ClinVar Miner

List of variants in gene PSTPIP1 reported as benign for not specified

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_003978.5(PSTPIP1):c.1116G>A (p.Ala372=) rs369835681
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.204G>A (p.Thr68=) rs113386299
NM_003978.5(PSTPIP1):c.212+12C>T rs3812914
NM_003978.5(PSTPIP1):c.247+20G>A rs188931087
NM_003978.5(PSTPIP1):c.354+10G>A rs370745407
NM_003978.5(PSTPIP1):c.354+20C>T rs184279306
NM_003978.5(PSTPIP1):c.418-20A>G rs545542379
NM_003978.5(PSTPIP1):c.563-8G>A rs183441330
NM_003978.5(PSTPIP1):c.642+16G>A rs78282498
NM_003978.5(PSTPIP1):c.643-13C>A rs200459219
NM_003978.5(PSTPIP1):c.657A>C (p.Gln219His) rs139362350
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.837C>T (p.Pro279=) rs149195362
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.985+6G>C rs139552419

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