ClinVar Miner

List of variants reported as uncertain significance for cataract 18 by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 116
Download table as spreadsheet
HGVS dbSNP
NM_024513.4(FYCO1):c.*1074C>T
NM_024513.4(FYCO1):c.*1149C>G rs886058561
NM_024513.4(FYCO1):c.*1185A>T rs538032998
NM_024513.4(FYCO1):c.*1211C>A
NM_024513.4(FYCO1):c.*1235C>A rs886058560
NM_024513.4(FYCO1):c.*1270T>C
NM_024513.4(FYCO1):c.*1285G>C rs780841652
NM_024513.4(FYCO1):c.*132C>T rs886058563
NM_024513.4(FYCO1):c.*1349T>C
NM_024513.4(FYCO1):c.*1398G>A
NM_024513.4(FYCO1):c.*1411G>A
NM_024513.4(FYCO1):c.*1445C>T rs143753654
NM_024513.4(FYCO1):c.*176C>T rs544729621
NM_024513.4(FYCO1):c.*2275G>A
NM_024513.4(FYCO1):c.*2286T>C rs886058557
NM_024513.4(FYCO1):c.*2301A>G rs886058556
NM_024513.4(FYCO1):c.*2307C>G rs886058555
NM_024513.4(FYCO1):c.*2343G>A
NM_024513.4(FYCO1):c.*2741G>A rs886058554
NM_024513.4(FYCO1):c.*2757C>A rs186073318
NM_024513.4(FYCO1):c.*2771A>G
NM_024513.4(FYCO1):c.*2889C>A rs886058553
NM_024513.4(FYCO1):c.*3006G>A
NM_024513.4(FYCO1):c.*3057G>A rs537667165
NM_024513.4(FYCO1):c.*3063G>A
NM_024513.4(FYCO1):c.*3191G>A rs886058552
NM_024513.4(FYCO1):c.*3278G>A
NM_024513.4(FYCO1):c.*3283G>A rs886058551
NM_024513.4(FYCO1):c.*3326G>A
NM_024513.4(FYCO1):c.*3366T>G rs886058550
NM_024513.4(FYCO1):c.*342C>T
NM_024513.4(FYCO1):c.*3502A>T rs753979161
NM_024513.4(FYCO1):c.*3512T>A
NM_024513.4(FYCO1):c.*3527G>A rs756372595
NM_024513.4(FYCO1):c.*3583C>T
NM_024513.4(FYCO1):c.*3691A>C
NM_024513.4(FYCO1):c.*431A>G
NM_024513.4(FYCO1):c.*59C>G
NM_024513.4(FYCO1):c.*620G>A rs886058562
NM_024513.4(FYCO1):c.*678A>G rs141954427
NM_024513.4(FYCO1):c.*709C>T rs559852330
NM_024513.4(FYCO1):c.*810G>A rs778420399
NM_024513.4(FYCO1):c.*988C>A
NM_024513.4(FYCO1):c.-214C>T rs576623682
NM_024513.4(FYCO1):c.107C>T (p.Thr36Met)
NM_024513.4(FYCO1):c.1098C>T (p.Ala366=) rs201904937
NM_024513.4(FYCO1):c.1121T>C (p.Met374Thr) rs139604029
NM_024513.4(FYCO1):c.1144G>A (p.Ala382Thr) rs886058570
NM_024513.4(FYCO1):c.1248G>A (p.Lys416=) rs149643762
NM_024513.4(FYCO1):c.1464A>T (p.Ala488=) rs886058569
NM_024513.4(FYCO1):c.150G>A (p.Glu50=) rs886058572
NM_024513.4(FYCO1):c.1549T>A (p.Phe517Ile) rs148594622
NM_024513.4(FYCO1):c.1628_1629del (p.Lys543fs) rs766571780
NM_024513.4(FYCO1):c.1651G>T (p.Gly551Cys)
NM_024513.4(FYCO1):c.1676C>T (p.Pro559Leu) rs759805930
NM_024513.4(FYCO1):c.1765G>A (p.Glu589Lys) rs886058568
NM_024513.4(FYCO1):c.1826G>T (p.Ser609Ile)
NM_024513.4(FYCO1):c.186C>T (p.Thr62=) rs147216026
NM_024513.4(FYCO1):c.1887C>T (p.Val629=) rs140372149
NM_024513.4(FYCO1):c.1933G>A (p.Asp645Asn) rs145238648
NM_024513.4(FYCO1):c.2037G>A (p.Ala679=) rs373400491
NM_024513.4(FYCO1):c.2121C>T (p.Gly707=)
NM_024513.4(FYCO1):c.2200G>C (p.Glu734Gln) rs750356269
NM_024513.4(FYCO1):c.2359C>T (p.Arg787Trp)
NM_024513.4(FYCO1):c.2389G>A (p.Ala797Thr)
NM_024513.4(FYCO1):c.2399G>A (p.Arg800Gln) rs773582689
NM_024513.4(FYCO1):c.2433C>G (p.Ser811Arg)
NM_024513.4(FYCO1):c.2455G>T (p.Val819Phe)
NM_024513.4(FYCO1):c.2507C>A (p.Ala836Asp)
NM_024513.4(FYCO1):c.2552G>A (p.Arg851His) rs145893350
NM_024513.4(FYCO1):c.2780C>T (p.Ala927Val)
NM_024513.4(FYCO1):c.2815G>C (p.Ala939Pro) rs531750827
NM_024513.4(FYCO1):c.2857G>T (p.Gly953Trp) rs150498691
NM_024513.4(FYCO1):c.2932C>G (p.Leu978Val) rs886058567
NM_024513.4(FYCO1):c.297A>T (p.Thr99=)
NM_024513.4(FYCO1):c.3024T>A (p.Ser1008Arg)
NM_024513.4(FYCO1):c.3047G>A (p.Ser1016Asn)
NM_024513.4(FYCO1):c.3151-12G>A
NM_024513.4(FYCO1):c.325C>T (p.Arg109Cys) rs886058571
NM_024513.4(FYCO1):c.3269+10A>T
NM_024513.4(FYCO1):c.337G>A (p.Val113Met)
NM_024513.4(FYCO1):c.3413A>G (p.Glu1138Gly) rs886058566
NM_024513.4(FYCO1):c.3433C>G (p.Leu1145Val)
NM_024513.4(FYCO1):c.3566T>C (p.Met1189Thr)
NM_024513.4(FYCO1):c.3587G>C (p.Arg1196Thr)
NM_024513.4(FYCO1):c.368A>C (p.Gln123Pro)
NM_024513.4(FYCO1):c.3809C>T (p.Thr1270Ile)
NM_024513.4(FYCO1):c.3825G>A (p.Pro1275=) rs748985200
NM_024513.4(FYCO1):c.3831C>T (p.Asp1277=)
NM_024513.4(FYCO1):c.3903A>G (p.Thr1301=) rs144525738
NM_024513.4(FYCO1):c.3920C>A (p.Ser1307Tyr)
NM_024513.4(FYCO1):c.3935C>T (p.Ala1312Val) rs140583635
NM_024513.4(FYCO1):c.3959C>A (p.Thr1320Asn)
NM_024513.4(FYCO1):c.3993C>T (p.Pro1331=) rs752606656
NM_024513.4(FYCO1):c.3999G>T (p.Gly1333=)
NM_024513.4(FYCO1):c.4042A>G (p.Ile1348Val) rs886058565
NM_024513.4(FYCO1):c.4078T>C (p.Phe1360Leu) rs886058564
NM_024513.4(FYCO1):c.4081G>A (p.Gly1361Arg)
NM_024513.4(FYCO1):c.4151C>G (p.Ala1384Gly)
NM_024513.4(FYCO1):c.4251+11G>A
NM_024513.4(FYCO1):c.4271G>A (p.Arg1424Gln) rs140159323
NM_024513.4(FYCO1):c.4321C>A (p.Pro1441Thr) rs185127002
NM_024513.4(FYCO1):c.4394C>T (p.Thr1465Met) rs201764993
NM_024513.4(FYCO1):c.443C>T (p.Ser148Leu)
NM_024513.4(FYCO1):c.452T>C (p.Val151Ala)
NM_024513.4(FYCO1):c.546G>A (p.Thr182=)
NM_024513.4(FYCO1):c.56-4A>G rs150959263
NM_024513.4(FYCO1):c.678C>T (p.Asn226=)
NM_024513.4(FYCO1):c.708A>G (p.Arg236=)
NM_024513.4(FYCO1):c.748C>T (p.Arg250Trp) rs142017802
NM_024513.4(FYCO1):c.793G>A (p.Ala265Thr)
NM_024513.4(FYCO1):c.833G>A (p.Arg278Lys) rs753095430
NM_024513.4(FYCO1):c.844C>G (p.Arg282Gly)
NM_024513.4(FYCO1):c.844C>T (p.Arg282Cys) rs201358723
NM_024513.4(FYCO1):c.868C>T (p.Arg290Cys) rs760164181
NM_024513.4(FYCO1):c.933T>C (p.Thr311=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.