duplication	Papillary renal cell carcinoma type 1	GUncertain significance
Select item 583430	NC_000007.13:g.(?_116339129)_(117144427_?)dup	LOC116186911, LOC123956215 +45 more	Duplication	Papillary renal cell carcinoma type 1	GUncertain significance
Select item 215784	NM_000245.4(MET):c.-7T>C	MET	Single nucleotide variant (5 prime UTR variant +1 more)	Papillary renal cell carcinoma type 1	GLikely benign
Select item 220130	NM_001127500.2(MET):c.(?_-1)_1200+?dup	MET	Duplication	Papillary renal cell carcinoma type 1	GUncertain significance
Select item 358682	NM_000245.4(MET):c.12C>T (p.Pro4=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GLikely benign
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 219710	NM_000245.4(MET):c.36C>T (p.Leu12=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1 +2 more	GBenign/Likely benign
Select item 757215	NM_000245.4(MET):c.51C>T (p.Thr17=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1	GLikely benign
Select item 134649	NM_000245.4(MET):c.71G>A (p.Gly24Glu)	MET (G24E)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 41610	NM_000245.4(MET):c.110T>C (p.Val37Ala)	MET (V37A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer +4 more	GBenign/Likely benign
Select item 454188	NM_000245.4(MET):c.142G>A (p.Ala48Thr)	MET (A48T)	Single nucleotide variant (missense variant +1 more)	not provided +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 93567	NM_000245.4(MET):c.144G>A (p.Ala48=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
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 584706	NM_000245.4(MET):c.236A>G (p.Gln79Arg)	MET (Q79R)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +1 more	GUncertain significance
Select item 799234	NM_000245.4(MET):c.252C>T (p.Tyr84=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 524894	NM_000245.4(MET):c.306C>G (p.Ser102Arg)	MET (S102R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
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 246642	NM_000245.4(MET):c.362T>C (p.Val121Ala)	MET (V121A)	Single nucleotide variant (missense variant +1 more)	Arthrogryposis, distal, IIa 11 +6 more	GUncertain significance
Select item 824062	NM_000245.4(MET):c.367G>A (p.Asp123Asn)	MET (D123N)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 93573	NM_000245.4(MET):c.390C>T (p.Leu130=)	MET	Single nucleotide variant (synonymous variant +1 more)	not provided +4 more	GBenign
Select item 142059	NM_000245.4(MET):c.406G>A (p.Val136Ile)	MET (V136I)	Single nucleotide variant (missense variant +1 more)	Breast carcinoma +8 more	GConflicting classifications of pathogenicity
Select item 454251	NM_000245.4(MET):c.425A>G (p.Gln142Arg)	MET (Q142R)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +2 more	GUncertain significance
Select item 524854	NM_000245.4(MET):c.428G>A (p.Arg143Gln)	MET (R143Q)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GUncertain significance
Select item 824911	NM_000245.4(MET):c.446A>G (p.Asn149Ser)	MET (N149S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 more	GUncertain significance
Select item 135971	NM_000245.4(MET):c.467C>T (p.Ser156Leu)	MET (S156L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 41627	NM_000245.4(MET):c.504G>T (p.Glu168Asp)	MET (E168D)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 93578	NM_000245.4(MET):c.534C>T (p.Ser178=)	MET	Single nucleotide variant (synonymous variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +5 more	GBenign
Select item 584708	NM_000245.4(MET):c.569A>G (p.Asp190Gly)	MET (D190G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 702358	NM_000245.4(MET):c.600C>G (p.Thr200=)	MET	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 216513	NM_000245.4(MET):c.632T>G (p.Leu211Trp)	MET (L211W)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 1753220	NM_000245.4(MET):c.638C>T (p.Ser213Leu)	MET (S213L)	Single nucleotide variant (missense variant +1 more)	Hepatocellular carcinoma +7 more	GUncertain significance
Select item 135973	NM_000245.4(MET):c.639G>A (p.Ser213=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1 +2 more	GLikely benign
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 454255	NM_000245.4(MET):c.690G>A (p.Thr230=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +2 more	GBenign/Likely benign
Select item 576936	NM_000245.4(MET):c.709G>A (p.Val237Ile)	MET (V237I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 more	GUncertain significance
Select item 584709	NM_000245.4(MET):c.728A>G (p.Asp243Gly)	MET (D243G)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +1 more	GUncertain significance
Select item 568449	NM_000245.4(MET):c.762A>C (p.Glu254Asp)	MET (E254D)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +6 more	GConflicting classifications of pathogenicity
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)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GUncertain significance
Select item 647594	NM_000245.4(MET):c.800A>G (p.Glu267Gly)	MET (E267G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 480824	NM_000245.4(MET):c.803C>T (p.Thr268Ile)	MET (T268I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 1762344	NM_000245.4(MET):c.818C>T (p.Thr273Ile)	MET (T273I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GUncertain significance
Select item 485734	NM_000245.4(MET):c.818C>A (p.Thr273Asn)	MET (T273N)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +6 more	GConflicting classifications of pathogenicity
Select item 524884	NM_000245.4(MET):c.850A>G (p.Ile284Val)	MET (I284V)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +7 more	GConflicting classifications of pathogenicity
Select item 584710	NM_000245.4(MET):c.925A>C (p.Thr309Pro)	MET (T309P)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +3 more	GConflicting classifications of pathogenicity
Select item 215795	NM_000245.4(MET):c.939G>A (p.Val313=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1 +3 more	GLikely benign
Select item 41629	NM_000245.4(MET):c.948A>G (p.Ile316Met)	MET (I316M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +7 more	GBenign/Likely benign
Select item 135978	NM_000245.4(MET):c.959C>T (p.Ala320Val)	MET (A320V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 135979	NM_000245.4(MET):c.960G>A (p.Ala320=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +2 more	GBenign/Likely benign
Select item 41630	NM_000245.4(MET):c.967A>G (p.Ser323Gly)	MET (S323G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 358683	NM_000245.4(MET):c.1011G>A (p.Leu337=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
Select item 132694	NM_000245.4(MET):c.1039G>A (p.Ala347Thr)	MET (A347T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 93564	NM_000245.4(MET):c.1076G>A (p.Arg359Gln)	MET (R359Q)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 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)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 93565	NM_000245.4(MET):c.1085T>C (p.Met362Thr)	MET (M362T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 480850	NM_000245.4(MET):c.1099A>G (p.Ile367Val)	MET (I367V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 41611	NM_000245.4(MET):c.1124A>G (p.Asn375Ser)	MET (N375S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 485743	NM_000245.4(MET):c.1125C>G (p.Asn375Lys)	MET (N375K)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 93566	NM_000245.4(MET):c.1131C>T (p.Ile377=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 188364	NM_000245.4(MET):c.1132G>A (p.Val378Ile)	MET (V378I)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 524881	NM_000245.4(MET):c.1157T>G (p.Leu386Arg)	MET (L386R)	Single nucleotide variant (missense variant +1 more)	Osteofibrous dysplasia +6 more	GUncertain significance
Select item 134648	NM_000245.4(MET):c.1171G>A (p.Gly391Arg)	MET (G391R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GUncertain significance
Select item 358684	NM_000245.4(MET):c.1174C>A (p.Pro392Thr)	MET (P392T)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GConflicting classifications of pathogenicity
Select item 135957	NM_000245.4(MET):c.1191C>T (p.Cys397=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1 +3 more	GBenign/Likely benign
Select item 454180	NM_000245.4(MET):c.1238G>A (p.Arg413His)	MET (R413H)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 184639	NM_000245.4(MET):c.1263C>T (p.Thr421=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +3 more	GBenign/Likely benign
Select item 246622	NM_000245.4(MET):c.1278C>T (p.Arg426=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +4 more	GLikely benign
Select item 411885	NM_000245.4(MET):c.1285T>A (p.Leu429Ile)	MET (L429I)	Single nucleotide variant (missense variant +1 more)	not specified +7 more	GUncertain significance
Select item 524876	NM_000245.4(MET):c.1306G>A (p.Glu436Lys)	MET (E436K +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
Select item 358685	NM_000245.4(MET):c.1320A>G (p.Thr440=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
Select item 252899	NM_000245.4(MET):c.1336A>G (p.Ile446Val)	MET (I446V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 135959	NM_000245.4(MET):c.1361A>T (p.Asn454Ile)	MET (N454I +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1	GUncertain significance
Select item 135960	NM_000245.4(MET):c.1412G>A (p.Gly471Glu)	MET (G471E +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 665399	NM_000245.4(MET):c.1414C>T (p.Pro472Ser)	MET (P472S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity
Select item 216498	NM_000245.4(MET):c.1444G>A (p.Asp482Asn)	MET (D482N +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +6 more	GUncertain significance
Select item 848962	NM_000245.4(MET):c.1450C>T (p.His484Tyr)	MET (H484Y +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1 +6 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 524856	NM_000245.4(MET):c.1477G>C (p.Glu493Gln)	MET (E493Q +1 more)	Single nucleotide variant (missense variant)	not provided +7 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 454189	NM_000245.4(MET):c.1489A>G (p.Asn497Asp)	MET (N497D +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +3 more	GUncertain significance
Select item 584711	NM_000245.4(MET):c.1496A>G (p.Asn499Ser)	MET (N499S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1444928	NM_000245.4(MET):c.1507C>G (p.Leu503Val)	MET (L73V +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1 +1 more	GUncertain significance
Select item 135961	NM_000245.4(MET):c.1510G>T (p.Val504Phe)	MET (V504F +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +7 more	GUncertain significance
Select item 252900	NM_001127500.2(MET):c.1528-?_*2262dup4962	LOC126860158, MET +2 more	Duplication	Papillary renal cell carcinoma type 1	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 584713	NM_000245.4(MET):c.1640G>A (p.Arg547Gln)	MET (R547Q +1 more)	Single nucleotide variant (missense variant)	not provided +8 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)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 358686	NM_000245.4(MET):c.1693A>G (p.Ile565Val)	MET (I565V +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
Select item 643144	NC_000007.13:g.(?_116395399)_(116395579_?)dup	MET	Duplication	Renal cell carcinoma +1 more	GUncertain significance
Select item 188358	NM_000245.4(MET):c.1715G>A (p.Ser572Asn)	MET (S572N +1 more)	Single nucleotide variant (missense variant)	not specified +3 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)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 579079	NM_000245.4(MET):c.1772G>A (p.Arg591Gln)	MET (R591Q +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +3 more	GUncertain significance
Select item 246627	NM_000245.4(MET):c.1853C>T (p.Thr618Met)	MET (T618M +1 more)	Single nucleotide variant (missense variant)	Arthrogryposis, distal, IIa 11 +7 more	GConflicting classifications of pathogenicity
Select item 524880	NM_000245.4(MET):c.1862C>T (p.Thr621Ile)	MET (T621I +1 more)	Single nucleotide variant (missense variant)	Osteofibrous dysplasia +7 more	GConflicting classifications of pathogenicity
Select item 358687	NM_000245.4(MET):c.1863-5dup	MET	Duplication (intron variant)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity

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