ClinVar Miner

List of variants in gene PCARE reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_001029883.3(PCARE):c.102C>T (p.Gly34=) rs149915190
NM_001029883.3(PCARE):c.103G>A (p.Gly35Arg)
NM_001029883.3(PCARE):c.1215C>T (p.Gly405=) rs754808908
NM_001029883.3(PCARE):c.1262A>G (p.Lys421Arg) rs17007544
NM_001029883.3(PCARE):c.1387G>T (p.Val463Phe) rs199764925
NM_001029883.3(PCARE):c.1452C>T (p.Ser484=) rs13385188
NM_001029883.3(PCARE):c.1545A>G (p.Gln515=)
NM_001029883.3(PCARE):c.1582C>T (p.Arg528Cys) rs80151896
NM_001029883.3(PCARE):c.1739C>T (p.Thr580Met) rs10166913
NM_001029883.3(PCARE):c.1844T>A (p.Val615Asp) rs140776870
NM_001029883.3(PCARE):c.184C>G (p.Pro62Ala) rs76346220
NM_001029883.3(PCARE):c.1882G>A (p.Ala628Thr) rs571059484
NM_001029883.3(PCARE):c.1942G>A (p.Ala648Thr) rs75276619
NM_001029883.3(PCARE):c.2063G>A (p.Cys688Tyr) rs149601594
NM_001029883.3(PCARE):c.2112T>C (p.Asn704=) rs10200693
NM_001029883.3(PCARE):c.2374C>G (p.Leu792Val) rs17744093
NM_001029883.3(PCARE):c.2406A>G (p.Ala802=) rs375771666
NM_001029883.3(PCARE):c.2418C>T (p.Pro806=) rs189042259
NM_001029883.3(PCARE):c.2424G>A (p.Leu808=)
NM_001029883.3(PCARE):c.2499G>A (p.Pro833=) rs34253433
NM_001029883.3(PCARE):c.2502T>C (p.Pro834=) rs184644658
NM_001029883.3(PCARE):c.2539G>C (p.Glu847Gln)
NM_001029883.3(PCARE):c.258G>A (p.Arg86=) rs62132765
NM_001029883.3(PCARE):c.2601G>A (p.Pro867=)
NM_001029883.3(PCARE):c.2617A>G (p.Thr873Ala) rs190462758
NM_001029883.3(PCARE):c.2875G>A (p.Ala959Thr) rs192350796
NM_001029883.3(PCARE):c.2889C>T (p.Ser963=) rs144569618
NM_001029883.3(PCARE):c.2890G>A (p.Gly964Ser) rs371925633
NM_001029883.3(PCARE):c.2965C>G (p.Pro989Ala) rs184281410
NM_001029883.3(PCARE):c.3058C>A (p.Gln1020Lys) rs201355503
NM_001029883.3(PCARE):c.3058_3059delinsAG (p.Gln1020Arg) rs796065322
NM_001029883.3(PCARE):c.3059A>G (p.Gln1020Arg) rs200367963
NM_001029883.3(PCARE):c.3114G>C (p.Val1038=) rs140790266
NM_001029883.3(PCARE):c.3178C>A (p.Pro1060Thr) rs72861054
NM_001029883.3(PCARE):c.3264_3266del (p.Pro1089del) rs138020654
NM_001029883.3(PCARE):c.3291G>A (p.Gln1097=) rs183536545
NM_001029883.3(PCARE):c.3395A>C (p.Glu1132Ala) rs78874550
NM_001029883.3(PCARE):c.3447G>A (p.Pro1149=) rs200278694
NM_001029883.3(PCARE):c.3522C>T (p.Asp1174=) rs188815175
NM_001029883.3(PCARE):c.3525G>A (p.Ser1175=)
NM_001029883.3(PCARE):c.3626A>G (p.Asp1209Gly) rs572724183
NM_001029883.3(PCARE):c.3668+14T>C rs72861052
NM_001029883.3(PCARE):c.3669-2AGC[4]
NM_001029883.3(PCARE):c.366T>C (p.His122=) rs17007546
NM_001029883.3(PCARE):c.3739G>A (p.Gly1247Ser) rs187333111
NM_001029883.3(PCARE):c.3761C>T (p.Pro1254Leu) rs1975713
NM_001029883.3(PCARE):c.3780C>T (p.Gly1260=) rs572507416
NM_001029883.3(PCARE):c.3789G>A (p.Leu1263=) rs199689791
NM_001029883.3(PCARE):c.37A>T (p.Ser13Cys) rs10084168
NM_001029883.3(PCARE):c.3840G>A (p.Ala1280=) rs115730331
NM_001029883.3(PCARE):c.60G>A (p.Gln20=) rs35929540
NM_001029883.3(PCARE):c.679G>A (p.Glu227Lys) rs114057537
NM_001029883.3(PCARE):c.740T>C (p.Val247Ala) rs77828062
NM_001029883.3(PCARE):c.755C>A (p.Ala252Asp) rs77003681
NM_001029883.3(PCARE):c.773G>T (p.Arg258Ile) rs116156338
NM_001029883.3(PCARE):c.99G>A (p.Gln33=) rs146455733

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