Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49612409G>A | CA3847786 | RHAG | c.933C>T (p.Tyr311=) n.623C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612409G>C | CA3847787 | RHAG | c.933C>G (p.Tyr311Ter) n.623C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612409G= | CA1627468957 | RHAG | c.933C= (p.Tyr311=) n.623C= | |
6 | g.49612409G>T | CA364398136 | RHAG | c.933C>A (p.Tyr311Ter) n.623C>A | |
6 | g.49612410T>A | CA364398139 | RHAG | c.932A>T (p.Tyr311Phe) n.622A>T | gnomAD v4 |
6 | g.49612410T>C | CA364398140 | RHAG | c.932A>G (p.Tyr311Cys) n.622A>G | gnomAD v4 |
6 | g.49612410T>G | CA364398142 | RHAG | c.932A>C (p.Tyr311Ser) n.622A>C | |
6 | g.49612411A= | CA1627468962 | RHAG | c.931T= (p.Tyr311=) n.621T= | |
6 | g.49612411A>C | CA364398145 | RHAG | c.931T>G (p.Tyr311Asp) n.621T>G | |
6 | g.49612411A>G | CA364398146 | RHAG | c.931T>C (p.Tyr311His) n.621T>C | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612411A>T | CA364398148 | RHAG | c.931T>A (p.Tyr311Asn) n.621T>A | |
6 | g.49612412T>A | CA450401473 | RHAG | c.930A>T (p.Gly310=) n.620A>T | |
6 | g.49612412T>C | CA450401476 | RHAG | c.930A>G (p.Gly310=) n.620A>G | |
6 | g.49612412T>G | CA450401477 | RHAG | c.930A>C (p.Gly310=) n.620A>C | |
6 | g.49612413C>A | CA364398149 | RHAG | c.929G>T (p.Gly310Val) n.619G>T | gnomAD v4 |
6 | g.49612413C>G | CA364398153 | RHAG | c.929G>C (p.Gly310Ala) n.619G>C | |
6 | g.49612413C>T | CA364398151 | RHAG | c.929G>A (p.Gly310Glu) n.619G>A | |
6 | g.49612414C>A | CA364398155 | RHAG | c.928G>T (p.Gly310Ter) n.618G>T | |
6 | g.49612414C>G | CA364398156 | RHAG | c.928G>C (p.Gly310Arg) n.618G>C | |
6 | g.49612414C>T | CA364398157 | RHAG | c.928G>A (p.Gly310Arg) n.618G>A | |
6 | g.49612415A= | CA1627468965 | RHAG | c.927T= (p.Leu309=) n.617T= | |
6 | g.49612415A>C | CA450401478 | RHAG | c.927T>G (p.Leu309=) n.617T>G | |
6 | g.49612415A>G | CA3847788 | RHAG | c.927T>C (p.Leu309=) n.617T>C | dbSNP ExAC gnomAD v2 |
6 | g.49612415A>T | CA450401480 | RHAG | c.927T>A (p.Leu309=) n.617T>A | |
6 | g.49612416A>C | CA364398158 | RHAG | c.926T>G (p.Leu309Arg) n.616T>G | |
6 | g.49612416A>G | CA364398159 | RHAG | c.926T>C (p.Leu309Pro) n.616T>C | |
6 | g.49612416A>T | CA364398161 | RHAG | c.926T>A (p.Leu309His) n.616T>A | |
6 | g.49612417G>A | CA3847789 | RHAG | c.925C>T (p.Leu309Phe) n.615C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612417G>C | CA364398163 | RHAG | c.925C>G (p.Leu309Val) n.615C>G | |
6 | g.49612417G= | CA1627468971 | RHAG | c.925C= (p.Leu309=) n.615C= | |
6 | g.49612417G>T | CA364398164 | RHAG | c.925C>A (p.Leu309Ile) n.615C>A | |
6 | g.49612418C>A | CA450401481 | RHAG | c.924G>T (p.Val308=) n.614G>T | |
6 | g.49612418C>G | CA450401482 | RHAG | c.924G>C (p.Val308=) n.614G>C | |
6 | g.49612418C>T | CA450401484 | RHAG | c.924G>A (p.Val308=) n.614G>A | |
6 | g.49612419A>C | CA364398167 | RHAG | c.923T>G (p.Val308Gly) n.613T>G | |
6 | g.49612419A>G | CA364398170 | RHAG | c.923T>C (p.Val308Ala) n.613T>C | |
6 | g.49612419A>T | CA364398172 | RHAG | c.923T>A (p.Val308Glu) n.613T>A | |
6 | g.49612420C>A | CA364398177 | RHAG | c.922G>T (p.Val308Leu) n.612G>T | |
6 | g.49612420C>G | CA364398173 | RHAG | c.922G>C (p.Val308Leu) n.612G>C | |
6 | g.49612420C>T | CA364398175 | RHAG | c.922G>A (p.Val308Met) n.612G>A | |
6 | g.49612421A= | CA1627468974 | RHAG | c.921T= (p.Ser307=) n.611T= | |
6 | g.49612421A>C | CA450401490 | RHAG | c.921T>G (p.Ser307=) n.611T>G | |
6 | g.49612421A>G | CA450401489 | RHAG | c.921T>C (p.Ser307=) n.611T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612421A>T | CA450401488 | RHAG | c.921T>A (p.Ser307=) n.611T>A | |
6 | g.49612422G>A | CA364398180 | RHAG | c.920C>T (p.Ser307Phe) n.610C>T | ClinVar |
6 | g.49612422G>C | CA3847790 | RHAG | c.920C>G (p.Ser307Cys) n.610C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612422G= | CA1627468981 | RHAG | c.920C= (p.Ser307=) n.610C= | |
6 | g.49612422G>T | CA364398183 | RHAG | c.920C>A (p.Ser307Tyr) n.610C>A | |
6 | g.49612423A>C | CA364398186 | RHAG | c.919T>G (p.Ser307Ala) n.609T>G | |
6 | g.49612423A>G | CA364398189 | RHAG | c.919T>C (p.Ser307Pro) n.609T>C | |
6 | g.49612423A>T | CA364398191 | RHAG | c.919T>A (p.Ser307Thr) n.609T>A | |
6 | g.49612424G>A | CA450401498 | RHAG | c.918C>T (p.Val306=) n.608C>T | COSMIC |
6 | g.49612424G>C | CA450401500 | RHAG | c.918C>G (p.Val306=) n.608C>G | |
6 | g.49612424G>T | CA450401502 | RHAG | c.918C>A (p.Val306=) n.608C>A | |
6 | g.49612425A>C | CA364398192 | RHAG | c.917T>G (p.Val306Gly) n.607T>G | |
6 | g.49612425A>G | CA364398194 | RHAG | c.917T>C (p.Val306Ala) n.607T>C | |
6 | g.49612425A>T | CA364398197 | RHAG | c.917T>A (p.Val306Asp) n.607T>A | |
6 | g.49612426C>A | CA364398200 | RHAG | c.916G>T (p.Val306Phe) n.606G>T | |
6 | g.49612426C>G | CA364398201 | RHAG | c.916G>C (p.Val306Leu) n.606G>C | |
6 | g.49612426C>T | CA364398203 | RHAG | c.916G>A (p.Val306Ile) n.606G>A | COSMIC |
6 | g.49612427C>A | CA364398207 | RHAG | c.915G>T (p.Met305Ile) n.605G>T | |
6 | g.49612427C>G | CA364398212 | RHAG | c.915G>C (p.Met305Ile) n.605G>C | |
6 | g.49612427C>T | CA364398209 | RHAG | c.915G>A (p.Met305Ile) n.605G>A | |
6 | g.49612428A= | CA1627468986 | RHAG | c.914T= (p.Met305=) n.604T= | |
6 | g.49612428A>C | CA364398214 | RHAG | c.914T>G (p.Met305Arg) n.604T>G | |
6 | g.49612428A>G | CA3847791 | RHAG | c.914T>C (p.Met305Thr) n.604T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612428A>T | CA364398216 | RHAG | c.914T>A (p.Met305Lys) n.604T>A | |
6 | g.49612429T>A | CA364398218 | RHAG | c.913A>T (p.Met305Leu) n.603A>T | |
6 | g.49612429T>C | CA364398221 | RHAG | c.913A>G (p.Met305Val) n.603A>G | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612429T>G | CA364398222 | RHAG | c.913A>C (p.Met305Leu) n.603A>C | |
6 | g.49612429T= | CA1627469000 | RHAG | c.913A= (p.Met305=) n.603A= | |
6 | g.49612430T>A | CA450401508 | RHAG | c.912A>T (p.Gly304=) n.602A>T | |
6 | g.49612430T>C | CA450401509 | RHAG | c.912A>G (p.Gly304=) n.602A>G | |
6 | g.49612430T>G | CA450401510 | RHAG | c.912A>C (p.Gly304=) n.602A>C | |
6 | g.49612431C>A | CA364398225 | RHAG | c.911G>T (p.Gly304Val) n.601G>T | |
6 | g.49612431C>G | CA364398227 | RHAG | c.911G>C (p.Gly304Ala) n.601G>C | |
6 | g.49612431C>T | CA364398228 | RHAG | c.911G>A (p.Gly304Glu) n.601G>A | ClinVar |
6 | g.49612432C>A | CA364398231 | RHAG | c.910G>T (p.Gly304Ter) n.600G>T | |
6 | g.49612432C>G | CA364398233 | RHAG | c.910G>C (p.Gly304Arg) n.600G>C | |
6 | g.49612432C>T | CA364398234 | RHAG | c.910G>A (p.Gly304Arg) n.600G>A | |
6 | g.49612433T>A | CA450401512 | RHAG | c.909A>T (p.Ala303=) n.599A>T | |
6 | g.49612433T>C | CA450401514 | RHAG | c.909A>G (p.Ala303=) n.599A>G | gnomAD v4 |
6 | g.49612433T>G | CA450401513 | RHAG | c.909A>C (p.Ala303=) n.599A>C | |
6 | g.49612434G>A | CA364398237 | RHAG | c.908C>T (p.Ala303Val) n.598C>T | |
6 | g.49612434G>C | CA364398238 | RHAG | c.908C>G (p.Ala303Gly) n.598C>G | |
6 | g.49612434G>T | CA364398240 | RHAG | c.908C>A (p.Ala303Glu) n.598C>A | |
6 | g.49612435C>A | CA364398246 | RHAG | c.907G>T (p.Ala303Ser) n.597G>T | |
6 | g.49612435C>G | CA364398243 | RHAG | c.907G>C (p.Ala303Pro) n.597G>C | |
6 | g.49612435C>T | CA364398244 | RHAG | c.907G>A (p.Ala303Thr) n.597G>A | |
6 | g.49612436A= | CA1627469007 | RHAG | c.906T= (p.Ile302=) n.596T= | |
6 | g.49612436A>C | CA364398248 | RHAG | c.906T>G (p.Ile302Met) n.596T>G | |
6 | g.49612436A>G | CA3847792 | RHAG | c.906T>C (p.Ile302=) n.596T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612436A>T | CA450401515 | RHAG | c.906T>A (p.Ile302=) n.596T>A | |
6 | g.49612437A= | CA1627469014 | RHAG | c.905T= (p.Ile302=) n.595T= | |
6 | g.49612437A>C | CA364398252 | RHAG | c.905T>G (p.Ile302Ser) n.595T>G | |
6 | g.49612437A>G | CA3847793 | RHAG | c.905T>C (p.Ile302Thr) n.595T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612437A>T | CA364398266 | RHAG | c.905T>A (p.Ile302Asn) n.595T>A | |
6 | g.49612438T>A | CA364398269 | RHAG | c.904A>T (p.Ile302Phe) n.594A>T | |
6 | g.49612438T>C | CA138843615 | RHAG | c.904A>G (p.Ile302Val) n.594A>G | dbSNP |
6 | g.49612438T>G | CA364398272 | RHAG | c.904A>C (p.Ile302Leu) n.594A>C | |
6 | g.49612438T= | CA1627469022 | RHAG | c.904A= (p.Ile302=) n.594A= | |
6 | g.49612439G>A | CA450401516 | RHAG | c.903C>T (p.Ser301=) n.593C>T | |
6 | g.49612439G>C | CA364398276 | RHAG | c.903C>G (p.Ser301Arg) n.593C>G | |
6 | g.49612439G>T | CA364398279 | RHAG | c.903C>A (p.Ser301Arg) n.593C>A | |
6 | g.49612440C>A | CA364398288 | RHAG | c.902G>T (p.Ser301Ile) n.592G>T | |
6 | g.49612440C>G | CA364398286 | RHAG | c.902G>C (p.Ser301Thr) n.592G>C | |
6 | g.49612440C>T | CA364398283 | RHAG | c.902G>A (p.Ser301Asn) n.592G>A | gnomAD v4 |
6 | g.49612441T>A | CA364398290 | RHAG | c.901A>T (p.Ser301Cys) n.591A>T | |
6 | g.49612441T>C | CA364398293 | RHAG | c.901A>G (p.Ser301Gly) n.591A>G | gnomAD v4 |
6 | g.49612441T>G | CA364398296 | RHAG | c.901A>C (p.Ser301Arg) n.591A>C | |
6 | g.49612442C>A | CA450401522 | RHAG | c.900G>T (p.Gly300=) n.590G>T | |
6 | g.49612442C= | CA1627469027 | RHAG | c.900G= (p.Gly300=) n.590G= | |
6 | g.49612442C>G | CA450401519 | RHAG | c.900G>C (p.Gly300=) n.590G>C | |
6 | g.49612442C>T | CA450401521 | RHAG | c.900G>A (p.Gly300=) n.590G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612443C>A | CA364398299 | RHAG | c.899G>T (p.Gly300Val) n.589G>T | |
6 | g.49612443C>G | CA364398303 | RHAG | c.899G>C (p.Gly300Ala) n.589G>C | |
6 | g.49612443C>T | CA364398304 | RHAG | c.899G>A (p.Gly300Glu) n.589G>A | ClinVar gnomAD v4 |
6 | g.49612444C>A | CA364398309 | RHAG | c.898G>T (p.Gly300Trp) n.588G>T | |
6 | g.49612444C>G | CA364398306 | RHAG | c.898G>C (p.Gly300Arg) n.588G>C | |
6 | g.49612444C>T | CA364398307 | RHAG | c.898G>A (p.Gly300Arg) n.588G>A | gnomAD v4 |
6 | g.49612445A= | CA1627469032 | RHAG | c.897T= (p.Ile299=) n.587T= | |
6 | g.49612445A>C | CA364398311 | RHAG | c.897T>G (p.Ile299Met) n.587T>G | |
6 | g.49612445A>G | CA138843619 | RHAG | c.897T>C (p.Ile299=) n.587T>C | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49612445A>T | CA450401524 | RHAG | c.897T>A (p.Ile299=) n.587T>A | |
6 | g.49612446A= | CA1627469038 | RHAG | c.896T= (p.Ile299=) n.586T= | |
6 | g.49612446A>C | CA364398314 | RHAG | c.896T>G (p.Ile299Ser) n.586T>G | |
6 | g.49612446A>G | CA138843625 | RHAG | c.896T>C (p.Ile299Thr) n.586T>C | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49612446A>T | CA364398319 | RHAG | c.896T>A (p.Ile299Asn) n.586T>A | |
6 | g.49612447T>A | CA364398321 | RHAG | c.895A>T (p.Ile299Phe) n.585A>T | |
6 | g.49612447T>C | CA364398328 | RHAG | c.895A>G (p.Ile299Val) n.585A>G | |
6 | g.49612447T>G | CA364398327 | RHAG | c.895A>C (p.Ile299Leu) n.585A>C | |
6 | g.49612448A= | CA1627469047 | RHAG | c.894T= (p.Ile298=) n.584T= | |
6 | g.49612448A>C | CA3847794 | RHAG | c.894T>G (p.Ile298Met) n.584T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612448A>G | CA450401525 | RHAG | c.894T>C (p.Ile298=) n.584T>C | |
6 | g.49612448A>T | CA450401526 | RHAG | c.894T>A (p.Ile298=) n.584T>A | |
6 | g.49612449A>C | CA364398329 | RHAG | c.893T>G (p.Ile298Ser) n.583T>G | |
6 | g.49612449A>G | CA364398330 | RHAG | c.893T>C (p.Ile298Thr) n.583T>C | |
6 | g.49612449A>T | CA364398331 | RHAG | c.893T>A (p.Ile298Asn) n.583T>A | |
6 | g.49612450T>A | CA364398333 | RHAG | c.892A>T (p.Ile298Phe) n.582A>T | |
6 | g.49612450T>C | CA364398334 | RHAG | c.892A>G (p.Ile298Val) n.582A>G | |
6 | g.49612450T>G | CA364398335 | RHAG | c.892A>C (p.Ile298Leu) n.582A>C | |
6 | g.49612451C>A | CA364398347 | RHAG | c.891G>T (p.Met297Ile) n.581G>T | |
6 | g.49612451C>G | CA364398349 | RHAG | c.891G>C (p.Met297Ile) n.581G>C | |
6 | g.49612451C>T | CA364398351 | RHAG | c.891G>A (p.Met297Ile) n.581G>A | |
6 | g.49612452A>C | CA364398359 | RHAG | c.890T>G (p.Met297Arg) n.580T>G | |
6 | g.49612452A>G | CA364398357 | RHAG | c.890T>C (p.Met297Thr) n.580T>C | |
6 | g.49612452A>T | CA364398353 | RHAG | c.890T>A (p.Met297Lys) n.580T>A | |
6 | g.49612453T>A | CA364398365 | RHAG | c.889A>T (p.Met297Leu) n.579A>T | |
6 | g.49612453T>C | CA364398376 | RHAG | c.889A>G (p.Met297Val) n.579A>G | |
6 | g.49612453T>G | CA364398366 | RHAG | c.889A>C (p.Met297Leu) n.579A>C | |
6 | g.49612454A>C | CA450401533 | RHAG | c.888T>G (p.Ser296=) n.578T>G | |
6 | g.49612454A>G | CA450401535 | RHAG | c.888T>C (p.Ser296=) n.578T>C | |
6 | g.49612454A>T | CA450401536 | RHAG | c.888T>A (p.Ser296=) n.578T>A | |
6 | g.49612455G>A | CA364398377 | RHAG | c.887C>T (p.Ser296Phe) n.577C>T | dbSNP |
6 | g.49612455G>C | CA364398384 | RHAG | c.887C>G (p.Ser296Cys) n.577C>G | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49612455G= | CA1627469048 | RHAG | c.887C= (p.Ser296=) n.577C= | |
6 | g.49612455G>T | CA364398380 | RHAG | c.887C>A (p.Ser296Tyr) n.577C>A | |
6 | g.49612456A>C | CA364398387 | RHAG | c.886T>G (p.Ser296Ala) n.576T>G | |
6 | g.49612456A>G | CA364398393 | RHAG | c.886T>C (p.Ser296Pro) n.576T>C | |
6 | g.49612456A>T | CA364398391 | RHAG | c.886T>A (p.Ser296Thr) n.576T>A | |
6 | g.49612457A>C | CA450401538 | RHAG | c.885T>G (p.Gly295=) n.575T>G | |
6 | g.49612457A>G | CA450401539 | RHAG | c.885T>C (p.Gly295=) n.575T>C | |
6 | g.49612457A>T | CA450401540 | RHAG | c.885T>A (p.Gly295=) n.575T>A | |
6 | g.49612458C>A | CA3847795 | RHAG | c.884G>T (p.Gly295Val) n.574G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612458C= | CA1627469050 | RHAG | c.884G= (p.Gly295=) n.574G= | |
6 | g.49612458C>G | CA364398404 | RHAG | c.884G>C (p.Gly295Ala) n.574G>C | |
6 | g.49612458C>T | CA364398405 | RHAG | c.884G>A (p.Gly295Asp) n.574G>A | |
6 | g.49612459C>A | CA364398406 | RHAG | c.883G>T (p.Gly295Cys) n.573G>T | gnomAD v4 |
6 | g.49612459C>G | CA364398407 | RHAG | c.883G>C (p.Gly295Arg) n.573G>C | |
6 | g.49612459C>T | CA364398408 | RHAG | c.883G>A (p.Gly295Ser) n.573G>A | |
6 | g.49612460A>C | CA364398410 | RHAG | c.882T>G (p.Phe294Leu) n.572T>G | |
6 | g.49612460A>G | CA450401542 | RHAG | c.882T>C (p.Phe294=) n.572T>C | |
6 | g.49612460A>T | CA364398411 | RHAG | c.882T>A (p.Phe294Leu) n.572T>A | |
6 | g.49612461A= | CA1627469054 | RHAG | c.881T= (p.Phe294=) n.571T= | |
6 | g.49612461A>C | CA364398412 | RHAG | c.881T>G (p.Phe294Cys) n.571T>G | dbSNP |
6 | g.49612461A>G | CA364398413 | RHAG | c.881T>C (p.Phe294Ser) n.571T>C | |
6 | g.49612461A>T | CA364398414 | RHAG | c.881T>A (p.Phe294Tyr) n.571T>A | |
6 | g.49612462A= | CA1627469059 | RHAG | c.880T= (p.Phe294=) n.570T= | |
6 | g.49612462A>C | CA364398415 | RHAG | c.880T>G (p.Phe294Val) n.570T>G | |
6 | g.49612462A>G | CA3847796 | RHAG | c.880T>C (p.Phe294Leu) n.570T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612462A>T | CA364398417 | RHAG | c.880T>A (p.Phe294Ile) n.570T>A | |
6 | g.49612463T>A | CA450401544 | RHAG | c.879A>T (p.Pro293=) n.569A>T | |
6 | g.49612463T>C | CA3847797 | RHAG | c.879A>G (p.Pro293=) n.569A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612463T>G | CA450401543 | RHAG | c.879A>C (p.Pro293=) n.569A>C | |
6 | g.49612463T= | CA1627469064 | RHAG | c.879A= (p.Pro293=) n.569A= | |
6 | g.49612464G>A | CA138843646 | RHAG | c.878C>T (p.Pro293Leu) n.568C>T | dbSNP |
6 | g.49612464G>C | CA364398419 | RHAG | c.878C>G (p.Pro293Arg) n.568C>G | |
6 | g.49612464G= | CA1627469068 | RHAG | c.878C= (p.Pro293=) n.568C= | |
6 | g.49612464G>T | CA364398420 | RHAG | c.878C>A (p.Pro293Gln) n.568C>A | gnomAD v4 |
6 | g.49612465G>A | CA364398424 | RHAG | c.877C>T (p.Pro293Ser) n.567C>T | |
6 | g.49612465G>C | CA364398425 | RHAG | c.877C>G (p.Pro293Ala) n.567C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612465G= | CA1627469072 | RHAG | c.877C= (p.Pro293=) n.567C= | |
6 | g.49612465G>T | CA364398426 | RHAG | c.877C>A (p.Pro293Thr) n.567C>A | gnomAD v4 |
6 | g.49612466G>A | CA450401547 | RHAG | c.876C>T (p.His292=) n.566C>T | |
6 | g.49612466G>C | CA364398427 | RHAG | c.876C>G (p.His292Gln) n.566C>G | |
6 | g.49612466G>T | CA364398428 | RHAG | c.876C>A (p.His292Gln) n.566C>A | |
6 | g.49612467T>A | CA364398430 | RHAG | c.875A>T (p.His292Leu) n.565A>T | |
6 | g.49612467T>C | CA364398432 | RHAG | c.875A>G (p.His292Arg) n.565A>G | |
6 | g.49612467T>G | CA364398429 | RHAG | c.875A>C (p.His292Pro) n.565A>C | |
6 | g.49612468G>A | CA364398433 | RHAG | c.874C>T (p.His292Tyr) n.564C>T | COSMIC |
6 | g.49612468G>C | CA364398434 | RHAG | c.874C>G (p.His292Asp) n.564C>G | |
6 | g.49612468G>T | CA364398435 | RHAG | c.874C>A (p.His292Asn) n.564C>A | gnomAD v4 |
6 | g.49612469A= | CA1627469119 | RHAG | c.873T= (p.Ile291=) n.563T= | |
6 | g.49612469A>C | CA364398436 | RHAG | c.873T>G (p.Ile291Met) n.563T>G | |
6 | g.49612469A>G | CA450401551 | RHAG | c.873T>C (p.Ile291=) n.563T>C | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612469A>T | CA450401550 | RHAG | c.873T>A (p.Ile291=) n.563T>A | |
6 | g.49612470A= | CA1627469127 | RHAG | c.872T= (p.Ile291=) n.562T= | |
6 | g.49612470A>C | CA364398441 | RHAG | c.872T>G (p.Ile291Ser) n.562T>G | |
6 | g.49612470A>G | CA364398439 | RHAG | c.872T>C (p.Ile291Thr) n.562T>C | dbSNP gnomAD v4 |
6 | g.49612470A>T | CA364398437 | RHAG | c.872T>A (p.Ile291Asn) n.562T>A | |
6 | g.49612471T>A | CA364398443 | RHAG | c.871A>T (p.Ile291Phe) n.561A>T | |
6 | g.49612471T>C | CA364398444 | RHAG | c.871A>G (p.Ile291Val) n.561A>G | gnomAD v4 |
6 | g.49612471T>G | CA364398445 | RHAG | c.871A>C (p.Ile291Leu) n.561A>C | |
6 | g.49612472T>A | CA450401554 | RHAG | c.870A>T (p.Ala290=) n.560A>T | |
6 | g.49612472T>C | CA450401555 | RHAG | c.870A>G (p.Ala290=) n.560A>G | |
6 | g.49612472T>G | CA450401556 | RHAG | c.870A>C (p.Ala290=) n.560A>C | |
6 | g.49612473G>A | CA364398447 | RHAG | c.869C>T (p.Ala290Val) n.559C>T | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49612473G>C | CA364398448 | RHAG | c.869C>G (p.Ala290Gly) n.559C>G | |
6 | g.49612473G= | CA1627469132 | RHAG | c.869C= (p.Ala290=) n.559C= | |
6 | g.49612473G>T | CA364398449 | RHAG | c.869C>A (p.Ala290Glu) n.559C>A | |
6 | g.49612474C>A | CA364398450 | RHAG | c.868G>T (p.Ala290Ser) n.558G>T | COSMIC |
6 | g.49612474C>G | CA364398453 | RHAG | c.868G>C (p.Ala290Pro) n.558G>C | |
6 | g.49612474C>T | CA364398451 | RHAG | c.868G>A (p.Ala290Thr) n.558G>A | |
6 | g.49612475C>A | CA364398454 | RHAG | c.867G>T (p.Met289Ile) n.557G>T | |
6 | g.49612475C>G | CA364398459 | RHAG | c.867G>C (p.Met289Ile) n.557G>C | |
6 | g.49612475C>T | CA364398460 | RHAG | c.867G>A (p.Met289Ile) n.557G>A | |
6 | g.49612476A>C | CA364398462 | RHAG | c.866T>G (p.Met289Arg) n.556T>G | |
6 | g.49612476A>G | CA364398463 | RHAG | c.866T>C (p.Met289Thr) n.556T>C | gnomAD v4 |
6 | g.49612476A>T | CA364398465 | RHAG | c.866T>A (p.Met289Lys) n.556T>A | |
6 | g.49612477T>A | CA364398466 | RHAG | c.865A>T (p.Met289Leu) n.555A>T | |
6 | g.49612477T>C | CA364398469 | RHAG | c.865A>G (p.Met289Val) n.555A>G | |
6 | g.49612477T>G | CA364398471 | RHAG | c.865A>C (p.Met289Leu) n.555A>C | |
6 | g.49612478A>C | CA364398473 | RHAG | c.864T>G (p.Asp288Glu) n.554T>G | |
6 | g.49612478A>G | CA450401558 | RHAG | c.864T>C (p.Asp288=) n.554T>C | |
6 | g.49612478A>T | CA364398474 | RHAG | c.864T>A (p.Asp288Glu) n.554T>A | |
6 | g.49612479T>A | CA3847798 | RHAG | c.863A>T (p.Asp288Val) n.553A>T | dbSNP ExAC gnomAD v2 |
6 | g.49612479T>C | CA364398477 | RHAG | c.863A>G (p.Asp288Gly) n.553A>G | |
6 | g.49612479T>G | CA364398475 | RHAG | c.863A>C (p.Asp288Ala) n.553A>C | |
6 | g.49612479T= | CA1627469140 | RHAG | c.863A= (p.Asp288=) n.553A= | |
6 | g.49612480C>A | CA364398482 | RHAG | c.862G>T (p.Asp288Tyr) n.552G>T | |
6 | g.49612480C= | CA1627469144 | RHAG | c.862G= (p.Asp288=) n.552G= | |
6 | g.49612480C>G | CA364398479 | RHAG | c.862G>C (p.Asp288His) n.552G>C | |
6 | g.49612480C>T | CA364398480 | RHAG | c.862G>A (p.Asp288Asn) n.552G>A | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49612481C>A | CA450401560 | RHAG | c.861G>T (p.Ala287=) n.551G>T | |
6 | g.49612481C= | CA1627469149 | RHAG | c.861G= (p.Ala287=) n.551G= | |
6 | g.49612481C>G | CA450401561 | RHAG | c.861G>C (p.Ala287=) n.551G>C | |
6 | g.49612481C>T | CA3847799 | RHAG | c.861G>A (p.Ala287=) n.551G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612482G>A | CA3847800 | RHAG | c.860C>T (p.Ala287Val) n.550C>T | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
6 | g.49612482G>C | CA364398484 | RHAG | c.860C>G (p.Ala287Gly) n.550C>G | |
6 | g.49612482G= | CA1627469150 | RHAG | c.860C= (p.Ala287=) n.550C= | |
6 | g.49612482G>T | CA364398485 | RHAG | c.860C>A (p.Ala287Glu) n.550C>A | |
6 | g.49612483C>A | CA364398486 | RHAG | c.859G>T (p.Ala287Ser) n.549G>T | |
6 | g.49612483C>G | CA364398487 | RHAG | c.859G>C (p.Ala287Pro) n.549G>C | |
6 | g.49612483C>T | CA364398488 | RHAG | c.859G>A (p.Ala287Thr) n.549G>A | |
6 | g.49612484A>C | CA364398490 | RHAG | c.858T>G (p.Cys286Trp) n.548T>G | |
6 | g.49612484A>G | CA450401562 | RHAG | c.858T>C (p.Cys286=) n.548T>C | |
6 | g.49612484A>T | CA364398491 | RHAG | c.858T>A (p.Cys286Ter) n.548T>A | |
6 | g.49612485C>A | CA364398496 | RHAG | c.857G>T (p.Cys286Phe) n.547G>T | |
6 | g.49612485C>G | CA364398494 | RHAG | c.857G>C (p.Cys286Ser) n.547G>C | |
6 | g.49612485C>T | CA364398493 | RHAG | c.857G>A (p.Cys286Tyr) n.547G>A | |
6 | g.49612486A>C | CA364398498 | RHAG | c.856T>G (p.Cys286Gly) n.546T>G | |
6 | g.49612486A>G | CA364398500 | RHAG | c.856T>C (p.Cys286Arg) n.546T>C | |
6 | g.49612486A>T | CA364398503 | RHAG | c.856T>A (p.Cys286Ser) n.546T>A | |
6 | g.49612487A= | CA1627469155 | RHAG | c.855T= (p.Thr285=) n.545T= | |
6 | g.49612487A>C | CA450401564 | RHAG | c.855T>G (p.Thr285=) n.545T>G | |
6 | g.49612487A>G | CA450401565 | RHAG | c.855T>C (p.Thr285=) n.545T>C | dbSNP |
6 | g.49612487A>T | CA450401566 | RHAG | c.855T>A (p.Thr285=) n.545T>A | |
6 | g.49612488G>A | CA364398505 | RHAG | c.854C>T (p.Thr285Ile) n.544C>T | |
6 | g.49612488G>C | CA364398508 | RHAG | c.854C>G (p.Thr285Ser) n.544C>G | |
6 | g.49612488G= | CA1627469161 | RHAG | c.854C= (p.Thr285=) n.544C= | |
6 | g.49612488G>T | CA364398509 | RHAG | c.854C>A (p.Thr285Asn) n.544C>A | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612489T>A | CA364398512 | RHAG | c.853A>T (p.Thr285Ser) n.543A>T | |
6 | g.49612489T>C | CA364398513 | RHAG | c.853A>G (p.Thr285Ala) n.543A>G | |
6 | g.49612489T>G | CA364398515 | RHAG | c.853A>C (p.Thr285Pro) n.543A>C | |
6 | g.49612490G>A | CA450401569 | RHAG | c.852C>T (p.Gly284=) n.542C>T | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612490G>C | CA450401570 | RHAG | c.852C>G (p.Gly284=) n.542C>G | |
6 | g.49612490G= | CA1627469167 | RHAG | c.852C= (p.Gly284=) n.542C= | |
6 | g.49612490G>T | CA450401571 | RHAG | c.852C>A (p.Gly284=) n.542C>A | |
6 | g.49612491C>A | CA364398516 | RHAG | c.851G>T (p.Gly284Val) n.541G>T | |
6 | g.49612491C>G | CA364398517 | RHAG | c.851G>C (p.Gly284Ala) n.541G>C | |
6 | g.49612491C>T | CA364398518 | RHAG | c.851G>A (p.Gly284Asp) n.541G>A | gnomAD v4 |
6 | g.49612492C>A | CA364398520 | RHAG | c.850G>T (p.Gly284Cys) n.540G>T | |
6 | g.49612492C>G | CA364398521 | RHAG | c.850G>C (p.Gly284Arg) n.540G>C | |
6 | g.49612492C>T | CA364398519 | RHAG | c.850G>A (p.Gly284Ser) n.540G>A | |
6 | g.49612493C>A | CA450401574 | RHAG | c.849G>T (p.Val283=) n.539G>T | |
6 | g.49612493C>G | CA450401575 | RHAG | c.849G>C (p.Val283=) n.539G>C | |
6 | g.49612493C>T | CA450401576 | RHAG | c.849G>A (p.Val283=) n.539G>A | |
6 | g.49612494A>C | CA364398522 | RHAG | c.848T>G (p.Val283Gly) n.538T>G | |
6 | g.49612494A>G | CA364398523 | RHAG | c.848T>C (p.Val283Ala) n.538T>C | |
6 | g.49612494A>T | CA364398524 | RHAG | c.848T>A (p.Val283Glu) n.538T>A | |
6 | g.49612495C>A | CA364398525 | RHAG | c.847G>T (p.Val283Leu) n.537G>T | |
6 | g.49612495C= | CA1627469172 | RHAG | c.847G= (p.Val283=) n.537G= | |
6 | g.49612495C>G | CA3847801 | RHAG | c.847G>C (p.Val283Leu) n.537G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49612495C>T | CA364398526 | RHAG | c.847G>A (p.Val283Met) n.537G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612496A>C | CA450401577 | RHAG | c.846T>G (p.Ala282=) n.536T>G | |
6 | g.49612496A>G | CA450401578 | RHAG | c.846T>C (p.Ala282=) n.536T>C | gnomAD v4 |
6 | g.49612496A>T | CA450401579 | RHAG | c.846T>A (p.Ala282=) n.536T>A | |
6 | g.49612497G>A | CA364398527 | RHAG | c.845C>T (p.Ala282Val) n.535C>T | |
6 | g.49612497G>C | CA364398528 | RHAG | c.845C>G (p.Ala282Gly) n.535C>G | gnomAD v4 |
6 | g.49612497G>T | CA364398529 | RHAG | c.845C>A (p.Ala282Asp) n.535C>A | |
6 | g.49612498C>A | CA364398530 | RHAG | c.844G>T (p.Ala282Ser) n.534G>T | |
6 | g.49612498C>G | CA364398531 | RHAG | c.844G>C (p.Ala282Pro) n.534G>C | |
6 | g.49612498C>T | CA364398532 | RHAG | c.844G>A (p.Ala282Thr) n.534G>A | gnomAD v4 |
6 | g.49612499A>C | CA450401581 | RHAG | c.843T>G (p.Val281=) n.533T>G | |
6 | g.49612499A>G | CA450401582 | RHAG | c.843T>C (p.Val281=) n.533T>C | |
6 | g.49612499A>T | CA450401583 | RHAG | c.843T>A (p.Val281=) n.533T>A | |
6 | g.49612500A= | CA1627469175 | RHAG | c.842T= (p.Val281=) n.532T= | |
6 | g.49612500A>C | CA364398534 | RHAG | c.842T>G (p.Val281Gly) n.532T>G | |
6 | g.49612500A>G | CA364398535 | RHAG | c.842T>C (p.Val281Ala) n.532T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49612500A>T | CA364398533 | RHAG | c.842T>A (p.Val281Asp) n.532T>A | |
6 | g.49612501C>A | CA364398536 | RHAG | c.841G>T (p.Val281Phe) n.531G>T | |
6 | g.49612501C>G | CA364398537 | RHAG | c.841G>C (p.Val281Leu) n.531G>C | |
6 | g.49612501C>T | CA364398538 | RHAG | c.841G>A (p.Val281Ile) n.531G>A | |
6 | g.49612502T>A | CA450401585 | RHAG | c.840A>T (p.Gly280=) n.530A>T | |
6 | g.49612502T>C | CA450401586 | RHAG | c.840A>G (p.Gly280=) n.530A>G | |
6 | g.49612502T>G | CA450401587 | RHAG | c.840A>C (p.Gly280=) n.530A>C | |
6 | g.49612503C>A | CA364398539 | RHAG | c.839G>T (p.Gly280Val) n.529G>T | |
6 | g.49612503C>G | CA364398540 | RHAG | c.839G>C (p.Gly280Ala) n.529G>C | gnomAD v4 |
6 | g.49612503C>T | CA364398541 | RHAG | c.839G>A (p.Gly280Glu) n.529G>A | |
6 | g.49612504C>A | CA364398543 | RHAG | c.838G>T (p.Gly280Ter) n.528G>T | |
6 | g.49612504C= | CA1627469181 | RHAG | c.838G= (p.Gly280=) n.528G= | |
6 | g.49612504C>G | CA364398542 | RHAG | c.838G>C (p.Gly280Arg) n.528G>C | |
6 | g.49612504C>T | CA357864 | RHAG | c.838G>A (p.Gly280Arg) n.528G>A | dbSNP gnomAD v4 |
6 | g.[49612504C>T;49612534C>T] | CA357865 | RHAG | c.[808G>A;838G>A] (p.[Val270Ile;Gly280Arg]) n.[498G>A;528G>A] | |
6 | g.49612505T>A | CA450401591 | RHAG | c.837A>T (p.Gly279=) n.527A>T | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612505T>C | CA450401592 | RHAG | c.837A>G (p.Gly279=) n.527A>G | gnomAD v4 |
6 | g.49612505T>G | CA450401593 | RHAG | c.837A>C (p.Gly279=) n.527A>C | |
6 | g.49612505T= | CA1627469187 | RHAG | c.837A= (p.Gly279=) n.527A= | |
6 | g.49612506C>A | CA364398544 | RHAG | c.836G>T (p.Gly279Val) n.526G>T | |
6 | g.49612506C= | CA1627469194 | RHAG | c.836G= (p.Gly279=) n.526G= | |
6 | g.49612506C>G | CA364398545 | RHAG | c.836G>C (p.Gly279Ala) n.526G>C | dbSNP |
6 | g.49612506C>T | CA122828 | RHAG | c.836G>A (p.Gly279Glu) n.526G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49612507C>A | CA364398546 | RHAG | c.835G>T (p.Gly279Ter) n.525G>T | COSMIC |
6 | g.49612507C>G | CA364398547 | RHAG | c.835G>C (p.Gly279Arg) n.525G>C | |
6 | g.49612507C>T | CA364398548 | RHAG | c.835G>A (p.Gly279Arg) n.525G>A | |
6 | g.49612508A= | CA1627469198 | RHAG | c.834T= (p.Ala278=) n.524T= | |
6 | g.49612508A>C | CA3847802 | RHAG | c.834T>G (p.Ala278=) n.524T>G | dbSNP ExAC gnomAD v2 |
6 | g.49612508A>G | CA450401595 | RHAG | c.834T>C (p.Ala278=) n.524T>C | gnomAD v4 |
6 | g.49612508A>T | CA450401596 | RHAG | c.834T>A (p.Ala278=) n.524T>A | |
6 | g.49612509G>A | CA364398550 | RHAG | c.833C>T (p.Ala278Val) n.523C>T | |
6 | g.49612509G>C | CA364398549 | RHAG | c.833C>G (p.Ala278Gly) n.523C>G | |
6 | g.49612509G>T | CA364398551 | RHAG | c.833C>A (p.Ala278Asp) n.523C>A |