ClinVar Miner

List of variants in gene CLRN1 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_001195794.1(CLRN1):c.-141C>T
NM_001195794.1(CLRN1):c.-186A>G
NM_001195794.1(CLRN1):c.-229A>G
NM_001195794.1(CLRN1):c.-274A>C rs886058092
NM_001195794.1(CLRN1):c.-289G>A rs55842922
NM_001195794.1(CLRN1):c.-82T>C rs778235601
NM_001195794.1(CLRN1):c.-91C>T
NM_174878.3(CLRN1):c.*1032T>C
NM_174878.3(CLRN1):c.*1038G>A rs201534956
NM_174878.3(CLRN1):c.*1039A>T rs200446881
NM_174878.3(CLRN1):c.*115G>A rs182501934
NM_174878.3(CLRN1):c.*1165C>G rs769315815
NM_174878.3(CLRN1):c.*1181T>C
NM_174878.3(CLRN1):c.*1262G>A
NM_174878.3(CLRN1):c.*1331C>T rs763746069
NM_174878.3(CLRN1):c.*249G>A
NM_174878.3(CLRN1):c.*265_*266AT[5] rs550716419
NM_174878.3(CLRN1):c.*275A>G rs570356810
NM_174878.3(CLRN1):c.*277_*278GT[11] rs34027634
NM_174878.3(CLRN1):c.*277_*278GT[12] rs34027634
NM_174878.3(CLRN1):c.*277_*278GT[15] rs34027634
NM_174878.3(CLRN1):c.*277_*278GT[16] rs34027634
NM_174878.3(CLRN1):c.*298T>C
NM_174878.3(CLRN1):c.*307G>T rs886058091
NM_174878.3(CLRN1):c.*425G>A rs778645950
NM_174878.3(CLRN1):c.*537T>C
NM_174878.3(CLRN1):c.*592G>C
NM_174878.3(CLRN1):c.*815T>C
NM_174878.3(CLRN1):c.*835G>T
NM_174878.3(CLRN1):c.*856G>A rs748935256
NM_174878.3(CLRN1):c.*90A>G rs780643561
NM_174878.3(CLRN1):c.*93T>C
NM_174878.3(CLRN1):c.*9C>G
NM_174878.3(CLRN1):c.118T>G (p.Cys40Gly) rs121908143
NM_174878.3(CLRN1):c.183G>A (p.Met61Ile) rs140094683
NM_174878.3(CLRN1):c.185A>G (p.Gln62Arg)
NM_174878.3(CLRN1):c.208G>T (p.Gly70Cys)
NM_174878.3(CLRN1):c.209G>A (p.Gly70Asp) rs1559996059
NM_174878.3(CLRN1):c.20A>T (p.Lys7Ile) rs3796241
NM_174878.3(CLRN1):c.218A>G (p.Gln73Arg) rs201008540
NM_174878.3(CLRN1):c.226T>C (p.Leu76=) rs139829306
NM_174878.3(CLRN1):c.254-2081G>A rs780023517
NM_174878.3(CLRN1):c.254-2099_254-2086del rs1553772861
NM_174878.3(CLRN1):c.254-2115del rs1032160668
NM_174878.3(CLRN1):c.254-2189dup rs1553772899
NM_174878.3(CLRN1):c.268C>G (p.Leu90Val)
NM_174878.3(CLRN1):c.291C>T (p.Ile97=) rs1231233910
NM_174878.3(CLRN1):c.322C>T (p.Leu108Phe)
NM_174878.3(CLRN1):c.380C>G (p.Pro127Arg)
NM_174878.3(CLRN1):c.406G>A (p.Gly136Arg)
NM_174878.3(CLRN1):c.407G>A (p.Gly136Glu) rs779258184
NM_174878.3(CLRN1):c.411G>A (p.Leu137=)
NM_174878.3(CLRN1):c.433+1061A>T rs567709615
NM_174878.3(CLRN1):c.433+1083ACCAGGC[3] rs768093614
NM_174878.3(CLRN1):c.433+10A>G
NM_174878.3(CLRN1):c.433+1102G>T rs1553772414
NM_174878.3(CLRN1):c.434-3C>A
NM_174878.3(CLRN1):c.456_458del (p.Met152del) rs1553770929
NM_174878.3(CLRN1):c.473A>G (p.Glu158Gly) rs369185342
NM_174878.3(CLRN1):c.502A>T (p.Ile168Phe)
NM_174878.3(CLRN1):c.529G>A (p.Val177Ile)
NM_174878.3(CLRN1):c.660C>T (p.Asp220=) rs148752352
NM_174878.3(CLRN1):c.66C>A (p.Leu22=)
NM_174878.3(CLRN1):c.92C>G (p.Pro31Arg)

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