List of variants in gene MFN2 reported as benign for Charcot-Marie-Tooth disease

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 47

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HGVS	dbSNP
NM_014874.3(MFN2):c.*1100A>G	rs41278638
NM_014874.3(MFN2):c.*1161C>A	rs115706485
NM_014874.3(MFN2):c.*1258G>A	rs116156978
NM_014874.3(MFN2):c.*1488C>T	rs11554507
NM_014874.3(MFN2):c.*1546G>A	rs3737960
NM_014874.3(MFN2):c.*1562G>A	rs551566332
NM_014874.3(MFN2):c.*1576C>T	rs78523898
NM_014874.3(MFN2):c.*1706T>G	rs543365043
NM_014874.3(MFN2):c.*231G>A	rs41278636
NM_014874.3(MFN2):c.*58A>G	rs1042842
NM_014874.3(MFN2):c.*730C>T	rs112550280
NM_014874.3(MFN2):c.*777T>C	rs112854268
NM_014874.3(MFN2):c.*896G>C	rs3088064
NM_014874.3(MFN2):c.*912C>T	rs14305
NM_014874.3(MFN2):c.-161G>A	rs140094248
NM_014874.3(MFN2):c.-249T>A	rs2180182
NM_014874.3(MFN2):c.-287C>T	rs2180181
NM_014874.3(MFN2):c.-4-13G>T	rs373679523
NM_014874.3(MFN2):c.1039-19G>A	rs74052923
NM_014874.3(MFN2):c.1179G>A (p.Met393Ile)	rs12069578
NM_014874.3(MFN2):c.1452G>A (p.Thr484=)	rs150043585
NM_014874.3(MFN2):c.1495+9C>T	rs375494746
NM_014874.3(MFN2):c.150C>A (p.Ile50=)	rs78841746
NM_014874.3(MFN2):c.1569C>T (p.Ser523=)	rs1042837
NM_014874.3(MFN2):c.159C>T (p.Ser53=)	rs61733200
NM_014874.3(MFN2):c.165C>T (p.Thr55=)	rs77458527
NM_014874.3(MFN2):c.176-7C>T	rs374055101
NM_014874.3(MFN2):c.179C>T (p.Thr60Met)	rs138345244
NM_014874.3(MFN2):c.1806C>T (p.Ser602=)	rs201258935
NM_014874.3(MFN2):c.1920C>G (p.Leu640=)	rs141468012
NM_014874.3(MFN2):c.1950G>A (p.Leu650=)	rs772030424
NM_014874.3(MFN2):c.2113G>A (p.Val705Ile)	rs142271930
NM_014874.3(MFN2):c.2204+15T>C	rs77262016
NM_014874.3(MFN2):c.2205-13C>A	rs76020240
NM_014874.3(MFN2):c.474+4A>G	rs141974160
NM_014874.3(MFN2):c.522T>C (p.His174=)	rs762789747
NM_014874.3(MFN2):c.744C>T (p.Leu248=)	rs61733205
NM_014874.3(MFN2):c.891C>T (p.Ala297=)	rs11554508
NM_014874.3(MFN2):c.957C>T (p.Gly319=)	rs41278632
NM_014874.3(MFN2):c.970+19G>A	rs75865135
NM_014874.3(MFN2):c.975C>T (p.Gly325=)	rs141475476
NM_014874.4(MFN2):c.*1034C>T
NM_014874.4(MFN2):c.*1830C>T
NM_014874.4(MFN2):c.*226C>T
NM_014874.4(MFN2):c.*26G>A
NM_014874.4(MFN2):c.*304A>G
NM_014874.4(MFN2):c.-80C>T

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