Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112446347T>ACA386776266PTPN11c.86T>A (p.Phe29Tyr)
12g.112446347T>CCA386776267PTPN11c.86T>C (p.Phe29Ser)
12g.112446347T>GCA386776268PTPN11c.86T>G (p.Phe29Cys)
12g.112446348T>ACA386776269PTPN11c.87T>A (p.Phe29Leu)
12g.112446348T>CCA481880966PTPN11c.87T>C (p.Phe29=)
12g.112446348T>GCA386776270PTPN11c.87T>G (p.Phe29Leu)
12g.112446349T>ACA386776271PTPN11c.88T>A (p.Leu30Met)
12g.112446349T>CCA481880969PTPN11c.88T>C (p.Leu30=)
12g.112446349T>GCA386776272PTPN11c.88T>G (p.Leu30Val)
12g.112446350T>ACA386776273PTPN11c.89T>A (p.Leu30Ter)
dbSNP
12g.112446350T>CCA386776274PTPN11c.89T>C (p.Leu30Ser)
12g.112446350T>GCA386776275PTPN11c.89T>G (p.Leu30Trp)
12g.112446351G>ACA481880970PTPN11c.90G>A (p.Leu30=)
12g.112446351G>CCA386776276PTPN11c.90G>C (p.Leu30Phe)
gnomAD v4
12g.112446351G>TCA386776277PTPN11c.90G>T (p.Leu30Phe)
gnomAD v4
12g.112446352G>ACA386776278PTPN11c.91G>A (p.Ala31Thr)
12g.112446352G>CCA386776279PTPN11c.91G>C (p.Ala31Pro)
12g.112446352G>TCA386776280PTPN11c.91G>T (p.Ala31Ser)
ClinVar
12g.112446353C>ACA386776281PTPN11c.92C>A (p.Ala31Glu)
dbSNP
12g.112446353C=CA2063771450PTPN11c.92C= (p.Ala31=)
12g.112446353C>GCA386776282PTPN11c.92C>G (p.Ala31Gly)
ClinVar dbSNP
12g.112446353C>TCA386776283PTPN11c.92C>T (p.Ala31Val)
dbSNP
12g.112446354A>CCA481880971PTPN11c.93A>C (p.Ala31=)
12g.112446354A>GCA481880972PTPN11c.93A>G (p.Ala31=)
12g.112446354A>TCA481880973PTPN11c.93A>T (p.Ala31=)
12g.112446355A>CCA481880974PTPN11c.94A>C (p.Arg32=)
12g.112446355A>GCA386776284PTPN11c.94A>G (p.Arg32Gly)
12g.112446355A>TCA386776285PTPN11c.94A>T (p.Arg32Trp)
12g.112446356G>ACA386776286PTPN11c.95G>A (p.Arg32Lys)
12g.112446356G>CCA386776287PTPN11c.95G>C (p.Arg32Thr)
12g.112446356G>TCA386776288PTPN11c.95G>T (p.Arg32Met)
dbSNP
12g.112446357G>ACA481880975PTPN11c.96G>A (p.Arg32=)
gnomAD v4
12g.112446357G>CCA386776289PTPN11c.96G>C (p.Arg32Ser)
12g.112446357G>TCA386776290PTPN11c.96G>T (p.Arg32Ser)
12g.112446358C>ACA386776291PTPN11c.97C>A (p.Pro33Thr)
12g.112446358C>GCA386776292PTPN11c.97C>G (p.Pro33Ala)
12g.112446358C>TCA386776293PTPN11c.97C>T (p.Pro33Ser)
COSMIC
12g.112446359C>ACA386776294PTPN11c.98C>A (p.Pro33His)
12g.112446359C>GCA386776295PTPN11c.98C>G (p.Pro33Arg)
12g.112446359C>TCA386776296PTPN11c.98C>T (p.Pro33Leu)
COSMIC
12g.112446360T>ACA481880978PTPN11c.99T>A (p.Pro33=)
12g.112446360T>CCA481880979PTPN11c.99T>C (p.Pro33=)
ClinVar dbSNP gnomAD v4
12g.112446360T>GCA481880980PTPN11c.99T>G (p.Pro33=)
12g.112446361A>CCA386776299PTPN11c.100A>C (p.Ser34Arg)
12g.112446361A>GCA386776298PTPN11c.100A>G (p.Ser34Gly)
12g.112446361A>TCA386776297PTPN11c.100A>T (p.Ser34Cys)
12g.112446362G>ACA243707498PTPN11c.101G>A (p.Ser34Asn)
dbSNP gnomAD v4
12g.112446362G>CCA386776300PTPN11c.101G>C (p.Ser34Thr)
12g.112446362G=CA2063771454PTPN11c.101G= (p.Ser34=)
12g.112446362G>TCA386776301PTPN11c.101G>T (p.Ser34Ile)

Number of alleles fetched