"Baylor Genetics"[submitter] AND "MEN1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 3241914	NM_001370259.2(MEN1):c.1778C>T (p.Ser593Phe)	MEN1 (S538F +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
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 3241912	NM_001370259.2(MEN1):c.1760T>G (p.Met587Arg)	MEN1 (M532R +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
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 485724	NM_001370259.2(MEN1):c.1699G>C (p.Ala567Pro)	MEN1 (A567P +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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 959531	NM_001370259.2(MEN1):c.1648G>T (p.Val550Leu)	MEN1 (V555L +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 640403	NM_001370259.2(MEN1):c.1648G>C (p.Val550Leu)	MEN1 (V550L +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 188066	NM_001370259.2(MEN1):c.1637C>T (p.Pro546Leu)	MEN1 (P546L +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 136167	NM_001370259.2(MEN1):c.1594G>T (p.Gly532Cys)	MEN1 (G532C +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 3241910	NM_001370259.2(MEN1):c.1588G>A (p.Glu530Lys)	MEN1 (E475K +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 426212	NM_001370259.2(MEN1):c.1580G>A (p.Arg527Gln)	MEN1 (R527Q +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 651907	NM_001370259.2(MEN1):c.1547G>A (p.Arg516Gln)	MEN1 (R481Q +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 241809	NM_001370259.2(MEN1):c.1541C>G (p.Pro514Arg)	MEN1 (P514R +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 403081	NM_001370259.2(MEN1):c.1522C>A (p.Gln508Lys)	MEN1 (Q508K +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GConflicting classifications of pathogenicity
Select item 3241911	NM_001370259.2(MEN1):c.1502_1513del (p.Asp501_Leu504del)	MEN1	Deletion (inframe_deletion +2 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2676505	NM_001370259.2(MEN1):c.1502A>T (p.Asp501Val)	MEN1 (D446V +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 457303	NM_001370259.2(MEN1):c.1478C>T (p.Pro493Leu)	MEN1 (P493L +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 3241909	NM_001370259.2(MEN1):c.1473G>T (p.Glu491Asp)	MEN1 (E436D +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 134641	NM_001370259.2(MEN1):c.1465C>T (p.Pro489Ser)	MEN1 (P489S +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2150522	NM_001370259.2(MEN1):c.1441C>T (p.Arg481Trp)	MEN1 (R481W +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 1006845	NM_001370259.2(MEN1):c.1427G>A (p.Arg476Gln)	MEN1 (R441Q +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2676515	NM_001370259.2(MEN1):c.1397_1410del (p.Glu466fs)	MEN1 (E411fs +6 more)	Deletion (frameshift variant +1 more)	Multiple endocrine neoplasia, type 1	GLikely pathogenic
Select item 659182	NM_001370259.2(MEN1):c.1391_1405del (p.Ala464_Glu468del)	MEN1	Deletion (inframe_deletion)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2676510	NM_001370259.2(MEN1):c.1399G>T (p.Ala467Ser)	MEN1 (A412S +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 403798	NM_001370259.2(MEN1):c.1399G>A (p.Ala467Thr)	MEN1 (A472T +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 457294	NM_001370259.2(MEN1):c.1398G>T (p.Glu466Asp)	MEN1 (E466D +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 950710	NM_001370259.2(MEN1):c.1387G>A (p.Glu463Lys)	MEN1 (E428K +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 403834	NM_001370259.2(MEN1):c.1379G>C (p.Arg460Pro)	MEN1 (R460P +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 41850	NM_001370259.2(MEN1):c.1379G>A (p.Arg460Gln)	MEN1 (R460Q +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2874931	NM_001370259.2(MEN1):c.1373T>C (p.Val458Ala)	MEN1 (V403A +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 527252	NM_001370259.2(MEN1):c.1367G>A (p.Arg456His)	MEN1 (R456H +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GConflicting classifications of pathogenicity
Select item 2676506	NM_001370259.2(MEN1):c.1366C>A (p.Arg456Ser)	MEN1 (R401S +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 848216	NM_001370259.2(MEN1):c.1366C>T (p.Arg456Cys)	MEN1 (R421C +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 36523	NM_001370259.2(MEN1):c.1262G>A (p.Cys421Tyr)	MEN1 (C421Y +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GPathogenic/Likely pathogenic
Select item 428090	NM_001370259.2(MEN1):c.1247_1254del (p.Phe416fs)	MEN1 (F381fs +3 more)	Deletion (frameshift variant)	Multiple endocrine neoplasia, type 1 +1 more	GPathogenic/Likely pathogenic
Select item 16703	NM_001370259.2(MEN1):c.1252G>A (p.Asp418Asn)	MEN1 (D418N +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GPathogenic
Select item 241797	NM_001370259.2(MEN1):c.1202G>T (p.Gly401Val)	MEN1 (G401V +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 818565	NM_001370259.2(MEN1):c.1192C>G (p.Gln398Glu)	MEN1 (Q403E +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 646507	NM_001370259.2(MEN1):c.1166G>C (p.Arg389Pro)	MEN1 (R389P +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 220268	NM_001370259.2(MEN1):c.1166G>A (p.Arg389Gln)	MEN1 (R394Q +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 403809	NM_001370259.2(MEN1):c.1165C>T (p.Arg389Trp)	MEN1 (R394W +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 1737468	NM_001370259.2(MEN1):c.1163A>G (p.Glu388Gly)	MEN1 (E388G +5 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 403823	NM_001370259.2(MEN1):c.1159G>A (p.Glu387Lys)	MEN1 (E392K +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 220084	NM_001370259.2(MEN1):c.1157G>A (p.Gly386Asp)	MEN1 (G391D +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 527247	NM_001370259.2(MEN1):c.1154C>T (p.Ala385Val)	MEN1 (A385V +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 933592	NM_001370259.2(MEN1):c.1138G>A (p.Ala380Thr)	MEN1 (A422T +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 2676512	NM_001370259.2(MEN1):c.1126C>A (p.Leu376Met)	MEN1 (L341M +5 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 1797816	NM_001370259.2(MEN1):c.1121A>C (p.Asn374Thr)	MEN1 (N339T +5 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1460516	NM_001370259.2(MEN1):c.1117C>A (p.Pro373Thr)	MEN1 (P338T +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 183065	NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp)	MEN1 (E366D +3 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2676514	NM_001370259.2(MEN1):c.1055A>G (p.Asn352Ser)	MEN1 (N317S +5 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 2500676	NM_001370259.2(MEN1):c.1050-3C>G	MEN1	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 1 +2 more	GConflicting classifications of pathogenicity
Select item 527268	NM_001370259.2(MEN1):c.1049+1G>A	MEN1	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 3241913	NM_001370259.2(MEN1):c.1039G>A (p.Val347Ile)	MEN1 (V312I +2 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 457276	NM_001370259.2(MEN1):c.1025C>T (p.Ala342Val)	MEN1 (A342V +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 403808	NM_001370259.2(MEN1):c.1012C>G (p.Leu338Val)	MEN1 (L338V +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 457274	NM_001370259.2(MEN1):c.1003C>T (p.Arg335Trp)	MEN1 (R335W +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 485723	NM_001370259.2(MEN1):c.989G>A (p.Arg330His)	MEN1 (R330H +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 428049	NM_001370259.2(MEN1):c.970del (p.Leu324fs)	MEN1 (L329fs +2 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 457348	NM_001370259.2(MEN1):c.964A>T (p.Met322Leu)	MEN1 (M322L +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 1041464	NM_001370259.2(MEN1):c.958C>T (p.Pro320Ser)	MEN1 (P320S +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 1524328	NM_001370259.2(MEN1):c.949C>T (p.His317Tyr)	MEN1 (H317Y +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 849297	NM_001370259.2(MEN1):c.940C>T (p.Arg314Trp)	MEN1 (R314W +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 941478	NM_001370259.2(MEN1):c.899C>T (p.Thr300Ile)	MEN1 (T265I +2 more)	Single nucleotide variant (missense variant)	Diffuse midline glioma, H3 K27-altered +2 more	GUncertain significance
Select item 457342	NM_001370259.2(MEN1):c.869A>C (p.Glu290Ala)	MEN1 (E290A +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 643929	NM_001370259.2(MEN1):c.839T>C (p.Leu280Ser)	MEN1 (L245S +2 more)	Single nucleotide variant (missense variant)	MEN1-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 827450	NM_001370259.2(MEN1):c.809T>C (p.Leu270Pro)	MEN1 (L275P +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GUncertain significance
Select item 485718	NM_001370259.2(MEN1):c.785A>G (p.Lys262Arg)	MEN1 (K262R +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 41855	NM_001370259.2(MEN1):c.774G>C (p.Gln258His)	MEN1 (Q258H +2 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 201012	NM_001370259.2(MEN1):c.758C>T (p.Ser253Leu)	MEN1 (S253L +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GConflicting classifications of pathogenicity
Select item 581204	NM_001370259.2(MEN1):c.754G>C (p.Asp252His)	MEN1 (D252H +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2676508	NM_001370259.2(MEN1):c.751A>G (p.Thr251Ala)	MEN1 (T216A +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 457336	NM_001370259.2(MEN1):c.736T>G (p.Ser246Ala)	MEN1 (S251A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 403803	NM_001370259.2(MEN1):c.710C>T (p.Ala237Val)	MEN1 (A237V +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 946791	NM_001370259.2(MEN1):c.700A>T (p.Met234Leu)	MEN1 (M199L +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 852290	NM_001370259.2(MEN1):c.691G>C (p.Asp231His)	MEN1 (D231H +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 241823	NM_001370259.2(MEN1):c.686G>A (p.Arg229His)	MEN1 (R229H +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 403826	NM_001370259.2(MEN1):c.682A>G (p.Met228Val)	MEN1 (M228V +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GUncertain significance
Select item 265236	NM_001370259.2(MEN1):c.668T>C (p.Leu223Pro)	MEN1 (L223P +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GPathogenic
Select item 241821	NM_001370259.2(MEN1):c.655-5C>G	MEN1	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 826470	NM_001370259.2(MEN1):c.653G>A (p.Arg218Gln)	MEN1 (R218Q +1 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2676511	NM_001370259.2(MEN1):c.638C>G (p.Ala213Gly)	MEN1 (A213G +1 more)	Single nucleotide variant (missense variant +2 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 527258	NM_001370259.2(MEN1):c.635A>G (p.Asn212Ser)	MEN1 (N212S +1 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1 +3 more	GUncertain significance
Select item 942293	NM_001370259.2(MEN1):c.619A>G (p.Arg207Gly)	MEN1 (R207G +1 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2676503	NM_001370259.2(MEN1):c.577A>G (p.Thr193Ala)	MEN1 (T193A +1 more)	Single nucleotide variant (missense variant +2 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 527273	NM_001370259.2(MEN1):c.568G>A (p.Gly190Arg)	MEN1 (G195R +1 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 136170	NM_001370259.2(MEN1):c.566A>G (p.Asn189Ser)	MEN1 (N189S +1 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1 +2 more	GConflicting classifications of pathogenicity
Select item 825603	NM_001370259.2(MEN1):c.526G>A (p.Ala176Thr)	MEN1 (A176T +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GUncertain significance
Select item 485714	NM_001370259.2(MEN1):c.526G>T (p.Ala176Ser)	MEN1 (A176S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 527277	NM_001370259.2(MEN1):c.485T>C (p.Val162Ala)	MEN1 (V162A +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +1 more	GUncertain significance
Select item 2564962	NM_001370259.2(MEN1):c.443C>T (p.Thr148Ile)	MEN1 (T148I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2676509	NM_001370259.2(MEN1):c.432C>G (p.Phe144Leu)	MEN1 (F144L)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 527260	NM_001370259.2(MEN1):c.418A>T (p.Ile140Phe)	MEN1 (I140F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1510715	NM_001370259.2(MEN1):c.367G>A (p.Asp123Asn)	MEN1 (D123N)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1	GUncertain significance
Select item 216817	NM_001370259.2(MEN1):c.361G>A (p.Val121Ile)	MEN1 (V121I)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GUncertain significance
Select item 201019	NM_001370259.2(MEN1):c.355AAG[1] (p.Lys120del)	MEN1 (K120del)	Microsatellite (inframe_deletion)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 428047	NM_001370259.2(MEN1):c.344G>A (p.Arg115His)	MEN1 (R115H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance

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