ClinVar Miner

List of variants in gene PSTPIP1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 118
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HGVS dbSNP
NM_003978.5(PSTPIP1):c.-123G>A
NM_003978.5(PSTPIP1):c.-124C>T rs760819203
NM_003978.5(PSTPIP1):c.-16C>T rs372407300
NM_003978.5(PSTPIP1):c.1014C>T (p.Pro338=) rs368838637
NM_003978.5(PSTPIP1):c.1018C>T (p.Arg340Trp)
NM_003978.5(PSTPIP1):c.1032C>T (p.Val344=)
NM_003978.5(PSTPIP1):c.1044C>T (p.Ile348=)
NM_003978.5(PSTPIP1):c.1054G>A (p.Glu352Lys) rs201186216
NM_003978.5(PSTPIP1):c.1074C>T (p.Ala358=)
NM_003978.5(PSTPIP1):c.1098G>A (p.Ala366=) rs35538044
NM_003978.5(PSTPIP1):c.1104C>T (p.Tyr368=)
NM_003978.5(PSTPIP1):c.1112C>T (p.Thr371Ile) rs34908107
NM_003978.5(PSTPIP1):c.1119+3_1119+6dup rs1596141513
NM_003978.5(PSTPIP1):c.1138C>T (p.Leu380=)
NM_003978.5(PSTPIP1):c.1144G>A (p.Ala382Thr) rs145344175
NM_003978.5(PSTPIP1):c.1145C>T (p.Ala382Val) rs202205180
NM_003978.5(PSTPIP1):c.1146G>A (p.Ala382=) rs760234757
NM_003978.5(PSTPIP1):c.1151A>G (p.Asp384Gly) rs200771233
NM_003978.5(PSTPIP1):c.1158G>A (p.Leu386=) rs752462668
NM_003978.5(PSTPIP1):c.1176G>A (p.Gly392=) rs181929438
NM_003978.5(PSTPIP1):c.1179G>A (p.Glu393=)
NM_003978.5(PSTPIP1):c.1182T>C (p.Asp394=) rs199804922
NM_003978.5(PSTPIP1):c.1213C>T (p.Arg405Cys) rs201253322
NM_003978.5(PSTPIP1):c.1215T>A (p.Arg405=) rs887633148
NM_003978.5(PSTPIP1):c.1221C>A (p.Phe407Leu) rs200363654
NM_003978.5(PSTPIP1):c.1221C>T (p.Phe407=) rs200363654
NM_003978.5(PSTPIP1):c.123G>A (p.Glu41=) rs766141606
NM_003978.5(PSTPIP1):c.1242G>A (p.Glu414=) rs1158206044
NM_003978.5(PSTPIP1):c.1248T>C (p.Leu416=) rs556322755
NM_003978.5(PSTPIP1):c.138-5dup rs755268431
NM_003978.5(PSTPIP1):c.138-6T>C rs765550656
NM_003978.5(PSTPIP1):c.138-8T>C rs1057523945
NM_003978.5(PSTPIP1):c.147G>A (p.Ala49=) rs34618738
NM_003978.5(PSTPIP1):c.159C>T (p.Tyr53=) rs563906441
NM_003978.5(PSTPIP1):c.203C>T (p.Thr68Met) rs201872851
NM_003978.5(PSTPIP1):c.212+248T>C rs112070036
NM_003978.5(PSTPIP1):c.222G>A (p.Arg74=) rs1435290161
NM_003978.5(PSTPIP1):c.236C>T (p.Ser79Phe) rs77026017
NM_003978.5(PSTPIP1):c.248-5C>T rs1266014755
NM_003978.5(PSTPIP1):c.255G>A (p.Glu85=)
NM_003978.5(PSTPIP1):c.304C>T (p.Leu102=) rs1401702747
NM_003978.5(PSTPIP1):c.354+10G>A rs370745407
NM_003978.5(PSTPIP1):c.354+20C>A
NM_003978.5(PSTPIP1):c.355-16C>G rs767272289
NM_003978.5(PSTPIP1):c.355-17C>T rs886038536
NM_003978.5(PSTPIP1):c.36+147G>T rs112875317
NM_003978.5(PSTPIP1):c.36+15T>C rs752123803
NM_003978.5(PSTPIP1):c.363C>T (p.Ala121=)
NM_003978.5(PSTPIP1):c.37-200A>C rs113013219
NM_003978.5(PSTPIP1):c.37-5C>T rs879254119
NM_003978.5(PSTPIP1):c.384G>A (p.Lys128=) rs868533109
NM_003978.5(PSTPIP1):c.417+156C>T rs113421352
NM_003978.5(PSTPIP1):c.417+176G>T rs148152818
NM_003978.5(PSTPIP1):c.417+7G>A
NM_003978.5(PSTPIP1):c.418-18G>A rs1281406107
NM_003978.5(PSTPIP1):c.418-20A>G rs545542379
NM_003978.5(PSTPIP1):c.418-5C>T
NM_003978.5(PSTPIP1):c.418-9C>A
NM_003978.5(PSTPIP1):c.426G>A (p.Lys142=)
NM_003978.5(PSTPIP1):c.432C>T (p.Tyr144=)
NM_003978.5(PSTPIP1):c.488C>T (p.Ala163Val) rs774530073
NM_003978.5(PSTPIP1):c.516+3G>A
NM_003978.5(PSTPIP1):c.517-149G>T rs115670384
NM_003978.5(PSTPIP1):c.517-4T>C
NM_003978.5(PSTPIP1):c.531C>T (p.Ala177=)
NM_003978.5(PSTPIP1):c.549G>A (p.Ser183=)
NM_003978.5(PSTPIP1):c.555C>T (p.Thr185=) rs370782742
NM_003978.5(PSTPIP1):c.558G>A (p.Glu186=) rs879254120
NM_003978.5(PSTPIP1):c.563-252A>G rs112105697
NM_003978.5(PSTPIP1):c.563-9C>T rs768152191
NM_003978.5(PSTPIP1):c.564G>A (p.Glu188=) rs879253893
NM_003978.5(PSTPIP1):c.575G>A (p.Arg192Lys)
NM_003978.5(PSTPIP1):c.59C>T (p.Thr20Met) rs553718554
NM_003978.5(PSTPIP1):c.5T>C (p.Met2Thr) rs541085532
NM_003978.5(PSTPIP1):c.60G>C (p.Thr20=)
NM_003978.5(PSTPIP1):c.621G>A (p.Gln207=)
NM_003978.5(PSTPIP1):c.629G>A (p.Arg210Gln) rs776576205
NM_003978.5(PSTPIP1):c.642+64C>T rs79985146
NM_003978.5(PSTPIP1):c.643-128T>C rs114248616
NM_003978.5(PSTPIP1):c.643-13C>A rs200459219
NM_003978.5(PSTPIP1):c.657A>C (p.Gln219His) rs139362350
NM_003978.5(PSTPIP1):c.657A>G (p.Gln219=) rs139362350
NM_003978.5(PSTPIP1):c.66C>T (p.Tyr22=)
NM_003978.5(PSTPIP1):c.675C>A (p.Thr225=)
NM_003978.5(PSTPIP1):c.675C>T (p.Thr225=) rs770958110
NM_003978.5(PSTPIP1):c.687C>T (p.Asn229=) rs542286074
NM_003978.5(PSTPIP1):c.693G>A (p.Leu231=) rs374055726
NM_003978.5(PSTPIP1):c.747C>T (p.Tyr249=) rs557759616
NM_003978.5(PSTPIP1):c.774C>G (p.Gly258=)
NM_003978.5(PSTPIP1):c.786C>T (p.Asp262=) rs35860563
NM_003978.5(PSTPIP1):c.789C>T (p.Ala263=)
NM_003978.5(PSTPIP1):c.792C>T (p.Asp264=) rs1224633016
NM_003978.5(PSTPIP1):c.795C>T (p.Ile265=) rs368528834
NM_003978.5(PSTPIP1):c.796G>A (p.Asp266Asn) rs104895418
NM_003978.5(PSTPIP1):c.813C>T (p.Ala271=) rs1596127197
NM_003978.5(PSTPIP1):c.822G>A (p.Thr274=)
NM_003978.5(PSTPIP1):c.837C>G (p.Pro279=) rs149195362
NM_003978.5(PSTPIP1):c.838+10G>A rs747042572
NM_003978.5(PSTPIP1):c.838+16C>T
NM_003978.5(PSTPIP1):c.838+17G>C rs371715620
NM_003978.5(PSTPIP1):c.838+31C>G rs545108125
NM_003978.5(PSTPIP1):c.838+82G>A rs56266471
NM_003978.5(PSTPIP1):c.838+9C>T rs778120164
NM_003978.5(PSTPIP1):c.839-12dup rs759640462
NM_003978.5(PSTPIP1):c.839-4G>A rs1367241638
NM_003978.5(PSTPIP1):c.846G>A (p.Val282=) rs1596129223
NM_003978.5(PSTPIP1):c.852C>T (p.Tyr284=)
NM_003978.5(PSTPIP1):c.856A>G (p.Asn286Asp) rs377437961
NM_003978.5(PSTPIP1):c.864C>T (p.Tyr288=) rs763986763
NM_003978.5(PSTPIP1):c.882G>A (p.Pro294=) rs200796501
NM_003978.5(PSTPIP1):c.908C>T (p.Pro303Leu) rs189773500
NM_003978.5(PSTPIP1):c.912C>A (p.Ser304=) rs1181224630
NM_003978.5(PSTPIP1):c.929+18G>A rs773172907
NM_003978.5(PSTPIP1):c.929+9C>G rs1284155822
NM_003978.5(PSTPIP1):c.948C>T (p.His316=) rs1386946850
NM_003978.5(PSTPIP1):c.957C>G (p.Pro319=)
NM_003978.5(PSTPIP1):c.985+19G>T rs192912170
NM_003978.5(PSTPIP1):c.987G>A (p.Ala329=)

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