List of variants reported as benign for Deficiency of malonyl-CoA decarboxylase

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_012213.3(MLYCD):c.528+19T>C	rs446036	0.96188
NM_012213.3(MLYCD):c.*412T>C	rs1127382	0.12522
NM_012213.3(MLYCD):c.*460A>C	rs1127387	0.10180
NM_012213.3(MLYCD):c.642-5C>T	rs2278037	0.07436
NM_012213.3(MLYCD):c.642-12A>T	rs2278036	0.07434
NM_012213.3(MLYCD):c.529-8C>T	rs3815806	0.06693
NM_012213.3(MLYCD):c.732G>A (p.Ser244=)	rs2278038	0.04474
NM_012213.3(MLYCD):c.444C>T (p.Asp148=)	rs62640904	0.03566
NM_012213.3(MLYCD):c.31A>G (p.Arg11Gly)	rs138107830	0.03048
NM_012213.3(MLYCD):c.850A>G (p.Thr284Ala)	rs62640903	0.02854
NM_012213.3(MLYCD):c.1464A>G (p.Gln488=)	rs1127368	0.00870
NM_012213.3(MLYCD):c.*618G>C	rs75701127	0.00812
NM_012213.3(MLYCD):c.-7G>A	rs9930103	0.00609
NM_012213.3(MLYCD):c.799-16C>T	rs150789545	0.00413
NM_012213.3(MLYCD):c.925A>C (p.Lys309Gln)	rs149926091	0.00324
NM_012213.3(MLYCD):c.206C>T (p.Ala69Val)	rs200579941	0.00284
NM_012213.3(MLYCD):c.776G>C (p.Gly259Ala)	rs77493891	0.00265
NM_012213.3(MLYCD):c.408C>G (p.Arg136=)	rs183593320	0.00108
NM_012213.3(MLYCD):c.375C>G (p.Ala125=)	rs375657338	0.00096
NM_012213.3(MLYCD):c.541G>A (p.Val181Met)	rs147617160	0.00061
NM_012213.3(MLYCD):c.232C>T (p.Leu78=)	rs541503395	0.00052
NM_012213.3(MLYCD):c.1098C>T (p.Ile366=)	rs199549095	0.00048
NM_012213.3(MLYCD):c.1074G>A (p.Ser358=)	rs377161125	0.00043
NM_012213.3(MLYCD):c.1328G>C (p.Gly443Ala)	rs200278015	0.00025
NM_012213.3(MLYCD):c.393C>T (p.Tyr131=)	rs560831102	0.00015
NM_012213.3(MLYCD):c.*254C>G	rs375604861	0.00009
NM_012213.3(MLYCD):c.1203G>A (p.Leu401=)	rs200341673	0.00004
NM_012213.3(MLYCD):c.*27C>T	rs565054759	0.00001
NM_012213.3(MLYCD):c.267C>T (p.Gly89=)	rs561775245	0.00001
NM_012213.3(MLYCD):c.*671C>T	rs74830340
NM_012213.3(MLYCD):c.1245G>A (p.Ala415=)
NM_012213.3(MLYCD):c.1368C>T (p.Tyr456=)

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