C0025267[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 572762	NM_130799.2(MEN1):c.1351_*820del (p.Val451fs)	MEN1 (V451fs)	Deletion	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 417317	NC_000011.10:g.(?_64803514)_(64804816_?)del	MEN1	Deletion	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 417316	NC_000011.10:g.(?_64803514)_(64810132_?)del	MEN1	Deletion	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 580649	NM_001370259.2(MEN1):c.1351-2_*132del	MEN1	Deletion (splice acceptor variant)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 655218	NC_000011.10:g.(?_64804324)_(64810716_?)del	MEN1	Deletion	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 2815238	NM_001370259.2(MEN1):c.1831_1832del (p.Ter611AsnextTer?)	MEN1	Deletion (frameshift variant +2 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2761444	NM_001370259.2(MEN1):c.1830C>G (p.Leu610=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 1014223	NM_001370259.2(MEN1):c.1828C>T (p.Leu610Phe)	MEN1 (L575F +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 527289	NM_001370259.2(MEN1):c.1826G>T (p.Gly609Val)	MEN1 (G614V +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 1487775	NM_001370259.2(MEN1):c.1822A>G (p.Lys608Glu)	MEN1 (K608E +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1581065	NM_001370259.2(MEN1):c.1821C>T (p.Arg607=)	MEN1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2755858	NM_001370259.2(MEN1):c.1819C>A (p.Arg607Ser)	MEN1 (R552S +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1008780	NM_001370259.2(MEN1):c.1819C>T (p.Arg607Cys)	MEN1 (R572C +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1920616	NM_001370259.2(MEN1):c.1818G>A (p.Gln606=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 940093	NM_001370259.2(MEN1):c.1814G>T (p.Arg605Leu)	MEN1 (R605L +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 200992	NM_001370259.2(MEN1):c.1814G>A (p.Arg605Gln)	MEN1 (R605Q +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1378004	NM_001370259.2(MEN1):c.1813C>G (p.Arg605Gly)	MEN1 (R610G +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2134642	NM_001370259.2(MEN1):c.1812G>C (p.Lys604Asn)	MEN1 (K604N +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 955094	NM_001370259.2(MEN1):c.1805dup (p.Leu603fs)	MEN1 (L568fs +3 more)	Duplication (frameshift variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 412571	NM_001370259.2(MEN1):c.1806C>T (p.Phe602=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 2693380	NM_001370259.2(MEN1):c.1798_1803del (p.Leu600_Ser601del)	MEN1	Deletion (inframe_deletion +1 more)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 1720343	NM_001370259.2(MEN1):c.1802C>G (p.Ser601Cys)	MEN1 (S546C +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2000284	NM_001370259.2(MEN1):c.1800_1801del (p.Ser601fs)	MEN1 (S566fs +3 more)	Deletion (frameshift variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1013726	NM_001370259.2(MEN1):c.1801T>C (p.Ser601Pro)	MEN1 (S566P +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2007820	NM_001370259.2(MEN1):c.1800G>A (p.Leu600=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1962891	NM_001370259.2(MEN1):c.1800G>C (p.Leu600=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 457316	NM_001370259.2(MEN1):c.1800G>T (p.Leu600=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +2 more	GLikely benign
Select item 457315	NM_001370259.2(MEN1):c.1798_1799del (p.Leu600fs)	MEN1 (L605fs +3 more)	Microsatellite (frameshift variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1131294	NM_001370259.2(MEN1):c.1798C>T (p.Leu600=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 1151272	NM_001370259.2(MEN1):c.1797T>C (p.Thr599=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 2624633	NM_001370259.2(MEN1):c.1795A>T (p.Thr599Ser)	MEN1 (T604S +6 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1008251	NM_001370259.2(MEN1):c.1795A>G (p.Thr599Ala)	MEN1 (T564A +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1109078	NM_001370259.2(MEN1):c.1794C>T (p.Tyr598=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 2756461	NM_001370259.2(MEN1):c.1792T>C (p.Tyr598His)	MEN1 (Y645H +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1897053	NM_001370259.2(MEN1):c.1790A>C (p.Asp597Ala)	MEN1 (D562A +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1414313	NM_001370259.2(MEN1):c.1787G>C (p.Ser596Thr)	MEN1 (S596T +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1359596	NM_001370259.2(MEN1):c.1784C>G (p.Pro595Arg)	MEN1 (P560R +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1496704	NM_001370259.2(MEN1):c.1783C>T (p.Pro595Ser)	MEN1 (P595S +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2829382	NM_001370259.2(MEN1):c.1782C>T (p.Thr594=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 2113688	NM_001370259.2(MEN1):c.1780A>C (p.Thr594Pro)	MEN1 (T594P +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 457314	NM_001370259.2(MEN1):c.1779C>T (p.Ser593=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 575287	NM_001370259.2(MEN1):c.1777T>C (p.Ser593Pro)	MEN1 (S593P +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 1525376	NM_001370259.2(MEN1):c.1775T>C (p.Val592Ala)	MEN1 (V597A +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2870969	NM_001370259.2(MEN1):c.1770G>A (p.Gln590=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 1350235	NM_001370259.2(MEN1):c.1770G>C (p.Gln590His)	MEN1 (Q595H +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 573100	NM_001370259.2(MEN1):c.1762AAG[1] (p.Lys589del)	MEN1 (K589del +3 more)	Microsatellite (inframe_deletion)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2761267	NM_001370259.2(MEN1):c.1766A>T (p.Lys589Met)	MEN1 (K554M +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 215962	NM_001370259.2(MEN1):c.1764G>A (p.Lys588=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +3 more	GConflicting classifications of pathogenicity
Select item 457313	NM_001370259.2(MEN1):c.1761G>A (p.Met587Ile)	MEN1 (M587I +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 527305	NM_001370259.2(MEN1):c.1758G>A (p.Gln586=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 2095800	NM_001370259.2(MEN1):c.1756C>T (p.Gln586Ter)	MEN1 (Q531* +6 more)	Single nucleotide variant (nonsense)	Multiple endocrine neoplasia, type 1	GLikely pathogenic
Select item 1155689	NM_001370259.2(MEN1):c.1755G>A (p.Val585=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 1038249	NM_001370259.2(MEN1):c.1754T>A (p.Val585Glu)	MEN1 (V627E +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 659280	NM_001370259.2(MEN1):c.1754T>G (p.Val585Gly)	MEN1 (V590G +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1158914	NM_001370259.2(MEN1):c.1749G>T (p.Ser583=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 457312	NM_001370259.2(MEN1):c.1749G>C (p.Ser583=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 772039	NM_001370259.2(MEN1):c.1740G>A (p.Thr580=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 428074	NM_001370259.2(MEN1):c.1740G>C (p.Thr580=)	MEN1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 2702778	NM_001370259.2(MEN1):c.1738_1739insAA (p.Thr580fs)	MEN1 (T622fs +6 more)	Insertion (frameshift variant +1 more)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 942429	NM_001370259.2(MEN1):c.1739C>T (p.Thr580Met)	MEN1 (T545M +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 220647	NM_001370259.2(MEN1):c.1739del (p.Thr580fs)	MEN1 (T545fs +3 more)	Deletion (frameshift variant)	Multiple endocrine neoplasia, type 1	GLikely pathogenic
Select item 853356	NM_001370259.2(MEN1):c.1735C>T (p.Leu579Phe)	MEN1 (L544F +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2137137	NM_001370259.2(MEN1):c.1732C>T (p.Gln578Ter)	MEN1 (Q523* +6 more)	Single nucleotide variant (nonsense)	not provided +1 more	GLikely pathogenic
Select item 200991	NM_001370259.2(MEN1):c.1730T>C (p.Leu577Pro)	MEN1 (L577P +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 751521	NM_001370259.2(MEN1):c.1729C>T (p.Leu577=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 956349	NM_001370259.2(MEN1):c.1727A>C (p.Lys576Thr)	MEN1 (K618T +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1463994	NM_001370259.2(MEN1):c.1725C>G (p.Ile575Met)	MEN1 (I617M +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2863348	NM_001370259.2(MEN1):c.1724T>C (p.Ile575Thr)	MEN1 (I617T +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1721076	NM_001370259.2(MEN1):c.1720G>A (p.Ala574Thr)	MEN1 (A519T +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2455741	NM_001370259.2(MEN1):c.1719C>T (p.Ser573=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 942761	NM_001370259.2(MEN1):c.1718G>A (p.Ser573Asn)	MEN1 (S573N +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1778635	NM_001370259.2(MEN1):c.1716G>A (p.Ser572=)	MEN1	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 1554219	NM_001370259.2(MEN1):c.1713C>T (p.Asn571=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 2863013	NM_001370259.2(MEN1):c.1705_1706del (p.Lys569fs)	MEN1 (K534fs +6 more)	Deletion (frameshift variant +1 more)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 2093340	NM_001370259.2(MEN1):c.1705A>G (p.Lys569Glu)	MEN1 (K534E +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1039168	NM_001370259.2(MEN1):c.1703C>G (p.Thr568Ser)	MEN1 (T533S +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 848775	NM_001370259.2(MEN1):c.1703C>T (p.Thr568Ile)	MEN1 (T533I +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 2767024	NM_001370259.2(MEN1):c.1702A>G (p.Thr568Ala)	MEN1 (T573A +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 428038	NM_001370259.2(MEN1):c.1701C>T (p.Ala567=)	MEN1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 485724	NM_001370259.2(MEN1):c.1699G>C (p.Ala567Pro)	MEN1 (A567P +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 1135579	NM_001370259.2(MEN1):c.1698G>A (p.Val566=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 1778258	NM_001370259.2(MEN1):c.1697T>C (p.Val566Ala)	MEN1 (V571A +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 241810	NM_001370259.2(MEN1):c.1695G>T (p.Leu565=)	MEN1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1088628	NM_001370259.2(MEN1):c.1693C>T (p.Leu565=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 527298	NM_001370259.2(MEN1):c.1692G>T (p.Leu564=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 1508010	NM_001370259.2(MEN1):c.1691T>C (p.Leu564Pro)	MEN1 (L529P +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1141204	NM_001370259.2(MEN1):c.1689G>A (p.Glu563=)	MEN1	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1610024	NM_001370259.2(MEN1):c.1686G>A (p.Lys562=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 1399276	NM_001370259.2(MEN1):c.1682T>C (p.Met561Thr)	MEN1 (M603T +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 859580	NM_001370259.2(MEN1):c.1672_1679del (p.Met558fs)	MEN1 (M563fs +3 more)	Deletion (frameshift variant)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 1607463	NM_001370259.2(MEN1):c.1677G>A (p.Lys559=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1 +1 more	GLikely benign
Select item 569154	NM_001370259.2(MEN1):c.1674dup (p.Lys559fs)	MEN1 (K524fs +3 more)	Duplication (frameshift variant)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 1777760	NM_001370259.2(MEN1):c.1674G>A (p.Met558Ile)	MEN1 (M558I +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2808810	NM_001370259.2(MEN1):c.1673T>C (p.Met558Thr)	MEN1 (M523T +6 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 2080505	NM_001370259.2(MEN1):c.1642_1673delinsCC (p.Gly548_Met558delinsPro)	MEN1	Indel (inframe_indel)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 201023	NM_001370259.2(MEN1):c.1667AGA[1] (p.Lys557del)	MEN1 (K557del +3 more)	Microsatellite (inframe_deletion)	MEN1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1717267	NM_001370259.2(MEN1):c.1670A>T (p.Lys557Met)	MEN1 (K502M +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 666173	NM_001370259.2(MEN1):c.1670del (p.Lys557fs)	MEN1 (K557fs +3 more)	Deletion (frameshift variant)	Multiple endocrine neoplasia, type 1	GPathogenic
Select item 1117370	NM_001370259.2(MEN1):c.1668G>A (p.Glu556=)	MEN1	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 1	GLikely benign
Select item 216134	NM_001370259.2(MEN1):c.1664G>A (p.Ser555Asn)	MEN1 (S555N +3 more)	Single nucleotide variant (missense variant)	not specified +3 more	GPathogenic/Likely pathogenic

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