"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MET"[ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166750	NM_000245.4(MET):c.-207C>G	COMETT, MET	Single nucleotide variant (5 prime UTR variant)	Renal cell carcinoma +1 more	GBenign
Select item 569107	NM_000245.4(MET):c.-12_17del (p.Met1fs)	MET (M1fs)	Deletion (frameshift variant +2 more)	Renal cell carcinoma +1 more	GUncertain significance
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 841732	NM_000245.4(MET):c.7G>A (p.Ala3Thr)	MET (A3T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 2801430	NM_000245.4(MET):c.8C>T (p.Ala3Val)	MET (A3V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1154382	NM_000245.4(MET):c.9C>T (p.Ala3=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 1143886	NM_000245.4(MET):c.12C>G (p.Pro4=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
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 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 1778331	NM_000245.4(MET):c.16G>A (p.Val6Met)	MET (V6M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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 2919100	NM_000245.4(MET):c.17T>G (p.Val6Gly)	MET (V6G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1126235	NM_000245.4(MET):c.21T>G (p.Leu7=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
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 2920571	NM_000245.4(MET):c.24dup (p.Pro9fs)	MET (P9fs)	Duplication (frameshift variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1516929	NM_000245.4(MET):c.25C>T (p.Pro9Ser)	MET (P9S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1478952	NM_000245.4(MET):c.25C>A (p.Pro9Thr)	MET (P9T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1006595	NM_000245.4(MET):c.26C>T (p.Pro9Leu)	MET (P9L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1538697	NM_000245.4(MET):c.27T>G (p.Pro9=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 970706	NM_000245.4(MET):c.29G>A (p.Gly10Asp)	MET (G10D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2855423	NM_000245.4(MET):c.30C>T (p.Gly10=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 640609	NM_000245.4(MET):c.31A>G (p.Ile11Val)	MET (I11V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 1367128	NM_000245.4(MET):c.34C>T (p.Leu12Phe)	MET (L12F)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 641845	NM_000245.4(MET):c.36C>A (p.Leu12=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GConflicting classifications of pathogenicity
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 2907157	NM_000245.4(MET):c.37G>C (p.Val13Leu)	MET (V13L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1735057	NM_000245.4(MET):c.37G>T (p.Val13Leu)	MET (V13L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GUncertain significance
Select item 411901	NM_000245.4(MET):c.37G>A (p.Val13Met)	MET (V13M)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
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)	Renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 1115623	NM_000245.4(MET):c.42C>G (p.Leu14=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 1634616	NM_000245.4(MET):c.43C>T (p.Leu15=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2154734	NM_000245.4(MET):c.47T>G (p.Phe16Cys)	MET (F16C)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 825439	NM_000245.4(MET):c.50C>G (p.Thr17Ser)	MET (T17S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 665396	NM_000245.4(MET):c.50C>T (p.Thr17Ile)	MET (T17I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
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 2787263	NM_000245.4(MET):c.52T>G (p.Leu18Val)	MET (L18V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2154156	NM_000245.4(MET):c.52T>C (p.Leu18=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 794620	NM_000245.4(MET):c.57G>A (p.Val19=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 2736820	NM_000245.4(MET):c.61A>G (p.Arg21Gly)	MET (R21G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1692567	NM_000245.4(MET):c.62G>A (p.Arg21Lys)	MET (R21K)	Single nucleotide variant (missense variant +1 more)	not provided +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 1949562	NM_000245.4(MET):c.66C>G (p.Ser22Arg)	MET (S22R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 826560	NM_000245.4(MET):c.66C>A (p.Ser22Arg)	MET (S22R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 1956254	NM_000245.4(MET):c.69T>C (p.Asn23=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	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 826954	NM_000245.4(MET):c.72G>A (p.Gly24=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1461779	NM_000245.4(MET):c.73G>T (p.Glu25Ter)	MET (E25*)	Single nucleotide variant (nonsense +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1108190	NM_000245.4(MET):c.75G>A (p.Glu25=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 1378972	NM_000245.4(MET):c.76T>C (p.Cys26Arg)	MET (C26R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1442248	NM_000245.4(MET):c.79A>T (p.Lys27Ter)	MET (K27*)	Single nucleotide variant (nonsense +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2119357	NM_000245.4(MET):c.80_81delinsGG (p.Lys27Arg)	MET (K27R)	Indel (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 577544	NM_000245.4(MET):c.80A>G (p.Lys27Arg)	MET (K27R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2766545	NM_000245.4(MET):c.82G>C (p.Glu28Gln)	MET (E28Q)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 581052	NM_000245.4(MET):c.82G>A (p.Glu28Lys)	MET (E28K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2753653	NM_000245.4(MET):c.83A>T (p.Glu28Val)	MET (E28V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1521376	NM_000245.4(MET):c.84G>C (p.Glu28Asp)	MET (E28D)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1364179	NM_000245.4(MET):c.85G>T (p.Ala29Ser)	MET (A29S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1350657	NM_000245.4(MET):c.85G>C (p.Ala29Pro)	MET (A29P)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 822670	NM_000245.4(MET):c.86C>T (p.Ala29Val)	MET (A29V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GBenign/Likely benign
Select item 756549	NM_000245.4(MET):c.87A>G (p.Ala29=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 416925	NM_000245.4(MET):c.88C>T (p.Leu30=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 2108063	NM_000245.4(MET):c.89T>C (p.Leu30Pro)	MET (L30P)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1766491	NM_000245.4(MET):c.92C>T (p.Ala31Val)	MET (A31V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GConflicting classifications of pathogenicity
Select item 705401	NM_000245.4(MET):c.93A>G (p.Ala31=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 1127332	NM_000245.4(MET):c.96G>A (p.Lys32=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 485740	NM_000245.4(MET):c.99C>T (p.Ser33=)	MET	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 936149	NM_000245.4(MET):c.100G>C (p.Glu34Gln)	MET (E34Q)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 411897	NM_000245.4(MET):c.100G>A (p.Glu34Lys)	MET (E34K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 1003572	NM_000245.4(MET):c.102G>C (p.Glu34Asp)	MET (E34D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 134646	NM_000245.4(MET):c.103A>T (p.Met35Leu)	MET (M35L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 2453414	NM_000245.4(MET):c.104T>C (p.Met35Thr)	MET (M35T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1370403	NM_000245.4(MET):c.105G>A (p.Met35Ile)	MET (M35I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	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 1318641	NM_000245.4(MET):c.107A>G (p.Asn36Ser)	MET (N36S)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 1569150	NM_000245.4(MET):c.108T>C (p.Asn36=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 216496	NM_000245.4(MET):c.109G>T (p.Val37Leu)	MET (V37L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
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 216497	NM_000245.4(MET):c.114T>A (p.Asn38Lys)	MET (N38K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GConflicting classifications of pathogenicity
Select item 943035	NM_000245.4(MET):c.116T>A (p.Met39Lys)	MET (M39K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 246619	NM_000245.4(MET):c.116T>C (p.Met39Thr)	MET (M39T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 2090262	NM_000245.4(MET):c.117G>A (p.Met39Ile)	MET (M39I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 818558	NM_000245.4(MET):c.119A>T (p.Lys40Met)	MET (K40M)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1016149	NM_000245.4(MET):c.122A>G (p.Tyr41Cys)	MET (Y41C)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 524867	NM_000245.4(MET):c.128T>C (p.Leu43Pro)	MET (L43P)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 2103484	NM_000245.4(MET):c.129T>C (p.Leu43=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 858401	NM_000245.4(MET):c.130C>T (p.Pro44Ser)	MET (P44S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 524896	NM_000245.4(MET):c.131C>A (p.Pro44His)	MET (P44H)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GUncertain significance
Select item 2746619	NM_000245.4(MET):c.133A>G (p.Asn45Asp)	MET (N45D)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 1443234	NM_000245.4(MET):c.134A>G (p.Asn45Ser)	MET (N45S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2148518	NM_000245.4(MET):c.135C>T (p.Asn45=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 2814023	NM_000245.4(MET):c.139A>T (p.Thr47Ser)	MET (T47S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2878627	NM_000245.4(MET):c.140C>T (p.Thr47Ile)	MET (T47I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +1 more	GConflicting classifications of pathogenicity
Select item 1461574	NM_000245.4(MET):c.140C>A (p.Thr47Asn)	MET (T47N)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 834610	NM_000245.4(MET):c.141C>A (p.Thr47=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 454186	NM_000245.4(MET):c.141C>G (p.Thr47=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +1 more	GLikely benign
Select item 219723	NM_000245.4(MET):c.141C>T (p.Thr47=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign

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