ClinVar Miner

List of variants in gene PCARE reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 95
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HGVS dbSNP
NM_001029883.3(PCARE):c.1038C>T (p.Cys346=)
NM_001029883.3(PCARE):c.1083G>A (p.Ser361=)
NM_001029883.3(PCARE):c.111A>G (p.Glu37=)
NM_001029883.3(PCARE):c.1137A>G (p.Glu379=) rs755968619
NM_001029883.3(PCARE):c.1219G>A (p.Gly407Ser)
NM_001029883.3(PCARE):c.1245A>T (p.Ser415=)
NM_001029883.3(PCARE):c.1293G>A (p.Arg431=)
NM_001029883.3(PCARE):c.1297C>T (p.Pro433Ser) rs200696965
NM_001029883.3(PCARE):c.1387G>A (p.Val463Ile)
NM_001029883.3(PCARE):c.156C>T (p.Asp52=)
NM_001029883.3(PCARE):c.1599G>A (p.Arg533=) rs781286343
NM_001029883.3(PCARE):c.159T>C (p.Ala53=)
NM_001029883.3(PCARE):c.1602C>T (p.Ser534=)
NM_001029883.3(PCARE):c.1719G>A (p.Val573=)
NM_001029883.3(PCARE):c.1725C>T (p.Pro575=)
NM_001029883.3(PCARE):c.1776G>A (p.Thr592=) rs201520631
NM_001029883.3(PCARE):c.1794G>A (p.Ser598=) rs535459255
NM_001029883.3(PCARE):c.1812G>A (p.Val604=)
NM_001029883.3(PCARE):c.1835T>C (p.Leu612Pro) rs200758183
NM_001029883.3(PCARE):c.1872G>A (p.Glu624=)
NM_001029883.3(PCARE):c.18A>T (p.Ser6=) rs1312286590
NM_001029883.3(PCARE):c.1941C>T (p.Ala647=) rs372588982
NM_001029883.3(PCARE):c.1944C>G (p.Ala648=)
NM_001029883.3(PCARE):c.1944C>T (p.Ala648=)
NM_001029883.3(PCARE):c.2034T>C (p.Pro678=)
NM_001029883.3(PCARE):c.2082C>T (p.Asp694=)
NM_001029883.3(PCARE):c.2121A>T (p.Pro707=)
NM_001029883.3(PCARE):c.2163T>C (p.Asn721=)
NM_001029883.3(PCARE):c.2191G>A (p.Val731Ile) rs201790782
NM_001029883.3(PCARE):c.2256C>T (p.Asp752=)
NM_001029883.3(PCARE):c.2259T>G (p.Ala753=)
NM_001029883.3(PCARE):c.2307C>T (p.Pro769=)
NM_001029883.3(PCARE):c.2346A>G (p.Gln782=) rs181545106
NM_001029883.3(PCARE):c.2348T>C (p.Ile783Thr) rs141559332
NM_001029883.3(PCARE):c.2442C>T (p.Ala814=)
NM_001029883.3(PCARE):c.2475G>A (p.Gly825=)
NM_001029883.3(PCARE):c.2496A>G (p.Pro832=) rs1572827287
NM_001029883.3(PCARE):c.2541G>A (p.Glu847=)
NM_001029883.3(PCARE):c.2595A>G (p.Pro865=)
NM_001029883.3(PCARE):c.2600C>T (p.Pro867Leu) rs182248363
NM_001029883.3(PCARE):c.2613C>G (p.Gly871=)
NM_001029883.3(PCARE):c.264T>C (p.Asp88=)
NM_001029883.3(PCARE):c.2691C>T (p.Thr897=)
NM_001029883.3(PCARE):c.2697C>T (p.Ser899=) rs1558488488
NM_001029883.3(PCARE):c.2727G>A (p.Gly909=)
NM_001029883.3(PCARE):c.2736G>A (p.Arg912=)
NM_001029883.3(PCARE):c.2766G>A (p.Leu922=) rs751605891
NM_001029883.3(PCARE):c.2811G>A (p.Lys937=)
NM_001029883.3(PCARE):c.2864G>A (p.Arg955Gln) rs184249075
NM_001029883.3(PCARE):c.2886C>T (p.His962=) rs759131866
NM_001029883.3(PCARE):c.2898A>C (p.Pro966=)
NM_001029883.3(PCARE):c.2911A>C (p.Arg971=)
NM_001029883.3(PCARE):c.294C>T (p.Thr98=)
NM_001029883.3(PCARE):c.2991G>A (p.Thr997=) rs528901190
NM_001029883.3(PCARE):c.3037C>G (p.Pro1013Ala)
NM_001029883.3(PCARE):c.30T>G (p.Leu10=) rs1297052773
NM_001029883.3(PCARE):c.3108C>T (p.Pro1036=)
NM_001029883.3(PCARE):c.3180C>A (p.Pro1060=)
NM_001029883.3(PCARE):c.3183C>G (p.Pro1061=)
NM_001029883.3(PCARE):c.3255G>A (p.Ser1085=)
NM_001029883.3(PCARE):c.3300G>A (p.Lys1100=)
NM_001029883.3(PCARE):c.3307A>G (p.Arg1103Gly)
NM_001029883.3(PCARE):c.3315T>C (p.Ser1105=)
NM_001029883.3(PCARE):c.3321C>T (p.Asp1107=)
NM_001029883.3(PCARE):c.3357A>C (p.Thr1119=)
NM_001029883.3(PCARE):c.3405G>A (p.Pro1135=)
NM_001029883.3(PCARE):c.3468C>T (p.Leu1156=)
NM_001029883.3(PCARE):c.3513G>A (p.Leu1171=)
NM_001029883.3(PCARE):c.3527A>G (p.Gln1176Arg) rs182812191
NM_001029883.3(PCARE):c.3609G>A (p.Pro1203=) rs375163820
NM_001029883.3(PCARE):c.3645T>C (p.Tyr1215=)
NM_001029883.3(PCARE):c.3651C>T (p.Ser1217=)
NM_001029883.3(PCARE):c.3666C>T (p.Asn1222=)
NM_001029883.3(PCARE):c.3684C>T (p.Ser1228=)
NM_001029883.3(PCARE):c.3705G>A (p.Pro1235=) rs191767954
NM_001029883.3(PCARE):c.3708G>A (p.Gly1236=)
NM_001029883.3(PCARE):c.3738C>T (p.Gly1246=)
NM_001029883.3(PCARE):c.3739G>A (p.Gly1247Ser) rs187333111
NM_001029883.3(PCARE):c.3783C>T (p.His1261=)
NM_001029883.3(PCARE):c.39C>T (p.Ser13=)
NM_001029883.3(PCARE):c.407A>G (p.Glu136Gly)
NM_001029883.3(PCARE):c.459G>A (p.Thr153=) rs372665350
NM_001029883.3(PCARE):c.462A>G (p.Ser154=)
NM_001029883.3(PCARE):c.530C>T (p.Pro177Leu) rs190791051
NM_001029883.3(PCARE):c.531G>A (p.Pro177=) rs200914951
NM_001029883.3(PCARE):c.624C>T (p.Ala208=)
NM_001029883.3(PCARE):c.645G>A (p.Leu215=) rs374663422
NM_001029883.3(PCARE):c.670C>T (p.Leu224=)
NM_001029883.3(PCARE):c.747G>A (p.Glu249=)
NM_001029883.3(PCARE):c.85C>T (p.Arg29Trp) rs201706430
NM_001029883.3(PCARE):c.867C>T (p.Thr289=) rs199729963
NM_001029883.3(PCARE):c.879G>T (p.Leu293=) rs201841912
NM_001029883.3(PCARE):c.961C>G (p.Leu321Val) rs147450324
NM_001029883.3(PCARE):c.963C>T (p.Leu321=)
NM_001029883.3(PCARE):c.996G>A (p.Ala332=) rs202025832

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