ClinVar Miner

List of variants in gene PSTPIP1 reported as likely benign by Invitae

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Total variants: 64
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HGVS dbSNP
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.1104C>T (p.Tyr368=)
NM_003978.5(PSTPIP1):c.1119+3_1119+6dup rs1596141513
NM_003978.5(PSTPIP1):c.1138C>T (p.Leu380=)
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.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>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.159C>T (p.Tyr53=) rs563906441
NM_003978.5(PSTPIP1):c.222G>A (p.Arg74=) rs1435290161
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.363C>T (p.Ala121=)
NM_003978.5(PSTPIP1):c.384G>A (p.Lys128=) rs868533109
NM_003978.5(PSTPIP1):c.417+7G>A
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.516+3G>A
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.563-9C>T rs768152191
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.643-13C>A rs200459219
NM_003978.5(PSTPIP1):c.66C>T (p.Tyr22=)
NM_003978.5(PSTPIP1):c.675C>A (p.Thr225=)
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.789C>T (p.Ala263=)
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.822G>A (p.Thr274=)
NM_003978.5(PSTPIP1):c.838+10G>A rs747042572
NM_003978.5(PSTPIP1):c.838+9C>T rs778120164
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.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.987G>A (p.Ala329=)

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