MAX[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 313788	NM_002382.5(MAX):c.*1308C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313789	NM_002382.5(MAX):c.*1285T>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313790	NM_002382.5(MAX):c.*1278C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313791	NM_002382.5(MAX):c.*1276G>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313792	NM_002382.5(MAX):c.*1229C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313793	NM_002382.5(MAX):c.*1127G>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma +1 more	GBenign
Select item 313794	NM_002382.5(MAX):c.*1123A>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 883970	NM_002382.5(MAX):c.*1035C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313795	NM_002382.5(MAX):c.*1023C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 880680	NM_002382.5(MAX):c.*943G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313796	NM_002382.5(MAX):c.*942C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313797	NM_002382.5(MAX):c.*873T>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313798	NM_002382.5(MAX):c.*717T>C	MAX	Single nucleotide variant (intron variant +1 more)	Pheochromocytoma +1 more	GBenign
Select item 880681	NM_002382.5(MAX):c.*700G>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 880682	NM_002382.5(MAX):c.*678C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 880683	NM_002382.5(MAX):c.*616C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 313799	NM_002382.5(MAX):c.*608CA[1]	MAX	Microsatellite (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313800	NM_002382.5(MAX):c.*603C>G	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GLikely benign
Select item 313801	NM_002382.5(MAX):c.*587G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 313802	NM_002382.5(MAX):c.*565G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 313803	NM_002382.5(MAX):c.*534G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313804	NM_002382.5(MAX):c.*503T>G	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313805	NM_002382.5(MAX):c.*461C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 313806	NM_002382.5(MAX):c.*405G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GLikely benign
Select item 313807	NM_002382.5(MAX):c.*404C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 313808	NM_002382.5(MAX):c.*375G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 1677325	NM_002382.5(MAX):c.*374C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 313809	NM_002382.5(MAX):c.*344T>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 313810	NM_002382.5(MAX):c.*320T>G	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313811	NM_002382.5(MAX):c.*297C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 313812	NM_002382.5(MAX):c.*248A>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 313813	NM_002382.5(MAX):c.*170C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 884037	NM_002382.5(MAX):c.*169T>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313814	NM_002382.5(MAX):c.*144C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 880742	NM_002382.5(MAX):c.*128T>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 880743	NM_002382.5(MAX):c.*96C>G	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GUncertain significance
Select item 313815	NM_002382.5(MAX):c.*92G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma +1 more	GBenign
Select item 880744	NM_002382.5(MAX):c.*65G>C	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GBenign
Select item 313816	NM_002382.5(MAX):c.*44G>A	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma	GLikely benign
Select item 313817	NM_002382.5(MAX):c.*7C>T	MAX	Single nucleotide variant (3 prime UTR variant +1 more)	Pheochromocytoma +2 more	GBenign/Likely benign
Select item 2631349	NM_002382.5(MAX):c.*2C>T	MAX	Single nucleotide variant (3 prime UTR variant +2 more)	MAX-related disorder	GUncertain significance
Select item 1743165	NM_002382.5(MAX):c.479G>T (p.Ser160Ile)	MAX (S93I +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1987900	NM_002382.5(MAX):c.478del (p.Ser160fs)	MAX (S151fs +2 more)	Deletion (frameshift variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 3222159	NM_002382.5(MAX):c.475del (p.Ala159fs)	MAX (A123fs +4 more)	Deletion (frameshift variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 825151	NM_002382.5(MAX):c.475G>A (p.Ala159Thr)	MAX (A96T +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2985228	NM_002382.5(MAX):c.474G>A (p.Glu158=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 2093029	NM_002382.5(MAX):c.473A>G (p.Glu158Gly)	MAX (E149G +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 232084	NM_002382.5(MAX):c.467G>A (p.Arg156Gln)	MAX (R156Q +4 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GUncertain significance
Select item 1742300	NM_002382.5(MAX):c.466C>G (p.Arg156Gly)	MAX (R120G +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 647774	NM_002382.5(MAX):c.466C>T (p.Arg156Trp)	MAX (R93W +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 774772	NM_002382.5(MAX):c.462G>A (p.Lys154=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2757638	NM_002382.5(MAX):c.460A>G (p.Lys154Glu)	MAX (K145E +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 3222158	NM_002382.5(MAX):c.459G>T (p.Lys153Asn)	MAX (K117N +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1099624	NM_002382.5(MAX):c.459G>A (p.Lys153=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 1878967	NM_002382.5(MAX):c.456G>C (p.Arg152Ser)	MAX (R116S +4 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1635871	NM_002382.5(MAX):c.456G>A (p.Arg152=)	MAX	Single nucleotide variant (3 prime UTR variant +3 more)	Hereditary pheochromocytoma-paraganglioma +1 more	GLikely benign
Select item 2453895	NM_002382.5(MAX):c.454A>G (p.Arg152Gly)	MAX (R152G +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2587741	NM_002382.5(MAX):c.453C>A (p.Ser151Arg)	MAX (S115R +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1366073	NM_002382.5(MAX):c.452G>A (p.Ser151Asn)	MAX (S151N +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 1636775	NM_002382.5(MAX):c.450A>G (p.Gln150=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma +1 more	GLikely benign
Select item 2818360	NM_002382.5(MAX):c.449A>G (p.Gln150Arg)	MAX (Q114R +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 1740881	NM_002382.5(MAX):c.447C>G (p.Pro149=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma +1 more	GLikely benign
Select item 3222157	NM_002382.5(MAX):c.446C>T (p.Pro149Leu)	MAX (P113L +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2116911	NM_002382.5(MAX):c.444G>A (p.Glu148=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 570685	NM_002382.5(MAX):c.442dup (p.Glu148fs)	MAX (E139fs +2 more)	Duplication (frameshift variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 959467	NM_002382.5(MAX):c.439G>A (p.Glu147Lys)	MAX (E147K +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 2103464	NM_002382.5(MAX):c.438T>A (p.Pro146=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 1622049	NM_002382.5(MAX):c.438T>C (p.Pro146=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2630458	NM_002382.5(MAX):c.437C>G (p.Pro146Arg)	MAX (P110R +4 more)	Single nucleotide variant (missense variant +3 more)	MAX-related disorder	GUncertain significance
Select item 2178557	NM_002382.5(MAX):c.436C>T (p.Pro146Ser)	MAX (P137S +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 514278	NM_002382.5(MAX):c.435G>A (p.Glu145=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma +2 more	GLikely benign
Select item 1589933	NM_002382.5(MAX):c.432T>C (p.Ser144=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1553360	NM_002382.5(MAX):c.432T>G (p.Ser144=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 463811	NM_002382.5(MAX):c.432T>A (p.Ser144=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 1739631	NM_002382.5(MAX):c.430T>C (p.Ser144Pro)	MAX (S135P +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma +1 more	GUncertain significance
Select item 1118358	NM_002382.5(MAX):c.429G>A (p.Glu143=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 1042009	NM_002382.5(MAX):c.429G>C (p.Glu143Asp)	MAX (E80D +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma +1 more	GUncertain significance
Select item 412781	NM_002382.5(MAX):c.426G>A (p.Ser142=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 404109	NM_002382.5(MAX):c.425C>T (p.Ser142Leu)	MAX (S142L +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2751479	NM_002382.5(MAX):c.424T>C (p.Ser142Pro)	MAX (S133P +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 948950	NM_002382.5(MAX):c.422G>C (p.Ser141Thr)	MAX (S132T +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1738615	NM_002382.5(MAX):c.419C>G (p.Ser140Cys)	MAX (S77C +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1402174	NM_002382.5(MAX):c.417C>G (p.Asp139Glu)	MAX (D76E +4 more)	Single nucleotide variant (missense variant +2 more)	Pheochromocytoma +2 more	GUncertain significance
Select item 1491705	NM_002382.5(MAX):c.416A>T (p.Asp139Val)	MAX (D139V +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 404103	NM_002382.5(MAX):c.415G>A (p.Asp139Asn)	MAX (D139N +4 more)	Single nucleotide variant (missense variant +2 more)	Pheochromocytoma +3 more	GUncertain significance
Select item 2097024	NM_002382.5(MAX):c.414G>C (p.Ser138=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma	GLikely benign
Select item 404111	NM_002382.5(MAX):c.414G>A (p.Ser138=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 1059756	NM_002382.5(MAX):c.413C>T (p.Ser138Leu)	MAX (S129L +4 more)	Single nucleotide variant (missense variant +2 more)	Pheochromocytoma +2 more	GUncertain significance
Select item 1737913	NM_002382.5(MAX):c.410G>T (p.Gly137Val)	MAX (G128V +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1410024	NM_002382.5(MAX):c.410del (p.Gly137fs)	MAX (G74fs +2 more)	Deletion (frameshift variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 570366	NM_002382.5(MAX):c.410G>A (p.Gly137Asp)	MAX (G137D +4 more)	Single nucleotide variant (missense variant +2 more)	not specified +4 more	GUncertain significance
Select item 1737818	NM_002382.5(MAX):c.409G>A (p.Gly137Ser)	MAX (G101S +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1497440	NM_002382.5(MAX):c.409G>C (p.Gly137Arg)	MAX (G128R +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary pheochromocytoma-paraganglioma	GUncertain significance
Select item 1595755	NM_002382.5(MAX):c.408G>A (p.Gly136=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary pheochromocytoma-paraganglioma +2 more	GLikely benign
Select item 2568123	NM_002382.5(MAX):c.407G>A (p.Gly136Glu)	MAX (G100E +4 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1518007	NM_002382.5(MAX):c.406G>C (p.Gly136Arg)	MAX (G136R +4 more)	Single nucleotide variant (missense variant +2 more)	Pheochromocytoma +2 more	GUncertain significance
Select item 463810	NM_002382.5(MAX):c.406G>A (p.Gly136Arg)	MAX (G136R +4 more)	Single nucleotide variant (missense variant +2 more)	Pheochromocytoma +3 more	GConflicting classifications of pathogenicity
Select item 1495955	NM_002382.5(MAX):c.405T>A (p.Asp135Glu)	MAX (D72E +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1100618	NM_002382.5(MAX):c.405T>C (p.Asp135=)	MAX	Single nucleotide variant (synonymous variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 568216	NM_002382.5(MAX):c.403G>C (p.Asp135His)	MAX (D135H +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance

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