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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 755999	NM_000208.4(INSR):c.4134G>C (p.Arg1378=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1685300	NM_000208.4(INSR):c.4133G>A (p.Arg1378Gln)	INSR (R1366Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2772535	NM_000208.4(INSR):c.4121T>G (p.Leu1374Arg)	INSR (L1362R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1972379	NM_000208.4(INSR):c.4086A>G (p.Thr1362=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 330438	NM_000208.4(INSR):c.4082A>G (p.Tyr1361Cys)	INSR (Y1361C +1 more)	Single nucleotide variant (missense variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +3 more	GConflicting classifications of pathogenicity
Select item 1643540	NM_000208.4(INSR):c.4044G>C (p.Ser1348=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 734788	NM_000208.4(INSR):c.3999G>T (p.Ser1333=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 733399	NM_000208.4(INSR):c.3999G>A (p.Ser1333=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2144562	NM_000208.4(INSR):c.3991C>T (p.Arg1331Cys)	INSR (R1319C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1486096	NM_000208.4(INSR):c.3937G>A (p.Glu1313Lys)	INSR (E1301K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2634452	NM_000208.4(INSR):c.3919G>A (p.Glu1307Lys)	INSR (E1295K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2085323	NM_000208.4(INSR):c.3918C>T (p.Ser1306=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 759511	NM_000208.4(INSR):c.3876C>T (p.Asp1292=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 808429	NM_000208.4(INSR):c.3809G>A (p.Arg1270His)	INSR (R1258H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 498092	NM_000208.4(INSR):c.3805A>T (p.Met1269Leu)	INSR (M1269L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 330440	NM_000208.4(INSR):c.3795-5C>T	INSR	Single nucleotide variant (intron variant)	Rabson-Mendenhall syndrome +3 more	GBenign
Select item 435517	NM_000208.4(INSR):c.3775G>A (p.Asp1259Asn)	INSR (D1259N +1 more)	Single nucleotide variant (missense variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +5 more	GUncertain significance/Uncertain risk allele
Select item 737288	NM_000208.4(INSR):c.3694T>C (p.Leu1232=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2740782	NM_000208.4(INSR):c.3633_3634del (p.Val1212fs)	INSR (V1212fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 721240	NM_000208.4(INSR):c.3615G>A (p.Pro1205=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1480867	NM_000208.4(INSR):c.3614C>T (p.Pro1205Leu)	INSR (P1205L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 14709	NM_000208.4(INSR):c.3540G>A (p.Met1180Ile)	INSR (M1168I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1633572	NM_000208.4(INSR):c.3530-15C>A	INSR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2012772	NM_000208.4(INSR):c.3489A>C (p.Arg1163Ser)	INSR (R1163S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2736766	NM_000208.4(INSR):c.3472C>T (p.Arg1158Trp)	INSR (R1158W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1330899	NM_000208.4(INSR):c.3470A>G (p.His1157Arg)	INSR (H1145R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2919737	NM_000208.4(INSR):c.3465T>C (p.Phe1155=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2887735	NM_000208.4(INSR):c.3435C>T (p.Asp1145=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 435516	NM_000208.4(INSR):c.3410T>C (p.Ile1137Thr)	INSR (I1137T +1 more)	Single nucleotide variant (missense variant)	not provided +5 more	GUncertain significance
Select item 330445	NM_000208.4(INSR):c.3370-15G>A	INSR	Single nucleotide variant (intron variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +3 more	GBenign/Likely benign
Select item 3022949	NM_000208.4(INSR):c.3370-16C>G	INSR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957365	NM_000208.4(INSR):c.3370-16C>T	INSR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 752910	NM_000208.4(INSR):c.3324C>T (p.His1108=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1552321	NM_000208.4(INSR):c.3321T>C (p.Ala1107=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 733855	NM_000208.4(INSR):c.3297G>A (p.Thr1099=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1629616	NM_000208.4(INSR):c.3258+16G>A	INSR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 194701	NM_000208.4(INSR):c.3255C>T (p.His1085=)	INSR	Single nucleotide variant (synonymous variant)	Leprechaunism syndrome +4 more	GBenign
Select item 732875	NM_000208.4(INSR):c.3228G>A (p.Ser1076=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2858657	NM_000208.4(INSR):c.3203G>A (p.Arg1068Gln)	INSR (R1068Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1336219	NM_000208.4(INSR):c.3202C>T (p.Arg1068Trp)	INSR (R1056W +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 723728	NM_000208.4(INSR):c.3174G>A (p.Thr1058=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 286413	NM_000208.4(INSR):c.3165G>A (p.Ala1055=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 2414166	NM_000208.4(INSR):c.3157C>T (p.Arg1053Cys)	INSR (R1041C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1928260	NM_000208.4(INSR):c.3138C>A (p.Ile1046=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 741192	NM_000208.4(INSR):c.3102C>T (p.Phe1034=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 14707	NM_000208.4(INSR):c.3034G>A (p.Val1012Met)	INSR (V1012M +1 more)	Single nucleotide variant (missense variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +6 more	GConflicting classifications of pathogenicity
Select item 330447	NM_000208.4(INSR):c.3033C>T (p.Tyr1011=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +4 more	GBenign
Select item 211196	NM_000208.4(INSR):c.2971C>A (p.Leu991Ile)	INSR (L991I +1 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 281873	NM_000208.4(INSR):c.2970G>A (p.Pro990=)	INSR	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 330448	NM_000208.4(INSR):c.2946-14T>C	INSR	Single nucleotide variant (intron variant)	Rabson-Mendenhall syndrome +4 more	GBenign/Likely benign
Select item 1953365	NM_000208.4(INSR):c.2946-20G>A	INSR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 330449	NM_000208.4(INSR):c.2933T>A (p.Phe978Tyr)	INSR (F978Y +1 more)	Single nucleotide variant (missense variant)	Rabson-Mendenhall syndrome +3 more	GUncertain significance
Select item 2785362	NM_000208.4(INSR):c.2901C>T (p.Leu967=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 330450	NM_000208.4(INSR):c.2853G>A (p.Pro951=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +3 more	GConflicting classifications of pathogenicity
Select item 211195	NM_000208.4(INSR):c.2838C>G (p.Asp946Glu)	INSR (D946E +1 more)	Single nucleotide variant (missense variant)	Leprechaunism syndrome +5 more	GConflicting classifications of pathogenicity
Select item 892834	NM_000208.4(INSR):c.2829C>T (p.Tyr943=)	INSR	Single nucleotide variant (synonymous variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +4 more	GConflicting classifications of pathogenicity
Select item 744791	NM_000208.4(INSR):c.2799C>T (p.Asn933=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 739582	NM_000208.4(INSR):c.2793G>A (p.Ala931=)	INSR	Single nucleotide variant (synonymous variant)	Hyperinsulinism due to INSR deficiency +5 more	GConflicting classifications of pathogenicity
Select item 1623581	NM_000208.4(INSR):c.2775C>A (p.Ile925=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1510305	NM_000208.4(INSR):c.2767G>A (p.Val923Met)	INSR (V923M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1555426	NM_000208.4(INSR):c.2754G>A (p.Pro918=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2792404	NM_000208.4(INSR):c.2741G>A (p.Arg914His)	INSR (R914H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2900446	NM_000208.4(INSR):c.2740C>T (p.Arg914Cys)	INSR (R914C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 211194	NM_000208.4(INSR):c.2736G>A (p.Arg912=)	INSR	Single nucleotide variant (synonymous variant)	Hyperinsulinism due to INSR deficiency +5 more	GConflicting classifications of pathogenicity
Select item 330451	NM_000208.4(INSR):c.2718T>C (p.Ala906=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +4 more	GBenign/Likely benign
Select item 893925	NM_000208.4(INSR):c.2698G>A (p.Val900Ile)	INSR (V900I +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 728985	NM_000208.4(INSR):c.2683-5C>T	INSR	Single nucleotide variant (intron variant)	not specified +5 more	GBenign/Likely benign
Select item 330452	NM_000208.4(INSR):c.2682+9C>G	INSR	Single nucleotide variant (intron variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +4 more	GBenign/Likely benign
Select item 2055672	NM_000208.4(INSR):c.2682+6G>T	INSR	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1976624	NM_000208.4(INSR):c.2674G>A (p.Gly892Ser)	INSR (G892S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 282255	NM_000208.4(INSR):c.2665C>T (p.Arg889Trp)	INSR (R889W +1 more)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 330453	NM_000208.4(INSR):c.2643C>T (p.Ile881=)	INSR	Single nucleotide variant (synonymous variant)	Insulin-resistant diabetes mellitus AND acanthosis nigricans +4 more	GBenign/Likely benign
Select item 211193	NM_000208.4(INSR):c.2598C>T (p.Val866=)	INSR	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 330454	NM_000208.4(INSR):c.2595C>T (p.Asn865=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +3 more	GBenign
Select item 724119	NM_000208.4(INSR):c.2575C>T (p.His859Tyr)	INSR (H847Y +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2911769	NM_000208.4(INSR):c.2574G>A (p.Thr858=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 330455	NM_000208.4(INSR):c.2573C>T (p.Thr858Met)	INSR (T858M +1 more)	Single nucleotide variant (missense variant)	Rabson-Mendenhall syndrome +6 more	GConflicting classifications of pathogenicity
Select item 330457	NM_000208.4(INSR):c.2542+3A>G	INSR	Single nucleotide variant (intron variant)	Rabson-Mendenhall syndrome +3 more	GBenign
Select item 330458	NM_000208.4(INSR):c.2526G>C (p.Ala842=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +3 more	GBenign
Select item 2882307	NM_000208.4(INSR):c.2518G>A (p.Val840Ile)	INSR (V840I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 731479	NM_000208.4(INSR):c.2517C>T (p.Tyr839=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2229488	NM_000208.4(INSR):c.2456G>A (p.Arg819His)	INSR (R819H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 330460	NM_000208.4(INSR):c.2448G>A (p.Thr816=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +3 more	GBenign
Select item 549552	NM_000208.4(INSR):c.2388G>C (p.Arg796Ser)	INSR (R796S +1 more)	Single nucleotide variant (missense variant)	Rabson-Mendenhall syndrome +6 more	GConflicting classifications of pathogenicity
Select item 797187	NM_000208.4(INSR):c.2376G>A (p.Pro792=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2716762	NM_000208.4(INSR):c.2375C>T (p.Pro792Leu)	INSR (P780L +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 330461	NM_000208.4(INSR):c.2370G>A (p.Thr790=)	INSR	Single nucleotide variant (synonymous variant)	Rabson-Mendenhall syndrome +3 more	GBenign
Select item 742548	NM_000208.4(INSR):c.2361C>T (p.Ser787=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 211192	NM_000208.4(INSR):c.2355G>A (p.Ser785=)	INSR	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2419909	NM_000208.4(INSR):c.2328G>A (p.Thr776=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 750057	NM_000208.4(INSR):c.2325C>T (p.Pro775=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2715332	NM_000208.4(INSR):c.2320G>A (p.Val774Met)	INSR (V762M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 732281	NM_000208.4(INSR):c.2319C>T (p.Ala773=)	INSR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970962	NM_000208.4(INSR):c.2296G>A (p.Asp766Asn)	INSR (D754N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 330462	NM_000208.4(INSR):c.2295C>T (p.Gly765=)	INSR	Single nucleotide variant (synonymous variant)	Hyperinsulinism due to INSR deficiency +5 more	GConflicting classifications of pathogenicity
Select item 810984	NM_000208.4(INSR):c.2267+17C>T	INSR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 796295	NM_000208.4(INSR):c.2263C>T (p.Pro755Ser)	INSR (P755S)	Single nucleotide variant (missense variant +1 more)	Rabson-Mendenhall syndrome +4 more	GConflicting classifications of pathogenicity
Select item 597779	NM_000208.4(INSR):c.2256C>G (p.Ala752=)	INSR	Single nucleotide variant (synonymous variant +1 more)	not provided	GConflicting classifications of pathogenicity
Select item 720063	NM_000208.4(INSR):c.2250T>C (p.Thr750=)	INSR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 211190	NM_000208.4(INSR):c.2243C>T (p.Ser748Leu)	INSR (S748L)	Single nucleotide variant (missense variant +1 more)	Leprechaunism syndrome +6 more	GConflicting classifications of pathogenicity

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