ClinVar Miner

List of variants in gene PSTPIP1 reported as benign

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Gene type:
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Total variants: 79
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HGVS dbSNP
GRCh37/hg19 15q24.3(chr15:77328269-77332606)x0
NM_003978.5(PSTPIP1):c.*121C>T rs566906535
NM_003978.5(PSTPIP1):c.*156_*158del rs147238110
NM_003978.5(PSTPIP1):c.*38T>C rs201535027
NM_003978.5(PSTPIP1):c.*51G>A rs117378779
NM_003978.5(PSTPIP1):c.*93C>T rs554408944
NM_003978.5(PSTPIP1):c.-117C>T rs147120980
NM_003978.5(PSTPIP1):c.-124C>T rs760819203
NM_003978.5(PSTPIP1):c.-171A>T rs546291000
NM_003978.5(PSTPIP1):c.-421_-418CCTG[6] rs55909412
NM_003978.5(PSTPIP1):c.-421_-418CCTG[8] rs55909412
NM_003978.5(PSTPIP1):c.-436G>A rs548828496
NM_003978.5(PSTPIP1):c.1054G>A (p.Glu352Lys) rs201186216
NM_003978.5(PSTPIP1):c.1086G>A (p.Gln362=) rs528187669
NM_003978.5(PSTPIP1):c.1098G>A (p.Ala366=) rs35538044
NM_003978.5(PSTPIP1):c.1112C>T (p.Thr371Ile) rs34908107
NM_003978.5(PSTPIP1):c.1116G>A (p.Ala372=) rs369835681
NM_003978.5(PSTPIP1):c.1119+5G>C
NM_003978.5(PSTPIP1):c.1120-44_1120-31del rs201788590
NM_003978.5(PSTPIP1):c.1134G>A (p.Leu378=) rs529402949
NM_003978.5(PSTPIP1):c.1143C>T (p.Ser381=) rs141227274
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.1151A>G (p.Asp384Gly) rs200771233
NM_003978.5(PSTPIP1):c.1182T>C (p.Asp394=) rs199804922
NM_003978.5(PSTPIP1):c.1206C>T (p.Asn402=) rs146035424
NM_003978.5(PSTPIP1):c.1207G>C (p.Gly403Arg) rs369113632
NM_003978.5(PSTPIP1):c.1208G>A (p.Gly403Glu) rs201572812
NM_003978.5(PSTPIP1):c.1213C>T (p.Arg405Cys) rs201253322
NM_003978.5(PSTPIP1):c.1221C>A (p.Phe407Leu) rs200363654
NM_003978.5(PSTPIP1):c.1233C>T (p.Ser411=)
NM_003978.5(PSTPIP1):c.137+20del
NM_003978.5(PSTPIP1):c.137+28C>T rs79438763
NM_003978.5(PSTPIP1):c.137+47G>C rs3812911
NM_003978.5(PSTPIP1):c.137+57G>A rs3812912
NM_003978.5(PSTPIP1):c.147G>A (p.Ala49=) rs34618738
NM_003978.5(PSTPIP1):c.203C>T (p.Thr68Met) rs201872851
NM_003978.5(PSTPIP1):c.204G>A (p.Thr68=) rs113386299
NM_003978.5(PSTPIP1):c.212+12C>T rs3812914
NM_003978.5(PSTPIP1):c.236C>T (p.Ser79Phe) rs77026017
NM_003978.5(PSTPIP1):c.247+20G>A rs188931087
NM_003978.5(PSTPIP1):c.248-66G>A rs55775608
NM_003978.5(PSTPIP1):c.354+10G>A rs370745407
NM_003978.5(PSTPIP1):c.354+185C>T rs11636266
NM_003978.5(PSTPIP1):c.354+20C>T rs184279306
NM_003978.5(PSTPIP1):c.37T>G (p.Cys13Gly) rs376128040
NM_003978.5(PSTPIP1):c.417+207_417+208del rs3841234
NM_003978.5(PSTPIP1):c.417+232G>C rs3812915
NM_003978.5(PSTPIP1):c.418-20A>G rs545542379
NM_003978.5(PSTPIP1):c.418-6C>A rs200018722
NM_003978.5(PSTPIP1):c.516+160G>A rs80152051
NM_003978.5(PSTPIP1):c.516+177A>G rs56103874
NM_003978.5(PSTPIP1):c.543G>A (p.Lys181=) rs375950478
NM_003978.5(PSTPIP1):c.555C>T (p.Thr185=) rs370782742
NM_003978.5(PSTPIP1):c.563-82G>A rs10152353
NM_003978.5(PSTPIP1):c.563-8G>A rs183441330
NM_003978.5(PSTPIP1):c.586G>A (p.Ala196Thr) rs758911910
NM_003978.5(PSTPIP1):c.642+16G>A rs78282498
NM_003978.5(PSTPIP1):c.643-13C>A rs200459219
NM_003978.5(PSTPIP1):c.652C>T (p.Leu218=) rs35677716
NM_003978.5(PSTPIP1):c.657A>C (p.Gln219His) rs139362350
NM_003978.5(PSTPIP1):c.687C>T (p.Asn229=) rs542286074
NM_003978.5(PSTPIP1):c.741+273C>T rs79732372
NM_003978.5(PSTPIP1):c.747C>T (p.Tyr249=) rs557759616
NM_003978.5(PSTPIP1):c.773G>C (p.Gly258Ala) rs34240327
NM_003978.5(PSTPIP1):c.786C>T (p.Asp262=) rs35860563
NM_003978.5(PSTPIP1):c.799A>G (p.Ser267Gly) rs145239831
NM_003978.5(PSTPIP1):c.837C>T (p.Pro279=) rs149195362
NM_003978.5(PSTPIP1):c.838+145A>G rs4078354
NM_003978.5(PSTPIP1):c.838+40T>C rs77968440
NM_003978.5(PSTPIP1):c.838+45C>G
NM_003978.5(PSTPIP1):c.856A>G (p.Asn286Asp) rs377437961
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.915C>T (p.Cys305=) rs11858480
NM_003978.5(PSTPIP1):c.929+17C>T rs372335370
NM_003978.5(PSTPIP1):c.930-278T>C rs9806416
NM_003978.5(PSTPIP1):c.940C>T (p.Leu314=) rs201582038
NM_003978.5(PSTPIP1):c.985+6G>C rs139552419

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