ClinVar Miner

List of variants in gene PTPN11 reported as likely benign for Cardiovascular phenotype

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_002834.5(PTPN11):c.1658C>T (p.Thr553Met) rs148176616 0.00048
NM_002834.5(PTPN11):c.1379+20C>T rs184743462 0.00047
NM_002834.5(PTPN11):c.48A>G (p.Ala16=) rs372736227 0.00029
NM_002834.5(PTPN11):c.333-3T>C rs146749153 0.00026
NM_002834.5(PTPN11):c.925A>G (p.Ile309Val) rs201787206 0.00026
NM_002834.5(PTPN11):c.1746C>T (p.Asn582=) rs397516800 0.00013
NM_002834.5(PTPN11):c.558G>T (p.Arg186=) rs200920312 0.00011
NM_002834.5(PTPN11):c.1449T>G (p.Gly483=) rs143238917 0.00009
NM_002834.5(PTPN11):c.486C>T (p.Asp162=) rs397507522 0.00009
NM_002834.5(PTPN11):c.1362G>A (p.Pro454=) rs771967829 0.00008
NM_002834.5(PTPN11):c.1740T>C (p.Tyr580=) rs139188627 0.00008
NM_002834.5(PTPN11):c.1678C>T (p.Leu560Phe) rs397516797 0.00007
NM_002834.5(PTPN11):c.132C>T (p.Ser44=) rs397507502 0.00006
NM_002834.5(PTPN11):c.1682C>T (p.Pro561Leu) rs141140214 0.00006
NM_002834.5(PTPN11):c.392A>G (p.Lys131Arg) rs397516805 0.00006
NM_002834.5(PTPN11):c.426C>T (p.Ser142=) rs199498784 0.00006
NM_002834.5(PTPN11):c.616T>C (p.Leu206=) rs78376169 0.00006
NM_002834.5(PTPN11):c.990A>C (p.Thr330=) rs369739920 0.00005
NM_002834.5(PTPN11):c.1143C>T (p.Gly381=) rs781677115 0.00004
NM_002834.5(PTPN11):c.1278C>T (p.His426=) rs886038519 0.00004
NM_002834.5(PTPN11):c.893A>G (p.Asn298Ser) rs572274623 0.00004
NM_002834.5(PTPN11):c.1404G>C (p.Thr468=) rs587781130 0.00003
NM_002834.5(PTPN11):c.540C>T (p.Asp180=) rs753269427 0.00003
NM_002834.5(PTPN11):c.556C>T (p.Arg186Trp) rs143433437 0.00003
NM_002834.5(PTPN11):c.1551G>A (p.Ala517=) rs727504377 0.00002
NM_002834.5(PTPN11):c.327T>G (p.Ser109=) rs1039250039 0.00002
NM_002834.5(PTPN11):c.1011G>A (p.Thr337=) rs371951288 0.00001
NM_002834.5(PTPN11):c.1023T>C (p.Phe341=) rs762516252 0.00001
NM_002834.5(PTPN11):c.1047C>T (p.Asn349=) rs1222504763 0.00001
NM_002834.5(PTPN11):c.1131A>C (p.Leu377=) rs370059077 0.00001
NM_002834.5(PTPN11):c.1173C>T (p.Ser391=) rs770730416 0.00001
NM_002834.5(PTPN11):c.1176C>T (p.Ala392=) rs759533871 0.00001
NM_002834.5(PTPN11):c.1218T>C (p.Val406=) rs1402095646 0.00001
NM_002834.5(PTPN11):c.1404G>A (p.Thr468=) rs587781130 0.00001
NM_002834.5(PTPN11):c.1467C>T (p.Asp489=) rs539373294 0.00001
NM_002834.5(PTPN11):c.162C>T (p.Ile54=) rs1207829516 0.00001
NM_002834.5(PTPN11):c.1650G>A (p.Ala550=) rs374896287 0.00001
NM_002834.5(PTPN11):c.1659G>A (p.Thr553=) rs1381707337 0.00001
NM_002834.5(PTPN11):c.537C>T (p.Tyr179=) rs141015445 0.00001
NM_002834.5(PTPN11):c.874C>T (p.Leu292=) rs930267460 0.00001
NM_002834.5(PTPN11):c.951G>A (p.Lys317=) rs576405446 0.00001
NM_002834.5(PTPN11):c.957C>T (p.Asn319=) rs771407775 0.00001
NM_002834.5(PTPN11):c.996C>T (p.Gly332=) rs397507533 0.00001
NM_002834.5(PTPN11):c.108T>C (p.Ser36=)
NM_002834.5(PTPN11):c.1129C>T (p.Leu377=)
NM_002834.5(PTPN11):c.1242G>T (p.Thr414=) rs552394167
NM_002834.5(PTPN11):c.1266C>G (p.Thr422=) rs759848374
NM_002834.5(PTPN11):c.1281C>T (p.Gly427=) rs753173299
NM_002834.5(PTPN11):c.1365C>T (p.Val455=) rs1379099808
NM_002834.5(PTPN11):c.1530G>A (p.Gln510=)
NM_002834.5(PTPN11):c.156C>T (p.Thr52=)
NM_002834.5(PTPN11):c.1635T>C (p.Ile545=) rs1166186438
NM_002834.5(PTPN11):c.1692T>G (p.Thr564=)
NM_002834.5(PTPN11):c.1704C>T (p.Pro568=)
NM_002834.5(PTPN11):c.285C>A (p.Val95=)
NM_002834.5(PTPN11):c.438T>C (p.Asp146=) rs1566168661
NM_002834.5(PTPN11):c.456C>T (p.Arg152=)
NM_002834.5(PTPN11):c.528A>G (p.Glu176=)
NM_002834.5(PTPN11):c.555A>G (p.Glu185=)
NM_002834.5(PTPN11):c.615A>G (p.Thr205=) rs1592830197
NM_002834.5(PTPN11):c.6A>G (p.Thr2=) rs768238710
NM_002834.5(PTPN11):c.762A>G (p.Leu254=)
NM_002834.5(PTPN11):c.813A>G (p.Gln271=)
NM_002834.5(PTPN11):c.843C>T (p.Asn281=)
NM_002834.5(PTPN11):c.864C>G (p.Thr288=)
NM_002834.5(PTPN11):c.984T>C (p.Ile328=)

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