Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112446376G>A | CA10603228 | PTPN11 | c.115G>A (p.Gly39Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
12 | g.112446376G>C | CA386776333 | PTPN11 | c.115G>C (p.Gly39Arg) | dbSNP gnomAD v4 |
12 | g.112446376G= | CA2063771478 | PTPN11 | c.115G= (p.Gly39=) | |
12 | g.112446376G>T | CA386776334 | PTPN11 | c.115G>T (p.Gly39Ter) | |
12 | g.112446377G>A | CA386776335 | PTPN11 | c.116G>A (p.Gly39Glu) | |
12 | g.112446377G>C | CA386776336 | PTPN11 | c.116G>C (p.Gly39Ala) | |
12 | g.112446377G>T | CA386776337 | PTPN11 | c.116G>T (p.Gly39Val) | |
12 | g.112446378A= | CA2063771484 | PTPN11 | c.117A= (p.Gly39=) | |
12 | g.112446378A>C | CA6798514 | PTPN11 | c.117A>C (p.Gly39=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.112446378A>G | CA481881018 | PTPN11 | c.117A>G (p.Gly39=) | |
12 | g.112446378A>T | CA481881017 | PTPN11 | c.117A>T (p.Gly39=) | |
12 | g.112446379G>A | CA386776338 | PTPN11 | c.118G>A (p.Asp40Asn) | |
12 | g.112446379G>C | CA386776339 | PTPN11 | c.118G>C (p.Asp40His) | |
12 | g.112446379G>T | CA386776340 | PTPN11 | c.118G>T (p.Asp40Tyr) | |
12 | g.112446380A= | CA2063771488 | PTPN11 | c.119A= (p.Asp40=) | |
12 | g.112446380A>C | CA386776342 | PTPN11 | c.119A>C (p.Asp40Ala) | |
12 | g.112446380A>G | CA134635 | PTPN11 | c.119A>G (p.Asp40Gly) | ClinVar dbSNP |
12 | g.112446380A>T | CA386776341 | PTPN11 | c.119A>T (p.Asp40Val) | |
12 | g.112446381C>A | CA386776343 | PTPN11 | c.120C>A (p.Asp40Glu) | |
12 | g.112446381C>G | CA386776344 | PTPN11 | c.120C>G (p.Asp40Glu) | |
12 | g.112446381C>T | CA481881031 | PTPN11 | c.120C>T (p.Asp40=) | |
12 | g.112446382T>A | CA386776345 | PTPN11 | c.121T>A (p.Phe41Ile) | |
12 | g.112446382T>C | CA386776346 | PTPN11 | c.121T>C (p.Phe41Leu) | |
12 | g.112446382T>G | CA386776347 | PTPN11 | c.121T>G (p.Phe41Val) | |
12 | g.112446383T>A | CA386776348 | PTPN11 | c.122T>A (p.Phe41Tyr) | |
12 | g.112446383T>C | CA386776349 | PTPN11 | c.122T>C (p.Phe41Ser) | dbSNP |
12 | g.112446383T>G | CA386776350 | PTPN11 | c.122T>G (p.Phe41Cys) | |
12 | g.112446384C>A | CA386776351 | PTPN11 | c.123C>A (p.Phe41Leu) | |
12 | g.112446384C= | CA2063771517 | PTPN11 | c.123C= (p.Phe41=) | |
12 | g.112446384C>G | CA386776352 | PTPN11 | c.123C>G (p.Phe41Leu) | dbSNP |
12 | g.112446384C>T | CA481881046 | PTPN11 | c.123C>T (p.Phe41=) | dbSNP |
12 | g.112446385A= | CA2063771525 | PTPN11 | c.124A= (p.Thr42=) | |
12 | g.112446385A>C | CA386776353 | PTPN11 | c.124A>C (p.Thr42Pro) | |
12 | g.112446385A>G | CA235307 | PTPN11 | c.124A>G (p.Thr42Ala) | ClinVar dbSNP COSMIC |
12 | g.112446385A>T | CA386776354 | PTPN11 | c.124A>T (p.Thr42Ser) | |
12 | g.112446386C>A | CA386776357 | PTPN11 | c.125C>A (p.Thr42Lys) | |
12 | g.112446386C>G | CA386776355 | PTPN11 | c.125C>G (p.Thr42Arg) | |
12 | g.112446386C>T | CA386776356 | PTPN11 | c.125C>T (p.Thr42Ile) | |
12 | g.112446387A= | CA2063771532 | PTPN11 | c.126A= (p.Thr42=) | |
12 | g.112446387A>C | CA481881061 | PTPN11 | c.126A>C (p.Thr42=) | |
12 | g.112446387A>G | CA481881064 | PTPN11 | c.126A>G (p.Thr42=) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.112446387A>T | CA481881066 | PTPN11 | c.126A>T (p.Thr42=) | |
12 | g.112446388C>A | CA386776358 | PTPN11 | c.127C>A (p.Leu43Ile) | dbSNP |
12 | g.112446388C= | CA2063771539 | PTPN11 | c.127C= (p.Leu43=) | |
12 | g.112446388C>G | CA386776359 | PTPN11 | c.127C>G (p.Leu43Val) | ClinVar dbSNP gnomAD v4 |
12 | g.112446388C>T | CA386776360 | PTPN11 | c.127C>T (p.Leu43Phe) | ClinVar dbSNP |
12 | g.112446389T>A | CA386776361 | PTPN11 | c.128T>A (p.Leu43His) | |
12 | g.112446389T>C | CA386776362 | PTPN11 | c.128T>C (p.Leu43Pro) | |
12 | g.112446389T>G | CA386776363 | PTPN11 | c.128T>G (p.Leu43Arg) | |
12 | g.112446390T>A | CA481881077 | PTPN11 | c.129T>A (p.Leu43=) |