List of variants in gene PCARE reported as likely benign for perceptual disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 41

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HGVS	dbSNP	gnomAD frequency
NM_001029883.3(PCARE):c.*1704A>G	rs72788189	0.04109
NM_001029883.3(PCARE):c.*3041A>G	rs17007522	0.02184
NM_001029883.3(PCARE):c.*1601G>A	rs72861029	0.02029
NM_001029883.3(PCARE):c.*983G>A	rs74315958	0.01979
NM_001029883.3(PCARE):c.*2584C>T	rs79961309	0.01867
NM_001029883.3(PCARE):c.*2293G>C	rs1562394	0.01852
NM_001029883.3(PCARE):c.*2300C>T	rs115478100	0.01474
NM_001029883.3(PCARE):c.1844T>A (p.Val615Asp)	rs140776870	0.01391
NM_001029883.3(PCARE):c.*1748C>T	rs114193888	0.01296
NM_001029883.3(PCARE):c.*286G>T	rs78759931	0.01291
NM_001029883.3(PCARE):c.*2209G>A	rs77448535	0.01239
NM_001029883.3(PCARE):c.366T>C (p.His122=)	rs17007546	0.01047
NM_001029883.3(PCARE):c.*686A>T	rs116550481	0.00990
NM_001029883.3(PCARE):c.*1742G>C	rs138102302	0.00848
NM_001029883.3(PCARE):c.*1145G>A	rs115327633	0.00846
NM_001029883.3(PCARE):c.*778A>T	rs114774220	0.00686
NM_001029883.3(PCARE):c.3447G>A (p.Pro1149=)	rs200278694	0.00371
NM_001029883.3(PCARE):c.3739G>A (p.Gly1247Ser)	rs187333111	0.00365
NM_001029883.3(PCARE):c.3522C>T (p.Asp1174=)	rs188815175	0.00296
NM_001029883.3(PCARE):c.2600C>T (p.Pro867Leu)	rs182248363	0.00192
NM_001029883.3(PCARE):c.2864G>A (p.Arg955Gln)	rs184249075	0.00126
NM_001029883.3(PCARE):c.1582C>T (p.Arg528Cys)	rs80151896	0.00051
NM_001029883.3(PCARE):c.3704C>T (p.Pro1235Leu)	rs201933656	0.00033
NM_001029883.3(PCARE):c.959G>A (p.Arg320His)	rs201617661	0.00029
NM_001029883.3(PCARE):c.531G>A (p.Pro177=)	rs200914951	0.00016
NM_001029883.3(PCARE):c.3527A>G (p.Gln1176Arg)	rs182812191	0.00013
NM_001029883.3(PCARE):c.2803G>A (p.Glu935Lys)	rs200817926	0.00009
NM_001029883.3(PCARE):c.635G>A (p.Arg212Gln)	rs763441352	0.00008
NM_001029883.3(PCARE):c.1775C>T (p.Thr592Met)	rs202166083	0.00006
NM_001029883.3(PCARE):c.2898A>C (p.Pro966=)	rs187119693	0.00005
NM_001029883.3(PCARE):c.3531G>A (p.Arg1177=)	rs189904739	0.00004
NM_001029883.3(PCARE):c.3404C>T (p.Pro1135Leu)	rs756152942	0.00002
NM_001029883.3(PCARE):c.358G>C (p.Gly120Arg)	rs140625913	0.00002
NM_001029883.3(PCARE):c.407A>G (p.Glu136Gly)	rs761117759	0.00002
NM_001029883.3(PCARE):c.1137A>G (p.Glu379=)	rs755968619	0.00001
NM_001029883.3(PCARE):c.1944C>T (p.Ala648=)	rs746635522
NM_001029883.3(PCARE):c.2530G>A (p.Ala844Thr)	rs370203821
NM_001029883.3(PCARE):c.2965C>G (p.Pro989Ala)	rs184281410
NM_001029883.3(PCARE):c.3058_3059delinsAG (p.Gln1020Arg)	rs796065322
NM_001029883.3(PCARE):c.3469G>A (p.Gly1157Arg)	rs755486918
NM_001029883.3(PCARE):c.3722C>T (p.Ser1241Phe)	rs78471512

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