Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112450335C>TCA261555PTPN11c.155C>T (p.Thr52Ile)
c.152C>T (p.Thr51Ile)
ClinVar dbSNP gnomAD v4 COSMIC
12g.112450335C>GCA386777440PTPN11c.155C>G (p.Thr52Ser)
c.152C>G (p.Thr51Ser)
dbSNP COSMIC
12g.112450335C>ACA386777437PTPN11c.155C>A (p.Thr52Asn)
c.152C>A (p.Thr51Asn)
dbSNP

Number of alleles fetched