ClinVar Miner

List of variants in gene CLDN19 reported as uncertain significance for perceptual disorders

Included ClinVar conditions (765):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_148960.3(CLDN19):c.*735G>C rs142957479 0.00490
NM_148960.3(CLDN19):c.*1357C>T rs200527665 0.00216
NM_148960.3(CLDN19):c.*1073G>A rs1057515527 0.00121
NM_148960.3(CLDN19):c.*1428A>G rs149256970 0.00111
NM_148960.3(CLDN19):c.65T>C (p.Ile22Thr) rs140913043 0.00056
NM_148960.3(CLDN19):c.*547C>T rs549719300 0.00054
NM_148960.3(CLDN19):c.646G>A (p.Ala216Thr) rs147528059 0.00046
NM_148960.3(CLDN19):c.-146G>A rs144607541 0.00032
NM_148960.3(CLDN19):c.*639C>T rs1030310070 0.00021
NM_148960.3(CLDN19):c.*523G>A rs776804215 0.00020
NM_148960.3(CLDN19):c.*45G>A rs200471599 0.00015
NM_148960.3(CLDN19):c.498C>T (p.Phe166=) rs776225389 0.00013
NM_148960.3(CLDN19):c.*257C>T rs796637327 0.00010
NM_148960.3(CLDN19):c.*1072C>T rs887547668 0.00009
NM_148960.3(CLDN19):c.*1353G>A rs745884385 0.00009
NM_148960.3(CLDN19):c.*800C>T rs777568849 0.00009
NM_148960.3(CLDN19):c.*1909G>A rs909291003 0.00007
NM_148960.3(CLDN19):c.*867C>G rs796839004 0.00006
NM_148960.3(CLDN19):c.168C>G (p.Ser56=) rs907045006 0.00006
NM_148960.3(CLDN19):c.560C>T (p.Pro187Leu) rs531931336 0.00005
NM_148960.3(CLDN19):c.*19G>A rs777408812 0.00004
NM_148960.3(CLDN19):c.*285C>A rs897677267 0.00004
NM_148960.3(CLDN19):c.*624C>T rs761260010 0.00004
NM_148960.3(CLDN19):c.206C>T (p.Ser69Leu) rs373645751 0.00004
NM_148960.3(CLDN19):c.314C>T (p.Thr105Met) rs200640147 0.00004
NM_148960.3(CLDN19):c.349C>T (p.Arg117Cys) rs765527366 0.00004
NM_148960.3(CLDN19):c.579C>G (p.Asn193Lys) rs758094656 0.00004
NM_148960.3(CLDN19):c.658G>T (p.Gly220Cys) rs200491942 0.00004
NM_148960.3(CLDN19):c.526G>A (p.Val176Met) rs772247940 0.00003
NM_148960.3(CLDN19):c.337A>G (p.Ile113Val) rs755364712 0.00002
NM_148960.3(CLDN19):c.*1008C>T rs1482159495 0.00001
NM_148960.3(CLDN19):c.*119C>T rs376052803 0.00001
NM_148960.3(CLDN19):c.*1483G>T rs1051069098 0.00001
NM_148960.3(CLDN19):c.*1698A>G rs765727450 0.00001
NM_148960.3(CLDN19):c.*177C>A rs371735000 0.00001
NM_148960.3(CLDN19):c.*1822C>T rs1651242713 0.00001
NM_148960.3(CLDN19):c.*1829A>G rs987445393 0.00001
NM_148960.3(CLDN19):c.140A>G (p.Tyr47Cys) rs1291749652 0.00001
NM_148960.3(CLDN19):c.153G>T (p.Trp51Cys) rs387907418 0.00001
NM_148960.3(CLDN19):c.335C>T (p.Pro112Leu) rs867064302 0.00001
NM_148960.3(CLDN19):c.350G>A (p.Arg117His) rs377319583 0.00001
NM_148960.3(CLDN19):c.622C>T (p.Arg208Ter) rs1011136678 0.00001
NM_148960.3(CLDN19):c.652G>A (p.Ala218Thr) rs535667246 0.00001
NM_148960.3(CLDN19):c.671T>A (p.Val224Glu) rs387907420 0.00001
NM_148960.3(CLDN19):c.*1172C>T rs796988312
NM_148960.3(CLDN19):c.*1312G>A rs972101560
NM_148960.3(CLDN19):c.*1312G>T rs972101560
NM_148960.3(CLDN19):c.*1336T>C rs1651260597
NM_148960.3(CLDN19):c.*1621T>C rs1057515454
NM_148960.3(CLDN19):c.*1772A>C rs1570440246
NM_148960.3(CLDN19):c.*1908C>T rs1178386071
NM_148960.3(CLDN19):c.*1919G>A rs1201425315
NM_148960.3(CLDN19):c.*1925T>C rs1436636389
NM_148960.3(CLDN19):c.*1965T>G rs1224371085
NM_148960.3(CLDN19):c.*491C>T rs762244030
NM_148960.3(CLDN19):c.*598G>T rs1651290159
NM_148960.3(CLDN19):c.*642G>A rs781380872
NM_148960.3(CLDN19):c.-145C>T rs1057515569
NM_148960.3(CLDN19):c.-150C>T rs941943594
NM_148960.3(CLDN19):c.-24_47dup (p.Gly17fs)
NM_148960.3(CLDN19):c.106G>T (p.Ala36Ser)
NM_148960.3(CLDN19):c.124A>G (p.Thr42Ala)
NM_148960.3(CLDN19):c.148C>A (p.Leu50Ile)
NM_148960.3(CLDN19):c.148C>T (p.Leu50Phe)
NM_148960.3(CLDN19):c.163G>A (p.Ala55Thr)
NM_148960.3(CLDN19):c.173G>T (p.Ser58Ile)
NM_148960.3(CLDN19):c.277G>C (p.Val93Leu)
NM_148960.3(CLDN19):c.317G>A (p.Arg106Gln)
NM_148960.3(CLDN19):c.31T>C (p.Tyr11His)
NM_148960.3(CLDN19):c.385G>C (p.Ala129Pro)
NM_148960.3(CLDN19):c.402G>C (p.Leu134Phe)
NM_148960.3(CLDN19):c.429G>T (p.Leu143=)
NM_148960.3(CLDN19):c.439G>A (p.Glu147Lys) rs1651434032
NM_148960.3(CLDN19):c.455G>A (p.Ser152Asn)
NM_148960.3(CLDN19):c.473+1G>T
NM_148960.3(CLDN19):c.503G>T (p.Gly168Val)
NM_148960.3(CLDN19):c.526G>T (p.Val176Leu)
NM_148960.3(CLDN19):c.617C>T (p.Ala206Val)
NM_148960.3(CLDN19):c.626+5G>A
NM_148960.3(CLDN19):c.626+7C>A
NM_148960.3(CLDN19):c.626A>G (p.Glu209Gly)
NM_148960.3(CLDN19):c.659G>T (p.Gly220Val)

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.