Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.160127585A>C | CA343237128 | ATP1A2 | c.782A>C (p.Asp261Ala) n.885A>C | |
1 | g.160127585A>G | CA343237134 | ATP1A2 | c.782A>G (p.Asp261Gly) n.885A>G | ClinVar COSMIC |
1 | g.160127585A>T | CA343237141 | ATP1A2 | c.782A>T (p.Asp261Val) n.885A>T | |
1 | g.160127586C>A | CA343237158 | ATP1A2 | c.783C>A (p.Asp261Glu) n.886C>A | |
1 | g.160127586C>G | CA343237151 | ATP1A2 | c.783C>G (p.Asp261Glu) n.886C>G | |
1 | g.160127586C>T | CA421599439 | ATP1A2 | c.783C>T (p.Asp261=) n.886C>T | |
1 | g.160127587C>A | CA421599441 | ATP1A2 | c.784C>A (p.Arg262=) n.887C>A | |
1 | g.160127587C= | CA1148722163 | ATP1A2 | c.784C= (p.Arg262=) n.887C= | |
1 | g.160127587C>G | CA343237165 | ATP1A2 | c.784C>G (p.Arg262Gly) n.887C>G | dbSNP |
1 | g.160127587C>T | CA1194288 | ATP1A2 | c.784C>T (p.Arg262Trp) n.887C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.160127588G>A | CA1194289 | ATP1A2 | c.785G>A (p.Arg262Gln) n.888G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.160127588G>C | CA343237175 | ATP1A2 | c.785G>C (p.Arg262Pro) n.888G>C | |
1 | g.160127588G= | CA1202191851 | ATP1A2 | c.785G= (p.Arg262=) n.888G= | |
1 | g.160127588G>T | CA343237177 | ATP1A2 | c.785G>T (p.Arg262Leu) n.888G>T | |
1 | g.160127589G>A | CA421599448 | ATP1A2 | c.786G>A (p.Arg262=) n.889G>A | |
1 | g.160127589G>C | CA421599451 | ATP1A2 | c.786G>C (p.Arg262=) n.889G>C | |
1 | g.160127589G>T | CA421599449 | ATP1A2 | c.786G>T (p.Arg262=) n.889G>T | |
1 | g.160127590A>C | CA343237181 | ATP1A2 | c.787A>C (p.Thr263Pro) n.890A>C | |
1 | g.160127590A>G | CA343237183 | ATP1A2 | c.787A>G (p.Thr263Ala) n.890A>G | |
1 | g.160127590A>T | CA343237200 | ATP1A2 | c.787A>T (p.Thr263Ser) n.890A>T | |
1 | g.160127591C>A | CA1194290 | ATP1A2 | c.788C>A (p.Thr263Lys) n.891C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.160127591C= | CA1202191852 | ATP1A2 | c.788C= (p.Thr263=) n.891C= | |
1 | g.160127591C>G | CA343237211 | ATP1A2 | c.788C>G (p.Thr263Arg) n.891C>G | |
1 | g.160127591C>T | CA343237213 | ATP1A2 | c.788C>T (p.Thr263Met) n.891C>T | ClinVar dbSNP gnomAD v4 |
1 | g.160127592G>A | CA1194291 | ATP1A2 | c.789G>A (p.Thr263=) n.892G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.160127592G>C | CA1194292 | ATP1A2 | c.789G>C (p.Thr263=) n.892G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.160127592G= | CA1149050296 | ATP1A2 | c.789G= (p.Thr263=) n.892G= | |
1 | g.160127592G>T | CA421599458 | ATP1A2 | c.789G>T (p.Thr263=) n.892G>T | |
1 | g.160127593G>A | CA343237225 | ATP1A2 | c.790G>A (p.Val264Met) n.893G>A | COSMIC |
1 | g.160127593G>C | CA343237224 | ATP1A2 | c.790G>C (p.Val264Leu) n.893G>C | |
1 | g.160127593G>T | CA343237221 | ATP1A2 | c.790G>T (p.Val264Leu) n.893G>T | |
1 | g.160127594T>A | CA343237226 | ATP1A2 | c.791T>A (p.Val264Glu) n.894T>A | |
1 | g.160127594T>C | CA343237227 | ATP1A2 | c.791T>C (p.Val264Ala) n.894T>C | gnomAD v4 |
1 | g.160127594T>G | CA343237229 | ATP1A2 | c.791T>G (p.Val264Gly) n.894T>G | |
1 | g.160127595G>A | CA421599464 | ATP1A2 | c.792G>A (p.Val264=) n.895G>A | |
1 | g.160127595G>C | CA421599466 | ATP1A2 | c.792G>C (p.Val264=) n.895G>C | |
1 | g.160127595G>T | CA421599468 | ATP1A2 | c.792G>T (p.Val264=) n.895G>T | |
1 | g.160127596A>C | CA343237232 | ATP1A2 | c.793A>C (p.Met265Leu) n.896A>C | |
1 | g.160127596A>G | CA343237235 | ATP1A2 | c.793A>G (p.Met265Val) n.896A>G | |
1 | g.160127596A>T | CA343237236 | ATP1A2 | c.793A>T (p.Met265Leu) n.896A>T | |
1 | g.160127597T>A | CA343237239 | ATP1A2 | c.794T>A (p.Met265Lys) n.897T>A | |
1 | g.160127597T>C | CA343237241 | ATP1A2 | c.794T>C (p.Met265Thr) n.897T>C | ClinVar dbSNP |
1 | g.160127597T>G | CA343237243 | ATP1A2 | c.794T>G (p.Met265Arg) n.897T>G | |
1 | g.160127597T= | CA1202191853 | ATP1A2 | c.794T= (p.Met265=) n.897T= | |
1 | g.160127598G>A | CA343237245 | ATP1A2 | c.795G>A (p.Met265Ile) n.898G>A | |
1 | g.160127598G>C | CA343237246 | ATP1A2 | c.795G>C (p.Met265Ile) n.898G>C | |
1 | g.160127598G>T | CA343237254 | ATP1A2 | c.795G>T (p.Met265Ile) n.898G>T | |
1 | g.160127599G>A | CA343237263 | ATP1A2 | c.796G>A (p.Gly266Ser) n.899G>A | |
1 | g.160127599G>C | CA343237270 | ATP1A2 | c.796G>C (p.Gly266Arg) n.899G>C | |
1 | g.160127599G>T | CA343237260 | ATP1A2 | c.796G>T (p.Gly266Cys) n.899G>T |