Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.71834363G>A | CA5547878 | PSAP | c.174+9C>T (n.174+9C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834363G= | CA1918891022 | PSAP | c.174+9C= (n.174+9C=) | |
10 | g.71834364G>A | CA2609589006 | PSAP | c.174+8C>T (n.174+8C>T) | gnomAD v4 |
10 | g.71834367C= | CA1918891024 | PSAP | c.174+5G= (n.174+5G=) | |
10 | g.71834367C>T | CA5547879 | PSAP | c.174+5G>A (n.174+5G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834370A= | CA1918891025 | PSAP | c.174+2T= (n.174+2T=) | |
10 | g.71834370A>C | CA377155679 | PSAP | c.174+2T>G (n.174+2T>G) | |
10 | g.71834370A>G | CA377155681 | PSAP | c.174+2T>C (n.174+2T>C) | dbSNP |
10 | g.71834370A>T | CA377155683 | PSAP | c.174+2T>A (n.174+2T>A) | |
10 | g.71834371C>A | CA377155684 | PSAP | c.174+1G>T (n.174+1G>T) | |
10 | g.71834371C= | CA1918891026 | PSAP | c.174+1G= (n.174+1G=) | |
10 | g.71834371C>G | CA209471778 | PSAP | c.174+1G>C (n.174+1G>C) | dbSNP |
10 | g.71834371C>T | CA209471783 | PSAP | c.174+1G>A (n.174+1G>A) | dbSNP |
10 | g.71834372C>A | CA470061812 | PSAP | c.174G>T (p.Val58=) | |
10 | g.71834372C>G | CA470061811 | PSAP | c.174G>C (p.Val58=) | |
10 | g.71834372C>T | CA470061809 | PSAP | c.174G>A (p.Val58=) | |
10 | g.71834373A>C | CA377155685 | PSAP | c.173T>G (p.Val58Gly) | |
10 | g.71834373A>G | CA377155687 | PSAP | c.173T>C (p.Val58Ala) | |
10 | g.71834373A>T | CA377155689 | PSAP | c.173T>A (p.Val58Glu) | |
10 | g.71834374C>A | CA377155692 | PSAP | c.172G>T (p.Val58Leu) | |
10 | g.71834374C>G | CA377155690 | PSAP | c.172G>C (p.Val58Leu) | |
10 | g.71834374C>T | CA377155691 | PSAP | c.172G>A (p.Val58Met) | |
10 | g.71834375T>A | CA470061813 | PSAP | c.171A>T (p.Thr57=) | |
10 | g.71834375T>C | CA470061814 | PSAP | c.171A>G (p.Thr57=) | gnomAD v4 |
10 | g.71834375T>G | CA470061815 | PSAP | c.171A>C (p.Thr57=) | |
10 | g.71834376G>A | CA377155693 | PSAP | c.170C>T (p.Thr57Ile) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.71834376G>C | CA377155694 | PSAP | c.170C>G (p.Thr57Arg) | dbSNP gnomAD v3 gnomAD v4 |
10 | g.71834376G= | CA1918891028 | PSAP | c.170C= (p.Thr57=) | |
10 | g.71834376G>T | CA377155696 | PSAP | c.170C>A (p.Thr57Lys) | |
10 | g.71834377T>A | CA5547880 | PSAP | c.169A>T (p.Thr57Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834377T>C | CA377155701 | PSAP | c.169A>G (p.Thr57Ala) | dbSNP gnomAD v4 |
10 | g.71834377T>G | CA377155704 | PSAP | c.169A>C (p.Thr57Pro) | |
10 | g.71834377T= | CA1918891033 | PSAP | c.169A= (p.Thr57=) | |
10 | g.71834378T>A | CA470061816 | PSAP | c.168A>T (p.Pro56=) | |
10 | g.71834378T>C | CA470061817 | PSAP | c.168A>G (p.Pro56=) | gnomAD v4 |
10 | g.71834378T>G | CA470061818 | PSAP | c.168A>C (p.Pro56=) | ClinVar dbSNP gnomAD v4 |
10 | g.71834378T= | CA1918891036 | PSAP | c.168A= (p.Pro56=) | |
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) |