List of variants in gene MCCC1 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_020166.5(MCCC1):c.1595-181T>C	rs112734059	0.02246
NM_020166.5(MCCC1):c.1268-90C>T	rs140957052	0.01716
NM_020166.5(MCCC1):c.273+270C>T	rs74380421	0.01279
NM_020166.5(MCCC1):c.1614G>A (p.Ser538=)	rs34749281	0.01175
NM_020166.5(MCCC1):c.2049+31G>A	rs73068824	0.01038
NM_020166.5(MCCC1):c.1083+208C>G	rs113456152	0.00999
NM_020166.5(MCCC1):c.1595-111A>G	rs112025174	0.00864
NM_020166.5(MCCC1):c.1595-96C>T	rs12330492	0.00827
NM_020166.5(MCCC1):c.874-95A>G	rs144420749	0.00788
NM_020166.5(MCCC1):c.1595-180A>G	rs193164116	0.00778
NM_020166.5(MCCC1):c.1499G>A (p.Arg500Gln)	rs78726268	0.00748
NM_020166.5(MCCC1):c.1594+127G>T	rs143318455	0.00744
NM_020166.5(MCCC1):c.873+36G>A	rs114706421	0.00527
NM_020166.5(MCCC1):c.273+69A>G	rs150193548	0.00505
NM_020166.5(MCCC1):c.1682-75G>T	rs73068830	0.00487
NM_020166.5(MCCC1):c.726T>C (p.Asp242=)	rs36206712	0.00445
NM_020166.5(MCCC1):c.2049+237T>C	rs537365135	0.00418
NM_020166.5(MCCC1):c.*1A>T	rs115605600	0.00230
NM_020166.5(MCCC1):c.1337C>T (p.Ala446Val)	rs144182725	0.00068
NM_020166.5(MCCC1):c.1268-89G>A	rs73068841	0.00049
NM_020166.5(MCCC1):c.267A>C (p.Val89=)	rs369138447	0.00036
NM_020166.5(MCCC1):c.2034C>T (p.Ile678=)	rs150305281	0.00032
NM_020166.5(MCCC1):c.294C>T (p.Ile98=)	rs368288499	0.00007
NM_020166.5(MCCC1):c.2010G>A (p.Ala670=)	rs370727510	0.00003
NM_020166.5(MCCC1):c.1083+320del	rs35283773
NM_020166.5(MCCC1):c.156C>A (p.Val52=)	rs398124353
NM_020166.5(MCCC1):c.1681+92_1681+100dup	rs146243904
NM_020166.5(MCCC1):c.1851T>C (p.Thr617=)	rs1577239619
NM_020166.5(MCCC1):c.192G>A (p.Val64=)	rs1360164882
NM_020166.5(MCCC1):c.231G>A (p.Ala77=)	rs144230304
NM_020166.5(MCCC1):c.492-92T>A	rs112348183
NM_020166.5(MCCC1):c.54G>A (p.Arg18=)	rs1577376491
NM_020166.5(MCCC1):c.874-6del	rs755494348

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