ClinVar Miner

List of variants in gene CLDN14 studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP
NC_000021.9:g.36460620A>G
NM_001146079.2(CLDN14):c.*107G>A rs112112443
NM_001146079.2(CLDN14):c.*10G>C rs139628442
NM_001146079.2(CLDN14):c.*222T>C
NM_001146079.2(CLDN14):c.*48G>A
NM_001146079.2(CLDN14):c.*51G>A rs114551506
NM_001146079.2(CLDN14):c.*66G>A
NM_001146079.2(CLDN14):c.-130G>A
NM_001146079.2(CLDN14):c.-136G>A rs886057053
NM_001146079.2(CLDN14):c.-187C>T rs886057054
NM_001146079.2(CLDN14):c.-242C>T rs78291168
NM_001146079.2(CLDN14):c.-264G>C rs188733
NM_001146079.2(CLDN14):c.-290A>G rs219742
NM_001146079.2(CLDN14):c.-297G>A rs140333712
NM_001146079.2(CLDN14):c.-337C>G rs117804848
NM_001146079.2(CLDN14):c.-390G>A rs150344346
NM_001146079.2(CLDN14):c.-426C>T
NM_001146079.2(CLDN14):c.-436G>A
NM_001146079.2(CLDN14):c.-445G>A
NM_001146079.2(CLDN14):c.-46G>A rs779699092
NM_001146079.2(CLDN14):c.-492C>T rs886057055
NM_001146079.2(CLDN14):c.-531G>A
NM_001146079.2(CLDN14):c.-54G>A rs886057051
NM_001146079.2(CLDN14):c.-5G>A
NM_001146079.2(CLDN14):c.-634G>A rs886057056
NM_001146079.2(CLDN14):c.-645G>T rs886057057
NM_001146079.2(CLDN14):c.-75G>T rs537529014
NM_001146079.2(CLDN14):c.-76C>T
NM_001146079.2(CLDN14):c.-82+2024G>A rs73902533
NM_001146079.2(CLDN14):c.-82+2044A>C
NM_001146079.2(CLDN14):c.-82+9G>C rs886057052
NM_001146079.2(CLDN14):c.11C>T (p.Thr4Met) rs113831133
NM_001146079.2(CLDN14):c.129C>T (p.Ala43=)
NM_001146079.2(CLDN14):c.167G>A (p.Trp56Ter) rs371100799
NM_001146079.2(CLDN14):c.169C>T (p.His57Tyr)
NM_001146079.2(CLDN14):c.18G>A (p.Val6=) rs387907417
NM_001146079.2(CLDN14):c.191G>A (p.Cys64Tyr) rs1568839335
NM_001146079.2(CLDN14):c.242G>A (p.Arg81His) rs368027306
NM_001146079.2(CLDN14):c.243C>T (p.Arg81=) rs219779
NM_001146079.2(CLDN14):c.254T>A (p.Val85Asp) rs74315437
NM_001146079.2(CLDN14):c.262T>C (p.Cys88Arg)
NM_001146079.2(CLDN14):c.295G>A (p.Val99Ile) rs371106978
NM_001146079.2(CLDN14):c.300C>T (p.Ile100=) rs113350364
NM_001146079.2(CLDN14):c.301G>A (p.Gly101Arg) rs74315438
NM_001146079.2(CLDN14):c.364G>A (p.Gly122Ser)
NM_001146079.2(CLDN14):c.369C>A (p.Thr123=) rs727502938
NM_001146079.2(CLDN14):c.378C>G (p.Ile126Met) rs886057049
NM_001146079.2(CLDN14):c.398del (p.Met133fs) rs786200885
NM_001146079.2(CLDN14):c.40_41insTGGTGCACGGCCGTGCA (p.Ser14fs)
NM_001146079.2(CLDN14):c.430G>A (p.Val144Met)
NM_001146079.2(CLDN14):c.450G>T (p.Pro150=) rs746102559
NM_001146079.2(CLDN14):c.488C>T (p.Ala163Val) rs143797113
NM_001146079.2(CLDN14):c.49G>A (p.Gly17Ser)
NM_001146079.2(CLDN14):c.513G>C (p.Ser171=)
NM_001146079.2(CLDN14):c.522G>A (p.Ser174=) rs763846537
NM_001146079.2(CLDN14):c.535A>G (p.Thr179Ala) rs759597838
NM_001146079.2(CLDN14):c.578C>T (p.Pro193Leu)
NM_001146079.2(CLDN14):c.587C>T (p.Ala196Val) rs200651246
NM_001146079.2(CLDN14):c.621C>T (p.Thr207=) rs139437157
NM_001146079.2(CLDN14):c.633C>T (p.Tyr211=) rs61745291
NM_001146079.2(CLDN14):c.63G>A (p.Thr21=) rs117560775
NM_001146079.2(CLDN14):c.681G>A (p.Ser227=)
NM_001146079.2(CLDN14):c.687G>A (p.Thr229=) rs219780
NM_001146079.2(CLDN14):c.690C>T (p.His230=) rs149733854
NM_001146079.2(CLDN14):c.694G>A (p.Gly232Arg) rs786204841
NM_001146079.2(CLDN14):c.89G>A (p.Trp30Ter)
NM_001146079.2(CLDN14):c.96G>C (p.Arg32Ser) rs886057050

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