Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112477533_112477627delCA2621024323PTPN11c.854-118_854-24del (n.854-118_854-24del)
c.740-118_740-24del (n.740-118_740-24del)
c.851-118_851-24del (n.851-118_851-24del)
 gnomAD v4
12g.112477583A>GCA2575298902PTPN11c.854-68A>G (n.854-68A>G)
c.740-68A>G (n.740-68A>G)
c.851-68A>G (n.851-68A>G)
 gnomAD v4
12g.112477583A>TCA2727222002PTPN11c.854-68A>T (n.854-68A>T)
c.740-68A>T (n.740-68A>T)
c.851-68A>T (n.851-68A>T)
 dbSNP
12g.112477584C>ACA2621024423PTPN11c.854-67C>A (n.854-67C>A)
c.740-67C>A (n.740-67C>A)
c.851-67C>A (n.851-67C>A)
 gnomAD v4
12g.112477584C>GCA2575298903PTPN11c.854-67C>G (n.854-67C>G)
c.740-67C>G (n.740-67C>G)
c.851-67C>G (n.851-67C>G)
 dbSNP gnomAD v4
12g.112477585T>ACA2621024425PTPN11c.854-66T>A (n.854-66T>A)
c.740-66T>A (n.740-66T>A)
c.851-66T>A (n.851-66T>A)
 gnomAD v4
12g.112477586G>CCA2063775552PTPN11c.854-65G>C (n.854-65G>C)
c.740-65G>C (n.740-65G>C)
c.851-65G>C (n.851-65G>C)
 dbSNP
12g.112477586G=CA2063775553PTPN11c.854-65G= (n.854-65G=)
c.740-65G= (n.740-65G=)
c.851-65G= (n.851-65G=)
12g.112477586G>TCA243711872PTPN11c.854-65G>T (n.854-65G>T)
c.740-65G>T (n.740-65G>T)
c.851-65G>T (n.851-65G>T)
 dbSNP gnomAD v4
12g.112477587A>CCA2621024426PTPN11c.854-64A>C (n.854-64A>C)
c.740-64A>C (n.740-64A>C)
c.851-64A>C (n.851-64A>C)
 gnomAD v4
12g.112477588T>ACA683695372PTPN11c.854-63T>A (n.854-63T>A)
c.740-63T>A (n.740-63T>A)
c.851-63T>A (n.851-63T>A)
 dbSNP
12g.112477588T>CCA2621024428PTPN11c.854-63T>C (n.854-63T>C)
c.740-63T>C (n.740-63T>C)
c.851-63T>C (n.851-63T>C)
 gnomAD v4
12g.112477588T>GCA2621024430PTPN11c.854-63T>G (n.854-63T>G)
c.740-63T>G (n.740-63T>G)
c.851-63T>G (n.851-63T>G)
 gnomAD v4
12g.112477588T=CA2063775555PTPN11c.854-63T= (n.854-63T=)
c.740-63T= (n.740-63T=)
c.851-63T= (n.851-63T=)
12g.112477589T>ACA2063775558PTPN11c.854-62T>A (n.854-62T>A)
c.740-62T>A (n.740-62T>A)
c.851-62T>A (n.851-62T>A)
 dbSNP gnomAD v4
12g.112477589T>CCA2621024432PTPN11c.854-62T>C (n.854-62T>C)
c.740-62T>C (n.740-62T>C)
c.851-62T>C (n.851-62T>C)
 gnomAD v4
12g.112477589T=CA2063775557PTPN11c.854-62T= (n.854-62T=)
c.740-62T= (n.740-62T=)
c.851-62T= (n.851-62T=)
12g.112477590T>CCA2621024435PTPN11c.854-61T>C (n.854-61T>C)
c.740-61T>C (n.740-61T>C)
c.851-61T>C (n.851-61T>C)
 gnomAD v4
12g.112477590T>GCA2621024437PTPN11c.854-61T>G (n.854-61T>G)
c.740-61T>G (n.740-61T>G)
c.851-61T>G (n.851-61T>G)
 gnomAD v4
12g.112477591G>ACA2727222056PTPN11c.854-60G>A (n.854-60G>A)
c.740-60G>A (n.740-60G>A)
c.851-60G>A (n.851-60G>A)
 dbSNP
12g.112477591G>CCA2727222057PTPN11c.854-60G>C (n.854-60G>C)
c.740-60G>C (n.740-60G>C)
c.851-60G>C (n.851-60G>C)
 dbSNP
12g.112477591G>TCA2621024439PTPN11c.854-60G>T (n.854-60G>T)
c.740-60G>T (n.740-60G>T)
c.851-60G>T (n.851-60G>T)
 dbSNP gnomAD v4
12g.112477592A>CCA2727222084PTPN11c.854-59A>C (n.854-59A>C)
c.740-59A>C (n.740-59A>C)
c.851-59A>C (n.851-59A>C)
 dbSNP
12g.112477592A>TCA2727222133PTPN11c.854-59A>T (n.854-59A>T)
c.740-59A>T (n.740-59A>T)
c.851-59A>T (n.851-59A>T)
 dbSNP
12g.112477593A=CA2063775561PTPN11c.854-58A= (n.854-58A=)
c.740-58A= (n.740-58A=)
c.851-58A= (n.851-58A=)
12g.112477593A>CCA2621024441PTPN11c.854-58A>C (n.854-58A>C)
c.740-58A>C (n.740-58A>C)
c.851-58A>C (n.851-58A>C)
 gnomAD v4
12g.112477593A>GCA951950932PTPN11c.854-58A>G (n.854-58A>G)
c.740-58A>G (n.740-58A>G)
c.851-58A>G (n.851-58A>G)
 dbSNP gnomAD v3 gnomAD v4
12g.112477593A>TCA2727174327PTPN11c.854-58A>T (n.854-58A>T)
c.740-58A>T (n.740-58A>T)
c.851-58A>T (n.851-58A>T)
 dbSNP
12g.112477594C>ACA2621024443PTPN11c.854-57C>A (n.854-57C>A)
c.740-57C>A (n.740-57C>A)
c.851-57C>A (n.851-57C>A)
 dbSNP gnomAD v4
12g.112477594C>GCA2727222138PTPN11c.854-57C>G (n.854-57C>G)
c.740-57C>G (n.740-57C>G)
c.851-57C>G (n.851-57C>G)
 dbSNP
12g.112477594C>TCA2727222135PTPN11c.854-57C>T (n.854-57C>T)
c.740-57C>T (n.740-57C>T)
c.851-57C>T (n.851-57C>T)
 dbSNP
12g.112477595T>CCA2727222143PTPN11c.854-56T>C (n.854-56T>C)
c.740-56T>C (n.740-56T>C)
c.851-56T>C (n.851-56T>C)
 dbSNP
12g.112477596G>CCA243711875PTPN11c.854-55G>C (n.854-55G>C)
c.740-55G>C (n.740-55G>C)
c.851-55G>C (n.851-55G>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.112477596G=CA2063775564PTPN11c.854-55G= (n.854-55G=)
c.740-55G= (n.740-55G=)
c.851-55G= (n.851-55G=)
12g.112477596_112477597delinsGTCA2063775565PTPN11c.854-55_854-54delinsGT (n.854-55_854-54delinsGT)
c.740-55_740-54delinsGT (n.740-55_740-54delinsGT)
c.851-55_851-54delinsGT (n.851-55_851-54delinsGT)
12g.112477597T>ACA2063775568PTPN11c.854-54T>A (n.854-54T>A)
c.740-54T>A (n.740-54T>A)
c.851-54T>A (n.851-54T>A)
 dbSNP
12g.112477597T>CCA2621024453PTPN11c.854-54T>C (n.854-54T>C)
c.740-54T>C (n.740-54T>C)
c.851-54T>C (n.851-54T>C)
 gnomAD v4
12g.112477597T>GCA2727174328PTPN11c.854-54T>G (n.854-54T>G)
c.740-54T>G (n.740-54T>G)
c.851-54T>G (n.851-54T>G)
 dbSNP
12g.112477597T=CA2063775569PTPN11c.854-54T= (n.854-54T=)
c.740-54T= (n.740-54T=)
c.851-54T= (n.851-54T=)
12g.112477602dupCA2550309175PTPN11c.854-49dup (n.854-49dup)
c.740-49dup (n.740-49dup)
c.851-49dup (n.851-49dup)
 gnomAD v3 gnomAD v4
12g.112477602delCA683695381PTPN11c.854-49del (n.854-49del)
c.740-49del (n.740-49del)
c.851-49del (n.851-49del)
 dbSNP gnomAD v3 gnomAD v4
12g.112477598T>GCA243711877PTPN11c.854-53T>G (n.854-53T>G)
c.740-53T>G (n.740-53T>G)
c.851-53T>G (n.851-53T>G)
 dbSNP gnomAD v3 gnomAD v4
12g.112477598T=CA2063775571PTPN11c.854-53T= (n.854-53T=)
c.740-53T= (n.740-53T=)
c.851-53T= (n.851-53T=)
12g.112477599T>GCA2063775574PTPN11c.854-52T>G (n.854-52T>G)
c.740-52T>G (n.740-52T>G)
c.851-52T>G (n.851-52T>G)
 dbSNP gnomAD v4
12g.112477599T=CA2063775573PTPN11c.854-52T= (n.854-52T=)
c.740-52T= (n.740-52T=)
c.851-52T= (n.851-52T=)
12g.112477601T>CCA2621024460PTPN11c.854-50T>C (n.854-50T>C)
c.740-50T>C (n.740-50T>C)
c.851-50T>C (n.851-50T>C)
 gnomAD v4
12g.112477603C>ACA2621024461PTPN11c.854-48C>A (n.854-48C>A)
c.740-48C>A (n.740-48C>A)
c.851-48C>A (n.851-48C>A)
 gnomAD v4
12g.112477603C=CA2063775575PTPN11c.854-48C= (n.854-48C=)
c.740-48C= (n.740-48C=)
c.851-48C= (n.851-48C=)
12g.112477603C>TCA2063775576PTPN11c.854-48C>T (n.854-48C>T)
c.740-48C>T (n.740-48C>T)
c.851-48C>T (n.851-48C>T)
 dbSNP gnomAD v4
12g.112477603_112477612delCA2797498055PTPN11c.854-48_854-39del (n.854-48_854-39del)
c.740-48_740-39del (n.740-48_740-39del)
c.851-48_851-39del (n.851-48_851-39del)
12g.112477604C>ACA2621024462PTPN11c.854-47C>A (n.854-47C>A)
c.740-47C>A (n.740-47C>A)
c.851-47C>A (n.851-47C>A)
 gnomAD v4
12g.112477604C=CA2063775578PTPN11c.854-47C= (n.854-47C=)
c.740-47C= (n.740-47C=)
c.851-47C= (n.851-47C=)
12g.112477604C>GCA2063775580PTPN11c.854-47C>G (n.854-47C>G)
c.740-47C>G (n.740-47C>G)
c.851-47C>G (n.851-47C>G)
 dbSNP gnomAD v4
12g.112477604C>TCA2727174329PTPN11c.854-47C>T (n.854-47C>T)
c.740-47C>T (n.740-47C>T)
c.851-47C>T (n.851-47C>T)
 dbSNP
12g.112477605T>CCA2621024465PTPN11c.854-46T>C (n.854-46T>C)
c.740-46T>C (n.740-46T>C)
c.851-46T>C (n.851-46T>C)
 dbSNP gnomAD v4
12g.112477605T>GCA2621024464PTPN11c.854-46T>G (n.854-46T>G)
c.740-46T>G (n.740-46T>G)
c.851-46T>G (n.851-46T>G)
 gnomAD v4
12g.112477606G>ACA2727222364PTPN11c.854-45G>A (n.854-45G>A)
c.740-45G>A (n.740-45G>A)
c.851-45G>A (n.851-45G>A)
 dbSNP
12g.112477606G>CCA2727222369PTPN11c.854-45G>C (n.854-45G>C)
c.740-45G>C (n.740-45G>C)
c.851-45G>C (n.851-45G>C)
 dbSNP
12g.112477606G>TCA2727222409PTPN11c.854-45G>T (n.854-45G>T)
c.740-45G>T (n.740-45G>T)
c.851-45G>T (n.851-45G>T)
 dbSNP
12g.112477607A>GCA2575298908PTPN11c.854-44A>G (n.854-44A>G)
c.740-44A>G (n.740-44A>G)
c.851-44A>G (n.851-44A>G)
12g.112477607A>TCA2727222424PTPN11c.854-44A>T (n.854-44A>T)
c.740-44A>T (n.740-44A>T)
c.851-44A>T (n.851-44A>T)
 dbSNP
12g.112477608A=CA2063775582PTPN11c.854-43A= (n.854-43A=)
c.740-43A= (n.740-43A=)
c.851-43A= (n.851-43A=)
12g.112477608A>GCA6798663PTPN11c.854-43A>G (n.854-43A>G)
c.740-43A>G (n.740-43A>G)
c.851-43A>G (n.851-43A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477608A>TCA2727053170PTPN11c.854-43A>T (n.854-43A>T)
c.740-43A>T (n.740-43A>T)
c.851-43A>T (n.851-43A>T)
 dbSNP
12g.112477609G>ACA2727222443PTPN11c.854-42G>A (n.854-42G>A)
c.740-42G>A (n.740-42G>A)
c.851-42G>A (n.851-42G>A)
 dbSNP
12g.112477609G>CCA2727222485PTPN11c.854-42G>C (n.854-42G>C)
c.740-42G>C (n.740-42G>C)
c.851-42G>C (n.851-42G>C)
 dbSNP
12g.112477610C>ACA2575298909PTPN11c.854-41C>A (n.854-41C>A)
c.740-41C>A (n.740-41C>A)
c.851-41C>A (n.851-41C>A)
 gnomAD v4
12g.112477610C>GCA2621024471PTPN11c.854-41C>G (n.854-41C>G)
c.740-41C>G (n.740-41C>G)
c.851-41C>G (n.851-41C>G)
 dbSNP gnomAD v4
12g.112477610C>TCA2727222556PTPN11c.854-41C>T (n.854-41C>T)
c.740-41C>T (n.740-41C>T)
c.851-41C>T (n.851-41C>T)
 dbSNP
12g.112477611A=CA2063775586PTPN11c.854-40A= (n.854-40A=)
c.740-40A= (n.740-40A=)
c.851-40A= (n.851-40A=)
12g.112477611A>GCA6798664PTPN11c.854-40A>G (n.854-40A>G)
c.740-40A>G (n.740-40A>G)
c.851-40A>G (n.851-40A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.112477612G>CCA2727222612PTPN11c.854-39G>C (n.854-39G>C)
c.740-39G>C (n.740-39G>C)
c.851-39G>C (n.851-39G>C)
 dbSNP
12g.112477612G>TCA2621024477PTPN11c.854-39G>T (n.854-39G>T)
c.740-39G>T (n.740-39G>T)
c.851-39G>T (n.851-39G>T)
 gnomAD v4
12g.112477613T>ACA2727174330PTPN11c.854-38T>A (n.854-38T>A)
c.740-38T>A (n.740-38T>A)
c.851-38T>A (n.851-38T>A)
 dbSNP
12g.112477613T>CCA2063775592PTPN11c.854-38T>C (n.854-38T>C)
c.740-38T>C (n.740-38T>C)
c.851-38T>C (n.851-38T>C)
 dbSNP gnomAD v4
12g.112477613T>GCA2575298911PTPN11c.854-38T>G (n.854-38T>G)
c.740-38T>G (n.740-38T>G)
c.851-38T>G (n.851-38T>G)
 dbSNP
12g.112477613T=CA2063775590PTPN11c.854-38T= (n.854-38T=)
c.740-38T= (n.740-38T=)
c.851-38T= (n.851-38T=)
12g.112477614C>ACA2621024488PTPN11c.854-37C>A (n.854-37C>A)
c.740-37C>A (n.740-37C>A)
c.851-37C>A (n.851-37C>A)
 gnomAD v4
12g.112477614C=CA2063775594PTPN11c.854-37C= (n.854-37C=)
c.740-37C= (n.740-37C=)
c.851-37C= (n.851-37C=)
12g.112477614C>GCA2727061519PTPN11c.854-37C>G (n.854-37C>G)
c.740-37C>G (n.740-37C>G)
c.851-37C>G (n.851-37C>G)
 dbSNP
12g.112477614C>TCA243711878PTPN11c.854-37C>T (n.854-37C>T)
c.740-37C>T (n.740-37C>T)
c.851-37C>T (n.851-37C>T)
 dbSNP gnomAD v4
12g.112477615C>ACA2621024490PTPN11c.854-36C>A (n.854-36C>A)
c.740-36C>A (n.740-36C>A)
c.851-36C>A (n.851-36C>A)
 dbSNP gnomAD v4
12g.112477615C=CA2063775595PTPN11c.854-36C= (n.854-36C=)
c.740-36C= (n.740-36C=)
c.851-36C= (n.851-36C=)
12g.112477615C>GCA2621024491PTPN11c.854-36C>G (n.854-36C>G)
c.740-36C>G (n.740-36C>G)
c.851-36C>G (n.851-36C>G)
 gnomAD v4
12g.112477615C>TCA2063775596PTPN11c.854-36C>T (n.854-36C>T)
c.740-36C>T (n.740-36C>T)
c.851-36C>T (n.851-36C>T)
 dbSNP gnomAD v4
12g.112477616A=CA2063775598PTPN11c.854-35A= (n.854-35A=)
c.740-35A= (n.740-35A=)
c.851-35A= (n.851-35A=)
12g.112477616A>CCA6798665PTPN11c.854-35A>C (n.854-35A>C)
c.740-35A>C (n.740-35A>C)
c.851-35A>C (n.851-35A>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477616A>TCA2727058027PTPN11c.854-35A>T (n.854-35A>T)
c.740-35A>T (n.740-35A>T)
c.851-35A>T (n.851-35A>T)
 dbSNP
12g.112477617G>ACA2727222613PTPN11c.854-34G>A (n.854-34G>A)
c.740-34G>A (n.740-34G>A)
c.851-34G>A (n.851-34G>A)
 dbSNP
12g.112477617G>CCA2727222614PTPN11c.854-34G>C (n.854-34G>C)
c.740-34G>C (n.740-34G>C)
c.851-34G>C (n.851-34G>C)
 dbSNP
12g.112477617G>TCA2727222656PTPN11c.854-34G>T (n.854-34G>T)
c.740-34G>T (n.740-34G>T)
c.851-34G>T (n.851-34G>T)
 dbSNP
12g.112477618G>ACA2621024496PTPN11c.854-33G>A (n.854-33G>A)
c.740-33G>A (n.740-33G>A)
c.851-33G>A (n.851-33G>A)
 dbSNP gnomAD v4
12g.112477618G>CCA2727222697PTPN11c.854-33G>C (n.854-33G>C)
c.740-33G>C (n.740-33G>C)
c.851-33G>C (n.851-33G>C)
 dbSNP
12g.112477619A=CA2063775601PTPN11c.854-32A= (n.854-32A=)
c.740-32A= (n.740-32A=)
c.851-32A= (n.851-32A=)
12g.112477619A>CCA215447PTPN11c.854-32A>C (n.854-32A>C)
c.740-32A>C (n.740-32A>C)
c.851-32A>C (n.851-32A>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477619A>TCA2727051824PTPN11c.854-32A>T (n.854-32A>T)
c.740-32A>T (n.740-32A>T)
c.851-32A>T (n.851-32A>T)
 dbSNP
12g.112477620C>ACA2621024499PTPN11c.854-31C>A (n.854-31C>A)
c.740-31C>A (n.740-31C>A)
c.851-31C>A (n.851-31C>A)
 dbSNP gnomAD v4
12g.112477620C=CA2063775603PTPN11c.854-31C= (n.854-31C=)
c.740-31C= (n.740-31C=)
c.851-31C= (n.851-31C=)
12g.112477620C>GCA2727092207PTPN11c.854-31C>G (n.854-31C>G)
c.740-31C>G (n.740-31C>G)
c.851-31C>G (n.851-31C>G)
 dbSNP
12g.112477620C>TCA607604962PTPN11c.854-31C>T (n.854-31C>T)
c.740-31C>T (n.740-31C>T)
c.851-31C>T (n.851-31C>T)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
12g.112477621T>CCA130822PTPN11c.854-30T>C (n.854-30T>C)
c.740-30T>C (n.740-30T>C)
c.851-30T>C (n.851-30T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477621T=CA2063775605PTPN11c.854-30T= (n.854-30T=)
c.740-30T= (n.740-30T=)
c.851-30T= (n.851-30T=)
12g.112477622T>CCA2727222760PTPN11c.854-29T>C (n.854-29T>C)
c.740-29T>C (n.740-29T>C)
c.851-29T>C (n.851-29T>C)
 dbSNP
12g.112477623A>GCA2727222780PTPN11c.854-28A>G (n.854-28A>G)
c.740-28A>G (n.740-28A>G)
c.851-28A>G (n.851-28A>G)
 dbSNP
12g.112477623A>TCA2727222781PTPN11c.854-28A>T (n.854-28A>T)
c.740-28A>T (n.740-28A>T)
c.851-28A>T (n.851-28A>T)
 dbSNP
12g.112477623dupCA2621024501PTPN11c.854-28dup (n.854-28dup)
c.740-28dup (n.740-28dup)
c.851-28dup (n.851-28dup)
 gnomAD v4
12g.112477624T>ACA607604964PTPN11c.854-27T>A (n.854-27T>A)
c.740-27T>A (n.740-27T>A)
c.851-27T>A (n.851-27T>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.112477624T>CCA607604966PTPN11c.854-27T>C (n.854-27T>C)
c.740-27T>C (n.740-27T>C)
c.851-27T>C (n.851-27T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.112477624T=CA2063775607PTPN11c.854-27T= (n.854-27T=)
c.740-27T= (n.740-27T=)
c.851-27T= (n.851-27T=)
12g.112477625G>ACA607604967PTPN11c.854-26G>A (n.854-26G>A)
c.740-26G>A (n.740-26G>A)
c.851-26G>A (n.851-26G>A)
 dbSNP gnomAD v2 gnomAD v4
12g.112477625G>CCA2727094909PTPN11c.854-26G>C (n.854-26G>C)
c.740-26G>C (n.740-26G>C)
c.851-26G>C (n.851-26G>C)
 dbSNP
12g.112477625G=CA2063775609PTPN11c.854-26G= (n.854-26G=)
c.740-26G= (n.740-26G=)
c.851-26G= (n.851-26G=)
12g.112477626T>ACA2727222798PTPN11c.854-25T>A (n.854-25T>A)
c.740-25T>A (n.740-25T>A)
c.851-25T>A (n.851-25T>A)
 dbSNP
12g.112477627G>ACA2621024508PTPN11c.854-24G>A (n.854-24G>A)
c.740-24G>A (n.740-24G>A)
c.851-24G>A (n.851-24G>A)
 gnomAD v4
12g.112477627G>CCA2727222865PTPN11c.854-24G>C (n.854-24G>C)
c.740-24G>C (n.740-24G>C)
c.851-24G>C (n.851-24G>C)
 dbSNP
12g.112477627G>TCA2621024509PTPN11c.854-24G>T (n.854-24G>T)
c.740-24G>T (n.740-24G>T)
c.851-24G>T (n.851-24G>T)
 gnomAD v4
12g.112477628A>GCA2575298931PTPN11c.854-23A>G (n.854-23A>G)
c.740-23A>G (n.740-23A>G)
c.851-23A>G (n.851-23A>G)
 gnomAD v4
12g.112477628A>TCA2727222879PTPN11c.854-23A>T (n.854-23A>T)
c.740-23A>T (n.740-23A>T)
c.851-23A>T (n.851-23A>T)
 dbSNP
12g.112477629C>ACA2621024512PTPN11c.854-22C>A (n.854-22C>A)
c.740-22C>A (n.740-22C>A)
c.851-22C>A (n.851-22C>A)
 dbSNP gnomAD v4
12g.112477629C=CA2063775612PTPN11c.854-22C= (n.854-22C=)
c.740-22C= (n.740-22C=)
c.851-22C= (n.851-22C=)
12g.112477629C>GCA2727099586PTPN11c.854-22C>G (n.854-22C>G)
c.740-22C>G (n.740-22C>G)
c.851-22C>G (n.851-22C>G)
 dbSNP
12g.112477629C>TCA2063775611PTPN11c.854-22C>T (n.854-22C>T)
c.740-22C>T (n.740-22C>T)
c.851-22C>T (n.851-22C>T)
 dbSNP
12g.112477630C>ACA2063775617PTPN11c.854-21C>A (n.854-21C>A)
c.740-21C>A (n.740-21C>A)
c.851-21C>A (n.851-21C>A)
 dbSNP gnomAD v4
12g.112477630C=CA2063775614PTPN11c.854-21C= (n.854-21C=)
c.740-21C= (n.740-21C=)
c.851-21C= (n.851-21C=)
12g.112477630C>GCA6798666PTPN11c.854-21C>G (n.854-21C>G)
c.740-21C>G (n.740-21C>G)
c.851-21C>G (n.851-21C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477630C>TCA130823PTPN11c.854-21C>T (n.854-21C>T)
c.740-21C>T (n.740-21C>T)
c.851-21C>T (n.851-21C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477631delCA2621024528PTPN11c.854-20del (n.854-20del)
c.740-20del (n.740-20del)
c.851-20del (n.851-20del)
 gnomAD v4
12g.112477631G>ACA6798667PTPN11c.854-20G>A (n.854-20G>A)
c.740-20G>A (n.740-20G>A)
c.851-20G>A (n.851-20G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477631G>CCA2727057125PTPN11c.854-20G>C (n.854-20G>C)
c.740-20G>C (n.740-20G>C)
c.851-20G>C (n.851-20G>C)
 dbSNP
12g.112477631G=CA2063775620PTPN11c.854-20G= (n.854-20G=)
c.740-20G= (n.740-20G=)
c.851-20G= (n.851-20G=)
12g.112477631G>TCA2621024526PTPN11c.854-20G>T (n.854-20G>T)
c.740-20G>T (n.740-20G>T)
c.851-20G>T (n.851-20G>T)
 dbSNP gnomAD v4
12g.112477632T>ACA2621024532PTPN11c.854-19T>A (n.854-19T>A)
c.740-19T>A (n.740-19T>A)
c.851-19T>A (n.851-19T>A)
 gnomAD v4
12g.112477632T>CCA2621024533PTPN11c.854-19T>C (n.854-19T>C)
c.740-19T>C (n.740-19T>C)
c.851-19T>C (n.851-19T>C)
 gnomAD v4
12g.112477632T>GCA6798668PTPN11c.854-19T>G (n.854-19T>G)
c.740-19T>G (n.740-19T>G)
c.851-19T>G (n.851-19T>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477632T=CA2063775622PTPN11c.854-19T= (n.854-19T=)
c.740-19T= (n.740-19T=)
c.851-19T= (n.851-19T=)
12g.112477633G>CCA6798669PTPN11c.854-18G>C (n.854-18G>C)
c.740-18G>C (n.740-18G>C)
c.851-18G>C (n.851-18G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477633G=CA2063775625PTPN11c.854-18G= (n.854-18G=)
c.740-18G= (n.740-18G=)
c.851-18G= (n.851-18G=)
12g.112477634delCA2621024536PTPN11c.854-17del (n.854-17del)
c.740-17del (n.740-17del)
c.851-17del (n.851-17del)
 gnomAD v4
12g.112477634G>ACA2575298954PTPN11c.854-17G>A (n.854-17G>A)
c.740-17G>A (n.740-17G>A)
c.851-17G>A (n.851-17G>A)
 ClinVar dbSNP gnomAD v4
12g.112477634G>CCA2727052761PTPN11c.854-17G>C (n.854-17G>C)
c.740-17G>C (n.740-17G>C)
c.851-17G>C (n.851-17G>C)
 dbSNP
12g.112477634G=CA2063775627PTPN11c.854-17G= (n.854-17G=)
c.740-17G= (n.740-17G=)
c.851-17G= (n.851-17G=)
12g.112477634G>TCA6798670PTPN11c.854-17G>T (n.854-17G>T)
c.740-17G>T (n.740-17G>T)
c.851-17G>T (n.851-17G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477635T>ACA951951009PTPN11c.854-16T>A (n.854-16T>A)
c.740-16T>A (n.740-16T>A)
c.851-16T>A (n.851-16T>A)
 dbSNP gnomAD v3 gnomAD v4
12g.112477635T=CA2063775629PTPN11c.854-16T= (n.854-16T=)
c.740-16T= (n.740-16T=)
c.851-16T= (n.851-16T=)
12g.112477638_112477639delCA2621024546PTPN11c.854-13_854-12del (n.854-13_854-12del)
c.740-13_740-12del (n.740-13_740-12del)
c.851-13_851-12del (n.851-13_851-12del)
 ClinVar gnomAD v4
12g.112477636C=CA2063775631PTPN11c.854-15C= (n.854-15C=)
c.740-15C= (n.740-15C=)
c.851-15C= (n.851-15C=)
12g.112477636C>GCA2727058939PTPN11c.854-15C>G (n.854-15C>G)
c.740-15C>G (n.740-15C>G)
c.851-15C>G (n.851-15C>G)
 dbSNP
12g.112477636C>TCA6798671PTPN11c.854-15C>T (n.854-15C>T)
c.740-15C>T (n.740-15C>T)
c.851-15C>T (n.851-15C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477637T>ACA1139662891PTPN11c.854-14T>A (n.854-14T>A)
c.740-14T>A (n.740-14T>A)
c.851-14T>A (n.851-14T>A)
 ClinVar dbSNP gnomAD v4
12g.112477637T=CA2063775636PTPN11c.854-14T= (n.854-14T=)
c.740-14T= (n.740-14T=)
c.851-14T= (n.851-14T=)
12g.112477638C>ACA2727222881PTPN11c.854-13C>A (n.854-13C>A)
c.740-13C>A (n.740-13C>A)
c.851-13C>A (n.851-13C>A)
 dbSNP
12g.112477639T>ACA2727222963PTPN11c.854-12T>A (n.854-12T>A)
c.740-12T>A (n.740-12T>A)
c.851-12T>A (n.851-12T>A)
 dbSNP
12g.112477639T>CCA2727223071PTPN11c.854-12T>C (n.854-12T>C)
c.740-12T>C (n.740-12T>C)
c.851-12T>C (n.851-12T>C)
 dbSNP
12g.112477639T>GCA2727223072PTPN11c.854-12T>G (n.854-12T>G)
c.740-12T>G (n.740-12T>G)
c.851-12T>G (n.851-12T>G)
 dbSNP
12g.112477643delCA2575298955PTPN11c.854-8del (n.854-8del)
c.740-8del (n.740-8del)
c.851-8del (n.851-8del)
 gnomAD v4
12g.112477641T>CCA683695435PTPN11c.854-10T>C (n.854-10T>C)
c.740-10T>C (n.740-10T>C)
c.851-10T>C (n.851-10T>C)
 dbSNP gnomAD v3 gnomAD v4
12g.112477641T=CA2063775639PTPN11c.854-10T= (n.854-10T=)
c.740-10T= (n.740-10T=)
c.851-10T= (n.851-10T=)
12g.112477642T>CCA2063775642PTPN11c.854-9T>C (n.854-9T>C)
c.740-9T>C (n.740-9T>C)
c.851-9T>C (n.851-9T>C)
 dbSNP gnomAD v4
12g.112477642T=CA2063775641PTPN11c.854-9T= (n.854-9T=)
c.740-9T= (n.740-9T=)
c.851-9T= (n.851-9T=)
12g.112477643T>CCA6798672PTPN11c.854-8T>C (n.854-8T>C)
c.740-8T>C (n.740-8T>C)
c.851-8T>C (n.851-8T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477643T=CA2063775644PTPN11c.854-8T= (n.854-8T=)
c.740-8T= (n.740-8T=)
c.851-8T= (n.851-8T=)
12g.112477644C>GCA2727223073PTPN11c.854-7C>G (n.854-7C>G)
c.740-7C>G (n.740-7C>G)
c.851-7C>G (n.851-7C>G)
 dbSNP
12g.112477644C>TCA2621024553PTPN11c.854-7C>T (n.854-7C>T)
c.740-7C>T (n.740-7C>T)
c.851-7C>T (n.851-7C>T)
 dbSNP gnomAD v4
12g.112477645T>ACA2621024554PTPN11c.854-6T>A (n.854-6T>A)
c.740-6T>A (n.740-6T>A)
c.851-6T>A (n.851-6T>A)
 gnomAD v4
12g.112477645T>CCA2063775647PTPN11c.854-6T>C (n.854-6T>C)
c.740-6T>C (n.740-6T>C)
c.851-6T>C (n.851-6T>C)
 dbSNP
12g.112477645T=CA2063775646PTPN11c.854-6T= (n.854-6T=)
c.740-6T= (n.740-6T=)
c.851-6T= (n.851-6T=)
12g.112477647C>ACA2727223075PTPN11c.854-4C>A (n.854-4C>A)
c.740-4C>A (n.740-4C>A)
c.851-4C>A (n.851-4C>A)
 dbSNP
12g.112477647C>GCA2727223112PTPN11c.854-4C>G (n.854-4C>G)
c.740-4C>G (n.740-4C>G)
c.851-4C>G (n.851-4C>G)
 dbSNP
12g.112477647C>TCA2621024555PTPN11c.854-4C>T (n.854-4C>T)
c.740-4C>T (n.740-4C>T)
c.851-4C>T (n.851-4C>T)
 dbSNP gnomAD v4
12g.112477649A>CCA386790389PTPN11c.854-2A>C (n.854-2A>C)
c.740-2A>C (n.740-2A>C)
c.851-2A>C (n.851-2A>C)
12g.112477649A>GCA386790391PTPN11c.854-2A>G (n.854-2A>G)
c.740-2A>G (n.740-2A>G)
c.851-2A>G (n.851-2A>G)
12g.112477649A>TCA386790392PTPN11c.854-2A>T (n.854-2A>T)
c.740-2A>T (n.740-2A>T)
c.851-2A>T (n.851-2A>T)
 dbSNP gnomAD v4
12g.112477650G>ACA386790401PTPN11c.854-1G>A (n.854-1G>A)
c.740-1G>A (n.740-1G>A)
c.851-1G>A (n.851-1G>A)
12g.112477650G>CCA386790396PTPN11c.854-1G>C (n.854-1G>C)
c.740-1G>C (n.740-1G>C)
c.851-1G>C (n.851-1G>C)
 ClinVar dbSNP
12g.112477650G=CA2063775650PTPN11c.854-1G= (n.854-1G=)
c.740-1G= (n.740-1G=)
c.851-1G= (n.851-1G=)
12g.112477650G>TCA386790398PTPN11c.854-1G>T (n.854-1G>T)
c.740-1G>T (n.740-1G>T)
c.851-1G>T (n.851-1G>T)
 gnomAD v4
12g.112477651T>ACA297085PTPN11c.854T>A (p.Phe285Tyr)
c.740T>A (p.Phe247Tyr)
c.851T>A (p.Phe284Tyr)
 ClinVar dbSNP
12g.112477651T>CCA204408PTPN11c.854T>C (p.Phe285Ser)
c.740T>C (p.Phe247Ser)
c.851T>C (p.Phe284Ser)
 ClinVar dbSNP COSMIC
12g.112477651T>GCA261603PTPN11c.854T>G (p.Phe285Cys)
c.740T>G (p.Phe247Cys)
c.851T>G (p.Phe284Cys)
 ClinVar dbSNP
12g.112477651T=CA2063775659PTPN11c.854T= (p.Phe285=)
c.740T= (p.Phe247=)
c.851T= (p.Phe284=)
12g.112477652T>ACA386790412PTPN11c.855T>A (p.Phe285Leu)
c.741T>A (p.Phe247Leu)
c.852T>A (p.Phe284Leu)
 ClinVar dbSNP gnomAD v4
12g.112477652T>CCA481887633PTPN11c.855T>C (p.Phe285=)
c.741T>C (p.Phe247=)
c.852T>C (p.Phe284=)
12g.112477652T>GCA261606PTPN11c.855T>G (p.Phe285Leu)
c.741T>G (p.Phe247Leu)
c.852T>G (p.Phe284Leu)
 ClinVar dbSNP
12g.112477652T=CA2063775668PTPN11c.855T= (p.Phe285=)
c.741T= (p.Phe247=)
c.852T= (p.Phe284=)
12g.112477653G>ACA386790419PTPN11c.856G>A (p.Asp286Asn)
c.742G>A (p.Asp248Asn)
c.853G>A (p.Asp285Asn)
12g.112477653G>CCA386790414PTPN11c.856G>C (p.Asp286His)
c.742G>C (p.Asp248His)
c.853G>C (p.Asp285His)
 dbSNP
12g.112477653G>TCA386790416PTPN11c.856G>T (p.Asp286Tyr)
c.742G>T (p.Asp248Tyr)
c.853G>T (p.Asp285Tyr)
 gnomAD v4
12g.112477654A>CCA386790422PTPN11c.857A>C (p.Asp286Ala)
c.743A>C (p.Asp248Ala)
c.854A>C (p.Asp285Ala)
12g.112477654A>GCA386790424PTPN11c.857A>G (p.Asp286Gly)
c.743A>G (p.Asp248Gly)
c.854A>G (p.Asp285Gly)
12g.112477654A>TCA386790429PTPN11c.857A>T (p.Asp286Val)
c.743A>T (p.Asp248Val)
c.854A>T (p.Asp285Val)
 dbSNP gnomAD v4 COSMIC
12g.112477655T>ACA134683PTPN11c.858T>A (p.Asp286Glu)
c.744T>A (p.Asp248Glu)
c.855T>A (p.Asp285Glu)
 ClinVar dbSNP
12g.112477655T>CCA481887634PTPN11c.858T>C (p.Asp286=)
c.744T>C (p.Asp248=)
c.855T>C (p.Asp285=)
12g.112477655T>GCA386790433PTPN11c.858T>G (p.Asp286Glu)
c.744T>G (p.Asp248Glu)
c.855T>G (p.Asp285Glu)
12g.112477655T=CA2063775675PTPN11c.858T= (p.Asp286=)
c.744T= (p.Asp248=)
c.855T= (p.Asp285=)
12g.112477656C>ACA386790436PTPN11c.859C>A (p.His287Asn)
c.745C>A (p.His249Asn)
c.856C>A (p.His286Asn)
 gnomAD v4
12g.112477656C>GCA386790438PTPN11c.859C>G (p.His287Asp)
c.745C>G (p.His249Asp)
c.856C>G (p.His286Asp)
 dbSNP
12g.112477656C>TCA386790440PTPN11c.859C>T (p.His287Tyr)
c.745C>T (p.His249Tyr)
c.856C>T (p.His286Tyr)
 dbSNP
12g.112477657A=CA2063775679PTPN11c.860A= (p.His287=)
c.746A= (p.His249=)
c.857A= (p.His286=)
12g.112477657A>CCA386790444PTPN11c.860A>C (p.His287Pro)
c.746A>C (p.His249Pro)
c.857A>C (p.His286Pro)
 ClinVar dbSNP gnomAD v3 gnomAD v4
12g.112477657A>GCA386790446PTPN11c.860A>G (p.His287Arg)
c.746A>G (p.His249Arg)
c.857A>G (p.His286Arg)
12g.112477657A>TCA386790449PTPN11c.860A>T (p.His287Leu)
c.746A>T (p.His249Leu)
c.857A>T (p.His286Leu)
 dbSNP
12g.112477658T>ACA386790453PTPN11c.861T>A (p.His287Gln)
c.747T>A (p.His249Gln)
c.858T>A (p.His286Gln)
12g.112477658T>CCA243711913PTPN11c.861T>C (p.His287=)
c.747T>C (p.His249=)
c.858T>C (p.His286=)
 ClinVar dbSNP
12g.112477658T>GCA386790455PTPN11c.861T>G (p.His287Gln)
c.747T>G (p.His249Gln)
c.858T>G (p.His286Gln)
12g.112477658T=CA2063775684PTPN11c.861T= (p.His287=)
c.747T= (p.His249=)
c.858T= (p.His286=)
12g.112477659A>CCA386790459PTPN11c.862A>C (p.Thr288Pro)
c.748A>C (p.Thr250Pro)
c.859A>C (p.Thr287Pro)
12g.112477659A>GCA386790465PTPN11c.862A>G (p.Thr288Ala)
c.748A>G (p.Thr250Ala)
c.859A>G (p.Thr287Ala)
 ClinVar dbSNP gnomAD v4
12g.112477659A>TCA386790462PTPN11c.862A>T (p.Thr288Ser)
c.748A>T (p.Thr250Ser)
c.859A>T (p.Thr287Ser)
 dbSNP
12g.112477660C>ACA386790467PTPN11c.863C>A (p.Thr288Asn)
c.749C>A (p.Thr250Asn)
c.860C>A (p.Thr287Asn)
 dbSNP
12g.112477660C>GCA386790470PTPN11c.863C>G (p.Thr288Ser)
c.749C>G (p.Thr250Ser)
c.860C>G (p.Thr287Ser)
 dbSNP
12g.112477660C>TCA386790473PTPN11c.863C>T (p.Thr288Ile)
c.749C>T (p.Thr250Ile)
c.860C>T (p.Thr287Ile)
 dbSNP COSMIC
12g.112477661C>ACA481887635PTPN11c.864C>A (p.Thr288=)
c.750C>A (p.Thr250=)
c.861C>A (p.Thr287=)
 dbSNP gnomAD v4
12g.112477661C>GCA481887636PTPN11c.864C>G (p.Thr288=)
c.750C>G (p.Thr250=)
c.861C>G (p.Thr287=)
 ClinVar dbSNP gnomAD v4
12g.112477661C>TCA481887637PTPN11c.864C>T (p.Thr288=)
c.750C>T (p.Thr250=)
c.861C>T (p.Thr287=)
 dbSNP
12g.112477662A>CCA481887638PTPN11c.865A>C (p.Arg289=)
c.751A>C (p.Arg251=)
c.862A>C (p.Arg288=)
12g.112477662A>GCA386790475PTPN11c.865A>G (p.Arg289Gly)
c.751A>G (p.Arg251Gly)
c.862A>G (p.Arg288Gly)
 ClinVar dbSNP
12g.112477662A>TCA386790477PTPN11c.865A>T (p.Arg289Trp)
c.751A>T (p.Arg251Trp)
c.862A>T (p.Arg288Trp)
12g.112477663G>ACA386790480PTPN11c.866G>A (p.Arg289Lys)
c.752G>A (p.Arg251Lys)
c.863G>A (p.Arg288Lys)
12g.112477663G>CCA386790481PTPN11c.866G>C (p.Arg289Thr)
c.752G>C (p.Arg251Thr)
c.863G>C (p.Arg288Thr)
12g.112477663G>TCA386790483PTPN11c.866G>T (p.Arg289Met)
c.752G>T (p.Arg251Met)
c.863G>T (p.Arg288Met)
12g.112477664G>ACA481887639PTPN11c.867G>A (p.Arg289=)
c.753G>A (p.Arg251=)
c.864G>A (p.Arg288=)
 dbSNP gnomAD v3 gnomAD v4
12g.112477664G>CCA386790485PTPN11c.867G>C (p.Arg289Ser)
c.753G>C (p.Arg251Ser)
c.864G>C (p.Arg288Ser)
 ClinVar dbSNP gnomAD v4
12g.112477664G=CA2063775689PTPN11c.867G= (p.Arg289=)
c.753G= (p.Arg251=)
c.864G= (p.Arg288=)
12g.112477664G>TCA386790488PTPN11c.867G>T (p.Arg289Ser)
c.753G>T (p.Arg251Ser)
c.864G>T (p.Arg288Ser)
 dbSNP gnomAD v4
12g.112477665G>ACA386790490PTPN11c.868G>A (p.Val290Ile)
c.754G>A (p.Val252Ile)
c.865G>A (p.Val289Ile)
 ClinVar dbSNP
12g.112477665G>CCA386790492PTPN11c.868G>C (p.Val290Leu)
c.754G>C (p.Val252Leu)
c.865G>C (p.Val289Leu)
 ClinVar dbSNP
12g.112477665G=CA2063775693PTPN11c.868G= (p.Val290=)
c.754G= (p.Val252=)
c.865G= (p.Val289=)
12g.112477665G>TCA386790495PTPN11c.868G>T (p.Val290Phe)
c.754G>T (p.Val252Phe)
c.865G>T (p.Val289Phe)
 dbSNP
12g.112477666T>ACA386790505PTPN11c.869T>A (p.Val290Asp)
c.755T>A (p.Val252Asp)
c.866T>A (p.Val289Asp)
 dbSNP
12g.112477666T>CCA386790498PTPN11c.869T>C (p.Val290Ala)
c.755T>C (p.Val252Ala)
c.866T>C (p.Val289Ala)
 dbSNP gnomAD v2 gnomAD v4
12g.112477666T>GCA386790502PTPN11c.869T>G (p.Val290Gly)
c.755T>G (p.Val252Gly)
c.866T>G (p.Val289Gly)
12g.112477666T=CA2063775697PTPN11c.869T= (p.Val290=)
c.755T= (p.Val252=)
c.866T= (p.Val289=)
12g.112477667T>ACA481887641PTPN11c.870T>A (p.Val290=)
c.756T>A (p.Val252=)
c.867T>A (p.Val289=)
12g.112477667T>CCA481887642PTPN11c.870T>C (p.Val290=)
c.756T>C (p.Val252=)
c.867T>C (p.Val289=)
 dbSNP gnomAD v2 gnomAD v4
12g.112477667T>GCA481887643PTPN11c.870T>G (p.Val290=)
c.756T>G (p.Val252=)
c.867T>G (p.Val289=)
12g.112477667T=CA2063775701PTPN11c.870T= (p.Val290=)
c.756T= (p.Val252=)
c.867T= (p.Val289=)
12g.112477668G>ACA386790508PTPN11c.871G>A (p.Val291Ile)
c.757G>A (p.Val253Ile)
c.868G>A (p.Val290Ile)
 dbSNP
12g.112477668G>CCA386790511PTPN11c.871G>C (p.Val291Leu)
c.757G>C (p.Val253Leu)
c.868G>C (p.Val290Leu)
 dbSNP
12g.112477668G>TCA386790512PTPN11c.871G>T (p.Val291Phe)
c.757G>T (p.Val253Phe)
c.868G>T (p.Val290Phe)
12g.112477669T>ACA386790517PTPN11c.872T>A (p.Val291Asp)
c.758T>A (p.Val253Asp)
c.869T>A (p.Val290Asp)
 dbSNP
12g.112477669T>CCA386790520PTPN11c.872T>C (p.Val291Ala)
c.758T>C (p.Val253Ala)
c.869T>C (p.Val290Ala)
12g.112477669T>GCA386790522PTPN11c.872T>G (p.Val291Gly)
c.758T>G (p.Val253Gly)
c.869T>G (p.Val290Gly)
12g.112477670C>ACA481887644PTPN11c.873C>A (p.Val291=)
c.759C>A (p.Val253=)
c.870C>A (p.Val290=)
12g.112477670C>GCA481887645PTPN11c.873C>G (p.Val291=)
c.759C>G (p.Val253=)
c.870C>G (p.Val290=)
 dbSNP
12g.112477670C>TCA481887646PTPN11c.873C>T (p.Val291=)
c.759C>T (p.Val253=)
c.870C>T (p.Val290=)
 dbSNP
12g.112477671C>ACA386790525PTPN11c.874C>A (p.Leu292Ile)
c.760C>A (p.Leu254Ile)
c.871C>A (p.Leu291Ile)
 dbSNP
12g.112477671C=CA2063775707PTPN11c.874C= (p.Leu292=)
c.760C= (p.Leu254=)
c.871C= (p.Leu291=)
12g.112477671C>GCA386790528PTPN11c.874C>G (p.Leu292Val)
c.760C>G (p.Leu254Val)
c.871C>G (p.Leu291Val)
12g.112477671C>TCA243711914PTPN11c.874C>T (p.Leu292=)
c.760C>T (p.Leu254=)
c.871C>T (p.Leu291=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
12g.112477672T>ACA386790531PTPN11c.875T>A (p.Leu292Gln)
c.761T>A (p.Leu254Gln)
c.872T>A (p.Leu291Gln)
12g.112477672T>CCA386790533PTPN11c.875T>C (p.Leu292Pro)
c.761T>C (p.Leu254Pro)
c.872T>C (p.Leu291Pro)
 gnomAD v4
12g.112477672T>GCA386790534PTPN11c.875T>G (p.Leu292Arg)
c.761T>G (p.Leu254Arg)
c.872T>G (p.Leu291Arg)
12g.112477673A>CCA481887647PTPN11c.876A>C (p.Leu292=)
c.762A>C (p.Leu254=)
c.873A>C (p.Leu291=)
 dbSNP
12g.112477673A>GCA481887648PTPN11c.876A>G (p.Leu292=)
c.762A>G (p.Leu254=)
c.873A>G (p.Leu291=)
 gnomAD v4
12g.112477673A>TCA481887649PTPN11c.876A>T (p.Leu292=)
c.762A>T (p.Leu254=)
c.873A>T (p.Leu291=)
 dbSNP
12g.112477674C>ACA386790543PTPN11c.877C>A (p.His293Asn)
c.763C>A (p.His255Asn)
c.874C>A (p.His292Asn)
 dbSNP
12g.112477674C=CA2063775714PTPN11c.877C= (p.His293=)
c.763C= (p.His255=)
c.874C= (p.His292=)
12g.112477674C>GCA386790539PTPN11c.877C>G (p.His293Asp)
c.763C>G (p.His255Asp)
c.874C>G (p.His292Asp)
 dbSNP
12g.112477674C>TCA386790541PTPN11c.877C>T (p.His293Tyr)
c.763C>T (p.His255Tyr)
c.874C>T (p.His292Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.112477675A>CCA386790547PTPN11c.878A>C (p.His293Pro)
c.764A>C (p.His255Pro)
c.875A>C (p.His292Pro)
12g.112477675A>GCA386790550PTPN11c.878A>G (p.His293Arg)
c.764A>G (p.His255Arg)
c.875A>G (p.His292Arg)
12g.112477675A>TCA386790549PTPN11c.878A>T (p.His293Leu)
c.764A>T (p.His255Leu)
c.875A>T (p.His292Leu)
 dbSNP
12g.112477676C>ACA386790553PTPN11c.879C>A (p.His293Gln)
c.765C>A (p.His255Gln)
c.876C>A (p.His292Gln)
 ClinVar dbSNP gnomAD v4
12g.112477676C=CA2063775718PTPN11c.879C= (p.His293=)
c.765C= (p.His255=)
c.876C= (p.His292=)
12g.112477676C>GCA6798673PTPN11c.879C>G (p.His293Gln)
c.765C>G (p.His255Gln)
c.876C>G (p.His292Gln)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
12g.112477676C>TCA282101PTPN11c.879C>T (p.His293=)
c.765C>T (p.His255=)
c.876C>T (p.His292=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.112477677G>ACA243711916PTPN11c.880G>A (p.Asp294Asn)
c.766G>A (p.Asp256Asn)
c.877G>A (p.Asp293Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.112477677G>CCA386790562PTPN11c.880G>C (p.Asp294His)
c.766G>C (p.Asp256His)
c.877G>C (p.Asp293His)
 dbSNP
12g.112477677G=CA2063775726PTPN11c.880G= (p.Asp294=)
c.766G= (p.Asp256=)
c.877G= (p.Asp293=)
12g.112477677G>TCA243711919PTPN11c.880G>T (p.Asp294Tyr)
c.766G>T (p.Asp256Tyr)
c.877G>T (p.Asp293Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.112477678A=CA2063775731PTPN11c.881A= (p.Asp294=)
c.767A= (p.Asp256=)
c.878A= (p.Asp293=)
12g.112477678A>CCA386790568PTPN11c.881A>C (p.Asp294Ala)
c.767A>C (p.Asp256Ala)
c.878A>C (p.Asp293Ala)
12g.112477678A>GCA6798674PTPN11c.881A>G (p.Asp294Gly)
c.767A>G (p.Asp256Gly)
c.878A>G (p.Asp293Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.112477678A>TCA386790571PTPN11c.881A>T (p.Asp294Val)
c.767A>T (p.Asp256Val)
c.878A>T (p.Asp293Val)
 dbSNP
12g.112477679T>ACA386790577PTPN11c.882T>A (p.Asp294Glu)
c.768T>A (p.Asp256Glu)
c.879T>A (p.Asp293Glu)
12g.112477679T>CCA481887652PTPN11c.882T>C (p.Asp294=)
c.768T>C (p.Asp256=)
c.879T>C (p.Asp293=)
 ClinVar dbSNP gnomAD v4
12g.112477679T>GCA386790574PTPN11c.882T>G (p.Asp294Glu)
c.768T>G (p.Asp256Glu)
c.879T>G (p.Asp293Glu)
 gnomAD v4
12g.112477679T=CA2063775734PTPN11c.882T= (p.Asp294=)
c.768T= (p.Asp256=)
c.879T= (p.Asp293=)
12g.112477680G>ACA386790578PTPN11c.883G>A (p.Gly295Ser)
c.769G>A (p.Gly257Ser)
c.880G>A (p.Gly294Ser)
 dbSNP
12g.112477680G>CCA386790579PTPN11c.883G>C (p.Gly295Arg)
c.769G>C (p.Gly257Arg)
c.880G>C (p.Gly294Arg)
 dbSNP
12g.112477680G>TCA386790580PTPN11c.883G>T (p.Gly295Cys)
c.769G>T (p.Gly257Cys)
c.880G>T (p.Gly294Cys)
12g.112477681G>ACA386790582PTPN11c.884G>A (p.Gly295Asp)
c.770G>A (p.Gly257Asp)
c.881G>A (p.Gly294Asp)
 dbSNP
12g.112477681G>CCA386790583PTPN11c.884G>C (p.Gly295Ala)
c.770G>C (p.Gly257Ala)
c.881G>C (p.Gly294Ala)
 dbSNP
12g.112477681G>TCA386790585PTPN11c.884G>T (p.Gly295Val)
c.770G>T (p.Gly257Val)
c.881G>T (p.Gly294Val)
 dbSNP
12g.112477682T>ACA481887656PTPN11c.885T>A (p.Gly295=)
c.771T>A (p.Gly257=)
c.882T>A (p.Gly294=)
 dbSNP
12g.112477682T>CCA481887657PTPN11c.885T>C (p.Gly295=)
c.771T>C (p.Gly257=)
c.882T>C (p.Gly294=)
12g.112477682T>GCA481887658PTPN11c.885T>G (p.Gly295=)
c.771T>G (p.Gly257=)
c.882T>G (p.Gly294=)
12g.112477683G>ACA386790588PTPN11c.886G>A (p.Asp296Asn)
c.772G>A (p.Asp258Asn)
c.883G>A (p.Asp295Asn)
 dbSNP
12g.112477683G>CCA386790591PTPN11c.886G>C (p.Asp296His)
c.772G>C (p.Asp258His)
c.883G>C (p.Asp295His)
 dbSNP
12g.112477683G>TCA386790590PTPN11c.886G>T (p.Asp296Tyr)
c.772G>T (p.Asp258Tyr)
c.883G>T (p.Asp295Tyr)

Number of alleles fetched