"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "DLC1"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 373548	NM_182643.3(DLC1):c.4582A>T (p.Arg1528Trp)	DLC1 (R1528W +3 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2041358	NM_182643.3(DLC1):c.4537G>A (p.Asp1513Asn)	DLC1 (D1002N +9 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2052332	NM_182643.3(DLC1):c.4525G>A (p.Val1509Ile)	DLC1 (V1033I +9 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2011608	NM_182643.3(DLC1):c.4505A>G (p.His1502Arg)	DLC1 (H1502R +9 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2087420	NM_182643.3(DLC1):c.4488C>T (p.Tyr1496=)	DLC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2172546	NM_182643.3(DLC1):c.4466+10G>C	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2704357	NM_182643.3(DLC1):c.4466+9T>C	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2055308	NM_182643.3(DLC1):c.4466+8C>G	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2074937	NM_182643.3(DLC1):c.4466+4T>A	DLC1	Single nucleotide variant (intron variant)	Colorectal cancer +1 more	GConflicting classifications of pathogenicity
Select item 2783280	NM_182643.3(DLC1):c.4449G>T (p.Met1483Ile)	DLC1 (M1046I +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2170835	NM_182643.3(DLC1):c.4410T>G (p.Ile1470Met)	DLC1 (I1067M +9 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2065100	NM_182643.3(DLC1):c.4360G>A (p.Ala1454Thr)	DLC1 (A934T +9 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2180899	NM_182643.3(DLC1):c.4351C>G (p.His1451Asp)	DLC1 (H975D +9 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GUncertain significance
Select item 2019479	NM_182643.3(DLC1):c.4314C>T (p.Pro1438=)	DLC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2181927	NM_182643.3(DLC1):c.4293A>G (p.Arg1431=)	DLC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 1972290	NM_182643.3(DLC1):c.4293-3C>T	DLC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2050411	NM_182643.3(DLC1):c.4292+7G>A	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1977221	NM_182643.3(DLC1):c.4292+3G>A	DLC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2172547	NM_182643.3(DLC1):c.4282G>A (p.Val1428Ile)	DLC1 (V1428I +9 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1380122	NM_182643.3(DLC1):c.4274G>A (p.Arg1425Gln)	DLC1 (R1425Q +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2195152	NM_182643.3(DLC1):c.4207G>A (p.Glu1403Lys)	DLC1 (E1045K +9 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2765826	NM_182643.3(DLC1):c.4188G>T (p.Leu1396=)	DLC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1974465	NM_182643.3(DLC1):c.4160A>T (p.Lys1387Ile)	DLC1 (K1029I +9 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2187219	NM_182643.3(DLC1):c.4155A>G (p.Leu1385=)	DLC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2107818	NM_182643.3(DLC1):c.4135G>A (p.Glu1379Lys)	DLC1 (E868K +9 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2070239	NM_182643.3(DLC1):c.4080C>T (p.Ser1360=)	DLC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 724888	NM_182643.3(DLC1):c.4062G>A (p.Leu1354=)	DLC1, LOC126860305	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2636814	NM_182643.3(DLC1):c.4046C>G (p.Ser1349Trp)	DLC1, LOC126860305 (S1349W +7 more)	Single nucleotide variant (missense variant +1 more)	DLC1-related disorder +1 more	GUncertain significance
Select item 2039491	NM_182643.3(DLC1):c.4046C>T (p.Ser1349Leu)	DLC1, LOC126860305 (S838L +7 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2758964	NM_182643.3(DLC1):c.4006G>C (p.Val1336Leu)	DLC1, LOC126860305 (V1336L +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2065763	NM_182643.3(DLC1):c.3979G>T (p.Asp1327Tyr)	DLC1, LOC126860305 (D807Y +7 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2130938	NM_182643.3(DLC1):c.3977A>G (p.Gln1326Arg)	DLC1, LOC126860305 (Q1326R +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2764500	NM_182643.3(DLC1):c.3968A>T (p.His1323Leu)	DLC1, LOC126860305 (H803L +7 more)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +1 more	GLikely benign
Select item 2123502	NM_182643.3(DLC1):c.3951C>A (p.Asp1317Glu)	DLC1, LOC126860305 (D797E +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2871280	NM_182643.3(DLC1):c.3947A>G (p.Asp1316Gly)	DLC1, LOC126860305 (D879G +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2911688	NM_182643.3(DLC1):c.3916A>G (p.Thr1306Ala)	DLC1, LOC126860305 (T869A +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2870598	NM_182643.3(DLC1):c.3903G>T (p.Glu1301Asp)	DLC1, LOC126860305 (E909D +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2775906	NM_182643.3(DLC1):c.3881G>A (p.Arg1294His)	DLC1, LOC126860305 (R888H +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2215105	NM_182643.3(DLC1):c.3859C>T (p.Pro1287Ser)	DLC1, LOC126860305 (P1287S +7 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1328014	NM_182643.3(DLC1):c.3856-6G>A	DLC1, LOC126860305	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2880534	NM_182643.3(DLC1):c.3856-8C>T	DLC1, LOC126860305	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2807842	NM_182643.3(DLC1):c.3847C>A (p.Leu1283Ile)	DLC1 (L846I +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2052952	NM_182643.3(DLC1):c.3834C>T (p.Ala1278=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2892527	NM_182643.3(DLC1):c.3821C>A (p.Ala1274Asp)	DLC1 (A1274D +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2420185	NM_182643.3(DLC1):c.3819G>A (p.Leu1273=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2172861	NM_182643.3(DLC1):c.3803C>T (p.Ala1268Val)	DLC1 (A1268V +7 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2866291	NM_182643.3(DLC1):c.3743T>A (p.Val1248Glu)	DLC1 (V842E +7 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2084501	NM_182643.3(DLC1):c.3742G>A (p.Val1248Ile)	DLC1 (V1248I +7 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GUncertain significance
Select item 1600292	NM_182643.3(DLC1):c.3741-10T>C	DLC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1972910	NM_182643.3(DLC1):c.3741-18T>C	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2784302	NM_182643.3(DLC1):c.3741-20C>G	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868646	NM_182643.3(DLC1):c.3740+16G>T	DLC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1971797	NM_182643.3(DLC1):c.3740+12A>G	DLC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1220844	NM_182643.3(DLC1):c.3740+11C>T	DLC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2082393	NM_182643.3(DLC1):c.3737C>T (p.Pro1246Leu)	DLC1 (P726L +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2889332	NM_182643.3(DLC1):c.3690G>A (p.Ala1230=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2363901	NM_182643.3(DLC1):c.3643G>A (p.Val1215Ile)	DLC1 (V812I +7 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2863595	NM_182643.3(DLC1):c.3617A>G (p.Tyr1206Cys)	DLC1 (Y769C +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 737441	NM_182643.3(DLC1):c.3609C>A (p.Thr1203=)	DLC1	Single nucleotide variant (synonymous variant)	Colorectal cancer +1 more	GLikely benign
Select item 2695532	NM_182643.3(DLC1):c.3589A>G (p.Asn1197Asp)	DLC1 (N1197D +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 781766	NM_182643.3(DLC1):c.3551A>T (p.Gln1184Leu)	DLC1 (Q673L +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1282045	NM_182643.3(DLC1):c.3546C>A (p.Arg1182=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 784124	NM_182643.3(DLC1):c.3528T>C (p.Tyr1176=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2169282	NM_182643.3(DLC1):c.3527-3C>T	DLC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1971120	NM_182643.3(DLC1):c.3527-17G>T	DLC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179905	NM_182643.3(DLC1):c.3501G>A (p.Ser1167=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2571309	NM_182643.3(DLC1):c.3489G>A (p.Thr1163=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1974204	NM_182643.3(DLC1):c.3445A>G (p.Met1149Val)	DLC1 (M638V +7 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2119579	NM_182643.3(DLC1):c.3417A>T (p.Glu1139Asp)	DLC1 (E1139D +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2157274	NM_182643.3(DLC1):c.3401A>G (p.Asp1134Gly)	DLC1 (D742G +7 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 2872388	NM_182643.3(DLC1):c.3397A>G (p.Ile1133Val)	DLC1 (I1133V +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2041359	NM_182643.3(DLC1):c.3389A>G (p.Glu1130Gly)	DLC1 (E1130G +7 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2065069	NM_182643.3(DLC1):c.3348G>A (p.Ser1116=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2190978	NM_182643.3(DLC1):c.3328-3_3328-2insCACT	DLC1	Insertion (intron variant)	not provided	GUncertain significance
Select item 2190979	NM_182643.3(DLC1):c.3328-3C>A	DLC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1972505	NM_182643.3(DLC1):c.3327+18G>A	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2865592	NM_182643.3(DLC1):c.3327+17C>T	DLC1	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 736557	NM_182643.3(DLC1):c.3327+8C>T	DLC1	Single nucleotide variant (intron variant)	Colorectal cancer +1 more	GLikely benign
Select item 1998721	NM_182643.3(DLC1):c.3319T>A (p.Leu1107Met)	DLC1 (L1107M +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2260523	NM_182643.3(DLC1):c.3299G>A (p.Arg1100Gln)	DLC1 (R580Q +7 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2066143	NM_182643.3(DLC1):c.3283A>G (p.Ile1095Val)	DLC1 (I575V +7 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2054151	NM_182643.3(DLC1):c.3270G>A (p.Pro1090=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2077456	NM_182643.3(DLC1):c.3267A>G (p.Gln1089=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2873208	NM_182643.3(DLC1):c.3167+18C>A	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2876777	NM_182643.3(DLC1):c.3167+14T>C	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2156581	NM_182643.3(DLC1):c.3164G>C (p.Ser1055Thr)	DLC1 (S652T +7 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2039056	NM_182643.3(DLC1):c.3080A>G (p.Gln1027Arg)	DLC1 (Q1027R +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2865888	NM_182643.3(DLC1):c.3029G>A (p.Arg1010Gln)	DLC1 (R1010Q +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2841958	NM_182643.3(DLC1):c.3009C>G (p.His1003Gln)	DLC1 (H492Q +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2040818	NM_182643.3(DLC1):c.2996G>A (p.Arg999Gln)	DLC1 (R607Q +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2064487	NM_182643.3(DLC1):c.2994C>G (p.His998Gln)	DLC1 (H487Q +7 more)	Single nucleotide variant (missense variant)	DLC1-related disorder +1 more	GUncertain significance
Select item 2023017	NM_182643.3(DLC1):c.2991-4G>A	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 712010	NM_182643.3(DLC1):c.2991-5C>G	DLC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2917667	NM_182643.3(DLC1):c.2991-8T>C	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2876848	NM_182643.3(DLC1):c.2991-19del	DLC1	Deletion (intron variant)	not provided	GLikely benign
Select item 2694236	NM_182643.3(DLC1):c.2991-20C>A	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1973102	NM_182643.3(DLC1):c.2990+20C>A	DLC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1971003	NM_182643.3(DLC1):c.2990+20C>T	DLC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2001739	NM_182643.3(DLC1):c.2976A>T (p.Leu992=)	DLC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2092058	NM_182643.3(DLC1):c.2933C>G (p.Ser978Cys)	DLC1 (S978C +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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