List of variants reported as likely benign for cataract 38

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 95

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HGVS	dbSNP	gnomAD frequency
NM_018238.4(AGK):c.17A>G (p.Lys6Arg)	rs148294392	0.00226
NM_018238.4(AGK):c.*992G>A	rs191308473	0.00172
NM_018238.4(AGK):c.416C>G (p.Thr139Arg)	rs144706178	0.00166
NM_018238.4(AGK):c.29A>G (p.Asn10Ser)	rs35269563	0.00161
NM_018238.4(AGK):c.877+14C>T	rs41275003	0.00041
NM_018238.4(AGK):c.1131+11A>G	rs202069684	0.00038
NM_018238.4(AGK):c.*1467T>C	rs140297904	0.00022
NM_018238.4(AGK):c.727-9C>T	rs199977261	0.00017
NM_018238.4(AGK):c.222-13C>T	rs374601217	0.00013
NM_018238.4(AGK):c.26G>A (p.Arg9Gln)	rs577821330	0.00013
NM_018238.4(AGK):c.852G>A (p.Ala284=)	rs183816817	0.00013
NM_018238.4(AGK):c.519-5T>C	rs755469922	0.00007
NM_018238.4(AGK):c.327C>T (p.Leu109=)	rs148971840	0.00006
NM_018238.4(AGK):c.804C>T (p.Thr268=)	rs543549513	0.00006
NM_018238.4(AGK):c.976-20A>G	rs201192380	0.00006
NM_018238.4(AGK):c.621C>T (p.Thr207=)	rs140431258	0.00005
NM_018238.4(AGK):c.684G>A (p.Gly228=)	rs150732826	0.00005
NM_018238.4(AGK):c.101+7A>C	rs373899577	0.00004
NM_018238.4(AGK):c.142-11T>C	rs899737243	0.00004
NM_018238.4(AGK):c.221+9G>A	rs200123164	0.00003
NM_018238.4(AGK):c.589-20G>T	rs751876434	0.00003
NM_018238.4(AGK):c.243A>G (p.Glu81=)	rs745864268	0.00002
NM_018238.4(AGK):c.63G>C (p.Leu21=)	rs779484397	0.00002
NM_018238.4(AGK):c.*58G>A	rs562245960	0.00001
NM_018238.4(AGK):c.1197G>A (p.Leu399=)	rs139412235	0.00001
NM_018238.4(AGK):c.498C>T (p.Ala166=)	rs748557845	0.00001
NM_018238.4(AGK):c.101+13C>G
NM_018238.4(AGK):c.101+4_101+7dup
NM_018238.4(AGK):c.1046+11T>C
NM_018238.4(AGK):c.1046+7G>T
NM_018238.4(AGK):c.1047-12C>G
NM_018238.4(AGK):c.1047-7C>T
NM_018238.4(AGK):c.1047-8G>A
NM_018238.4(AGK):c.1068C>T (p.Pro356=)
NM_018238.4(AGK):c.1077C>T (p.His359=)
NM_018238.4(AGK):c.1089G>A (p.Thr363=)
NM_018238.4(AGK):c.1131+19G>A
NM_018238.4(AGK):c.1132-13C>A
NM_018238.4(AGK):c.1140G>A (p.Gly380=)
NM_018238.4(AGK):c.1176G>C (p.Ala392=)
NM_018238.4(AGK):c.1236G>A (p.Lys412=)
NM_018238.4(AGK):c.1260C>T (p.Pro420=)
NM_018238.4(AGK):c.1263C>A (p.Thr421=)	rs1166298575
NM_018238.4(AGK):c.141+16del
NM_018238.4(AGK):c.142-14C>G
NM_018238.4(AGK):c.142-18T>G
NM_018238.4(AGK):c.142-4T>C
NM_018238.4(AGK):c.142-8T>A
NM_018238.4(AGK):c.174A>G (p.Ala58=)
NM_018238.4(AGK):c.221+13G>A
NM_018238.4(AGK):c.222-20A>G
NM_018238.4(AGK):c.237A>G (p.Leu79=)
NM_018238.4(AGK):c.267T>C (p.His89=)
NM_018238.4(AGK):c.298-18G>A
NM_018238.4(AGK):c.298-18G>C
NM_018238.4(AGK):c.298-18G>T
NM_018238.4(AGK):c.391-13A>G	rs752545115
NM_018238.4(AGK):c.391-6T>C
NM_018238.4(AGK):c.396T>C (p.Val132=)
NM_018238.4(AGK):c.411A>T (p.Arg137=)
NM_018238.4(AGK):c.423+19T>C
NM_018238.4(AGK):c.424-14C>T
NM_018238.4(AGK):c.424-4C>T
NM_018238.4(AGK):c.424-5C>A	rs113599212
NM_018238.4(AGK):c.424-5C>G	rs113599212
NM_018238.4(AGK):c.424-5C>T	rs113599212
NM_018238.4(AGK):c.424-6C>T
NM_018238.4(AGK):c.424-8C>G
NM_018238.4(AGK):c.462G>A (p.Leu154=)
NM_018238.4(AGK):c.492C>G (p.Leu164=)	rs1485021759
NM_018238.4(AGK):c.495T>C (p.Phe165=)
NM_018238.4(AGK):c.519-19A>G
NM_018238.4(AGK):c.519-4_519-3del	rs770005760
NM_018238.4(AGK):c.573T>C (p.Asp191=)
NM_018238.4(AGK):c.579G>A (p.Leu193=)	rs745967065
NM_018238.4(AGK):c.621C>G (p.Thr207=)
NM_018238.4(AGK):c.654C>A (p.Gly218=)
NM_018238.4(AGK):c.654C>T (p.Gly218=)
NM_018238.4(AGK):c.668+9T>C
NM_018238.4(AGK):c.669-16C>A
NM_018238.4(AGK):c.717C>T (p.Ser239=)
NM_018238.4(AGK):c.726+18T>G
NM_018238.4(AGK):c.726+9G>T
NM_018238.4(AGK):c.819T>C (p.Pro273=)
NM_018238.4(AGK):c.877+13G>A
NM_018238.4(AGK):c.877+19A>G
NM_018238.4(AGK):c.878-15A>T
NM_018238.4(AGK):c.878-17C>T
NM_018238.4(AGK):c.878-6C>T	rs2117014175
NM_018238.4(AGK):c.900G>A (p.Pro300=)
NM_018238.4(AGK):c.924G>A (p.Leu308=)
NM_018238.4(AGK):c.954G>A (p.Arg318=)
NM_018238.4(AGK):c.963G>A (p.Gln321=)	rs746403177
NM_018238.4(AGK):c.972G>A (p.Pro324=)
NM_018238.4(AGK):c.976-9C>T	rs746375297

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