Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.71834379G>A | CA377155705 | PSAP | c.167C>T (p.Pro56Leu) | |
10 | g.71834379G>C | CA5547881 | PSAP | c.167C>G (p.Pro56Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834379G= | CA1918891041 | PSAP | c.167C= (p.Pro56=) | |
10 | g.71834379G>T | CA377155708 | PSAP | c.167C>A (p.Pro56Gln) | |
10 | g.71834380G>A | CA209471806 | PSAP | c.166C>T (p.Pro56Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834380G>C | CA377155711 | PSAP | c.166C>G (p.Pro56Ala) | |
10 | g.71834380G= | CA1918891043 | PSAP | c.166C= (p.Pro56=) | |
10 | g.71834380G>T | CA377155713 | PSAP | c.166C>A (p.Pro56Thr) | |
10 | g.71834381C>A | CA377155714 | PSAP | c.165G>T (p.Lys55Asn) | dbSNP gnomAD v4 |
10 | g.71834381C= | CA1918891048 | PSAP | c.165G= (p.Lys55=) | |
10 | g.71834381C>G | CA377155717 | PSAP | c.165G>C (p.Lys55Asn) | |
10 | g.71834381C>T | CA470061819 | PSAP | c.165G>A (p.Lys55=) | gnomAD v4 |
10 | g.71834382T>A | CA377155720 | PSAP | c.164A>T (p.Lys55Met) | |
10 | g.71834382T>C | CA377155721 | PSAP | c.164A>G (p.Lys55Arg) | |
10 | g.71834382T>G | CA377155722 | PSAP | c.164A>C (p.Lys55Thr) | |
10 | g.71834383T>A | CA377155723 | PSAP | c.163A>T (p.Lys55Ter) | |
10 | g.71834383T>C | CA377155724 | PSAP | c.163A>G (p.Lys55Glu) | gnomAD v4 |
10 | g.71834383T>G | CA377155726 | PSAP | c.163A>C (p.Lys55Gln) | gnomAD v4 |
10 | g.71834384G>A | CA470061820 | PSAP | c.162C>T (p.Asn54=) | |
10 | g.71834384G>C | CA377155729 | PSAP | c.162C>G (p.Asn54Lys) | |
10 | g.71834384G>T | CA377155727 | PSAP | c.162C>A (p.Asn54Lys) | |
10 | g.71834385T>A | CA377155732 | PSAP | c.161A>T (p.Asn54Ile) | |
10 | g.71834385T>C | CA5547882 | PSAP | c.161A>G (p.Asn54Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
10 | g.71834385T>G | CA377155736 | PSAP | c.161A>C (p.Asn54Thr) | |
10 | g.71834385T= | CA1918891051 | PSAP | c.161A= (p.Asn54=) | |
10 | g.71834386T>A | CA377155750 | PSAP | c.160A>T (p.Asn54Tyr) | |
10 | g.71834386T>C | CA377155752 | PSAP | c.160A>G (p.Asn54Asp) | |
10 | g.71834386T>G | CA377155759 | PSAP | c.160A>C (p.Asn54His) | |
10 | g.71834387C>A | CA377155772 | PSAP | c.159G>T (p.Trp53Cys) | |
10 | g.71834387C>G | CA377155764 | PSAP | c.159G>C (p.Trp53Cys) | |
10 | g.71834387C>T | CA377155766 | PSAP | c.159G>A (p.Trp53Ter) | |
10 | g.71834388C>A | CA377155773 | PSAP | c.158G>T (p.Trp53Leu) | |
10 | g.71834388C>G | CA377155774 | PSAP | c.158G>C (p.Trp53Ser) | |
10 | g.71834388C>T | CA377155775 | PSAP | c.158G>A (p.Trp53Ter) | ClinVar |
10 | g.71834389A>C | CA377155776 | PSAP | c.157T>G (p.Trp53Gly) | |
10 | g.71834389A>G | CA377155777 | PSAP | c.157T>C (p.Trp53Arg) | |
10 | g.71834389A>T | CA377155779 | PSAP | c.157T>A (p.Trp53Arg) | |
10 | g.71834391dup | CA2609589036 | PSAP | c.157dup (p.Trp53LeufsTer23) | gnomAD v4 |
10 | g.71834390A>C | CA470061821 | PSAP | c.156T>G (p.Val52=) | |
10 | g.71834390A>G | CA470061823 | PSAP | c.156T>C (p.Val52=) | gnomAD v4 |
10 | g.71834390A>T | CA470061822 | PSAP | c.156T>A (p.Val52=) | |
10 | g.71834391A>C | CA377155783 | PSAP | c.155T>G (p.Val52Gly) | |
10 | g.71834391A>G | CA377155784 | PSAP | c.155T>C (p.Val52Ala) | |
10 | g.71834391A>T | CA377155787 | PSAP | c.155T>A (p.Val52Asp) | |
10 | g.71834392C>A | CA377155788 | PSAP | c.154G>T (p.Val52Phe) | |
10 | g.71834392C= | CA1918891053 | PSAP | c.154G= (p.Val52=) | |
10 | g.71834392C>G | CA377155789 | PSAP | c.154G>C (p.Val52Leu) | |
10 | g.71834392C>T | CA5547883 | PSAP | c.154G>A (p.Val52Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
10 | g.71834393G>A | CA5547884 | PSAP | c.153C>T (p.Thr51=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834393G>C | CA470061824 | PSAP | c.153C>G (p.Thr51=) | ClinVar gnomAD v4 |