| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.49636592del | CA2576917179 | RRAS | c.453+30del (n.453+30del) n.593+30del | |
| 19 | g.49636592G>A | CA2586409081 | RRAS | c.453+27C>T (n.453+27C>T) n.593+27C>T | gnomAD v4 |
| 19 | g.49636592G= | CA2340507961 | RRAS | c.453+27C= (n.453+27C=) n.593+27C= | |
| 19 | g.49636592G>T | CA9579014 | RRAS | c.453+27C>A (n.453+27C>A) n.593+27C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636593T= | CA2340507962 | RRAS | c.453+26A= (n.453+26A=) n.593+26A= | |
| 19 | g.49636594C>A | CA2560270867 | RRAS | c.453+25G>T (n.453+25G>T) n.593+25G>T | gnomAD v4 |
| 19 | g.49636594C= | CA2340507963 | RRAS | c.453+25G= (n.453+25G=) n.593+25G= | |
| 19 | g.49636594C>T | CA633644819 | RRAS | c.453+25G>A (n.453+25G>A) n.593+25G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636597dup | CA633644818 | RRAS | c.453+25dup (n.453+25dup) n.593+25dup | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.49636597del | CA2576917182 | RRAS | c.453+25del (n.453+25del) n.593+25del | gnomAD v4 |
| 19 | g.49636597C= | CA2340507964 | RRAS | c.453+22G= (n.453+22G=) n.593+22G= | |
| 19 | g.49636597C>G | CA2586409082 | RRAS | c.453+22G>C (n.453+22G>C) n.593+22G>C | gnomAD v4 |
| 19 | g.49636597C>T | CA309505599 | RRAS | c.453+22G>A (n.453+22G>A) n.593+22G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636598A>G | CA2586409083 | RRAS | c.453+21T>C (n.453+21T>C) n.593+21T>C | gnomAD v4 |
| 19 | g.49636599G>A | CA9579015 | RRAS | c.453+20C>T (n.453+20C>T) n.593+20C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636599G= | CA2340507965 | RRAS | c.453+20C= (n.453+20C=) n.593+20C= | |
| 19 | g.49636599G>T | CA2586409084 | RRAS | c.453+20C>A (n.453+20C>A) n.593+20C>A | gnomAD v4 |
| 19 | g.49636601A>G | CA2573156592 | RRAS | c.453+18T>C (n.453+18T>C) n.593+18T>C | ClinVar dbSNP gnomAD v4 |
| 19 | g.49636602A>G | CA2580097564 | RRAS | c.453+17T>C (n.453+17T>C) n.593+17T>C | ClinVar |
| 19 | g.49636603G>A | CA2340507967 | RRAS | c.453+16C>T (n.453+16C>T) n.593+16C>T | dbSNP gnomAD v4 |
| 19 | g.49636603G>C | CA2576917183 | RRAS | c.453+16C>G (n.453+16C>G) n.593+16C>G | |
| 19 | g.49636603G= | CA2340507966 | RRAS | c.453+16C= (n.453+16C=) n.593+16C= | |
| 19 | g.49636603G>T | CA2586409085 | RRAS | c.453+16C>A (n.453+16C>A) n.593+16C>A | gnomAD v4 |
| 19 | g.49636605G>C | CA9579016 | RRAS | c.453+14C>G (n.453+14C>G) n.593+14C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636605G= | CA2340507968 | RRAS | c.453+14C= (n.453+14C=) n.593+14C= | |
| 19 | g.49636605G>T | CA2586409087 | RRAS | c.453+14C>A (n.453+14C>A) n.593+14C>A | gnomAD v4 |
| 19 | g.49636608dup | CA2586409086 | RRAS | c.453+14dup (n.453+14dup) n.593+14dup | gnomAD v4 |
| 19 | g.49636608del | CA2576917184 | RRAS | c.453+14del (n.453+14del) n.593+14del | |
| 19 | g.49636606G>A | CA2548317608 | RRAS | c.453+13C>T (n.453+13C>T) n.593+13C>T | |
| 19 | g.49636606G>T | CA2576917185 | RRAS | c.453+13C>A (n.453+13C>A) n.593+13C>A | |
| 19 | g.49636607G= | CA2340507969 | RRAS | c.453+12C= (n.453+12C=) n.593+12C= | |
| 19 | g.49636607G>T | CA633644824 | RRAS | c.453+12C>A (n.453+12C>A) n.593+12C>A | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.49636608G= | CA2340507970 | RRAS | c.453+11C= (n.453+11C=) n.593+11C= | |
| 19 | g.49636608G>T | CA9579017 | RRAS | c.453+11C>A (n.453+11C>A) n.593+11C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.49636610_49636611del | CA2814696113 | RRAS | c.453+10_453+11del (n.453+10_453+11del) n.593+10_593+11del | |
| 19 | g.49636609T>A | CA996721595 | RRAS | c.453+10A>T (n.453+10A>T) n.593+10A>T | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.49636609T= | CA2340507971 | RRAS | c.453+10A= (n.453+10A=) n.593+10A= | |
| 19 | g.49636610del | CA2576917186 | RRAS | c.453+9del (n.453+9del) n.593+9del | |
| 19 | g.49636610G>A | CA633644827 | RRAS | c.453+9C>T (n.453+9C>T) n.593+9C>T | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.49636610G= | CA2340507972 | RRAS | c.453+9C= (n.453+9C=) n.593+9C= | |
| 19 | g.49636610G>T | CA2586409088 | RRAS | c.453+9C>A (n.453+9C>A) n.593+9C>A | gnomAD v4 |
| 19 | g.49636611T>C | CA2586409089 | RRAS | c.453+8A>G (n.453+8A>G) n.593+8A>G | gnomAD v4 |
| 19 | g.49636611T>G | CA2814696114 | RRAS | c.453+8A>C (n.453+8A>C) n.593+8A>C | |
| 19 | g.49636612C>A | CA2576917187 | RRAS | c.453+7G>T (n.453+7G>T) n.593+7G>T | |
| 19 | g.49636612C>T | CA2499225545 | RRAS | c.453+7G>A (n.453+7G>A) n.593+7G>A | ClinVar dbSNP |
| 19 | g.49636613C= | CA2340507973 | RRAS | c.453+6G= (n.453+6G=) n.593+6G= | |
| 19 | g.49636613C>T | CA9579018 | RRAS | c.453+6G>A (n.453+6G>A) n.593+6G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636614C= | CA2340507974 | RRAS | c.453+5G= (n.453+5G=) n.593+5G= | |
| 19 | g.49636614C>G | CA2586409090 | RRAS | c.453+5G>C (n.453+5G>C) n.593+5G>C | gnomAD v4 |
| 19 | g.49636614C>T | CA9579019 | RRAS | c.453+5G>A (n.453+5G>A) n.593+5G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636615G>A | CA9579020 | RRAS | c.453+4C>T (n.453+4C>T) n.593+4C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636615G= | CA2340507975 | RRAS | c.453+4C= (n.453+4C=) n.593+4C= | |
| 19 | g.49636617A= | CA2340507976 | RRAS | c.453+2T= (n.453+2T=) n.593+2T= | |
| 19 | g.49636617A>C | CA406845962 | RRAS | c.453+2T>G (n.453+2T>G) n.593+2T>G | |
| 19 | g.49636617A>G | CA9579021 | RRAS | c.453+2T>C (n.453+2T>C) n.593+2T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.49636617A>T | CA406845961 | RRAS | c.453+2T>A (n.453+2T>A) n.593+2T>A | |
| 19 | g.49636618C>A | CA406845963 | RRAS | c.453+1G>T (n.453+1G>T) n.593+1G>T | |
| 19 | g.49636618C>G | CA406845964 | RRAS | c.453+1G>C (n.453+1G>C) n.593+1G>C | |
| 19 | g.49636618C>T | CA406845965 | RRAS | c.453+1G>A (n.453+1G>A) n.593+1G>A | |
| 19 | g.49636619C>A | CA406845966 | RRAS | c.453G>T (p.Gln151His) n.593G>T | |
| 19 | g.49636619C= | CA2340507977 | RRAS | c.453G= (p.Gln151=) n.593G= | |
| 19 | g.49636619C>G | CA406845967 | RRAS | c.453G>C (p.Gln151His) n.593G>C | |
| 19 | g.49636619C>T | CA508130430 | RRAS | c.453G>A (p.Gln151=) n.593G>A | dbSNP |
| 19 | g.49636620T>A | CA406845968 | RRAS | c.452A>T (p.Gln151Leu) n.592A>T | |
| 19 | g.49636620T>C | CA406845969 | RRAS | c.452A>G (p.Gln151Arg) n.592A>G | |
| 19 | g.49636620T>G | CA406845970 | RRAS | c.452A>C (p.Gln151Pro) n.592A>C | gnomAD v4 |
| 19 | g.49636621G>A | CA406845971 | RRAS | c.451C>T (p.Gln151Ter) n.591C>T | |
| 19 | g.49636621G>C | CA406845972 | RRAS | c.451C>G (p.Gln151Glu) n.591C>G | |
| 19 | g.49636621G>T | CA406845973 | RRAS | c.451C>A (p.Gln151Lys) n.591C>A | |
| 19 | g.49636622G>A | CA508130434 | RRAS | c.450C>T (p.Arg150=) n.590C>T | |
| 19 | g.49636622G>C | CA508130435 | RRAS | c.450C>G (p.Arg150=) n.590C>G | |
| 19 | g.49636622G>T | CA508130436 | RRAS | c.450C>A (p.Arg150=) n.590C>A | |
| 19 | g.49636623C>A | CA406845974 | RRAS | c.449G>T (p.Arg150Leu) n.589G>T | |
| 19 | g.49636623C= | CA2340507978 | RRAS | c.449G= (p.Arg150=) n.589G= | |
| 19 | g.49636623C>G | CA406845975 | RRAS | c.449G>C (p.Arg150Pro) n.589G>C | ClinVar dbSNP |
| 19 | g.49636623C>T | CA309505659 | RRAS | c.449G>A (p.Arg150His) n.589G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636624G>A | CA9579022 | RRAS | c.448C>T (p.Arg150Cys) n.588C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636624G>C | CA406845976 | RRAS | c.448C>G (p.Arg150Gly) n.588C>G | |
| 19 | g.49636624G= | CA2340507979 | RRAS | c.448C= (p.Arg150=) n.588C= | |
| 19 | g.49636624G>T | CA406845977 | RRAS | c.448C>A (p.Arg150Ser) n.588C>A | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.49636625del | CA2586409091 | RRAS | c.447del (p.Gln149HisfsTer?) n.587del | gnomAD v4 |
| 19 | g.49636625C>A | CA406845978 | RRAS | c.447G>T (p.Gln149His) n.587G>T | |
| 19 | g.49636625C>G | CA406845979 | RRAS | c.447G>C (p.Gln149His) n.587G>C | |
| 19 | g.49636625C>T | CA508130438 | RRAS | c.447G>A (p.Gln149=) n.587G>A | |
| 19 | g.49636626T>A | CA406845980 | RRAS | c.446A>T (p.Gln149Leu) n.586A>T | |
| 19 | g.49636626T>C | CA309505661 | RRAS | c.446A>G (p.Gln149Arg) n.586A>G | dbSNP |
| 19 | g.49636626T>G | CA406845981 | RRAS | c.446A>C (p.Gln149Pro) n.586A>C | |
| 19 | g.49636626T= | CA2340507980 | RRAS | c.446A= (p.Gln149=) n.586A= | |
| 19 | g.49636627G>A | CA406845982 | RRAS | c.445C>T (p.Gln149Ter) n.585C>T | |
| 19 | g.49636627G>C | CA406845983 | RRAS | c.445C>G (p.Gln149Glu) n.585C>G | gnomAD v4 |
| 19 | g.49636627G= | CA2340507981 | RRAS | c.445C= (p.Gln149=) n.585C= | |
| 19 | g.49636627G>T | CA406845984 | RRAS | c.445C>A (p.Gln149Lys) n.585C>A | |
| 19 | g.49636628T>A | CA508130442 | RRAS | c.444A>T (p.Ser148=) n.584A>T | |
| 19 | g.49636628T>C | CA508130440 | RRAS | c.444A>G (p.Ser148=) n.584A>G | |
| 19 | g.49636628T>G | CA508130439 | RRAS | c.444A>C (p.Ser148=) n.584A>C | |
| 19 | g.49636628dup | CA2340507982 | RRAS | c.444dup (p.Gln149ThrfsTer22) n.584dup | dbSNP |
| 19 | g.49636629G>A | CA406845986 | RRAS | c.443C>T (p.Ser148Leu) n.583C>T | |
| 19 | g.49636629G>C | CA406845987 | RRAS | c.443C>G (p.Ser148Ter) n.583C>G | |
| 19 | g.49636629G>T | CA406845985 | RRAS | c.443C>A (p.Ser148Ter) n.583C>A | |
| 19 | g.49636630A>C | CA406845990 | RRAS | c.442T>G (p.Ser148Ala) n.582T>G | |
| 19 | g.49636630A>G | CA406845988 | RRAS | c.442T>C (p.Ser148Pro) n.582T>C | |
| 19 | g.49636630A>T | CA406845989 | RRAS | c.442T>A (p.Ser148Thr) n.582T>A | |
| 19 | g.49636631C>A | CA406845991 | RRAS | c.441G>T (p.Glu147Asp) n.581G>T | |
| 19 | g.49636631C= | CA2340507983 | RRAS | c.441G= (p.Glu147=) n.581G= | |
| 19 | g.49636631C>G | CA406845992 | RRAS | c.441G>C (p.Glu147Asp) n.581G>C | |
| 19 | g.49636631C>T | CA9579023 | RRAS | c.441G>A (p.Glu147=) n.581G>A | ClinVar dbSNP ExAC |
| 19 | g.49636632T>A | CA406845993 | RRAS | c.440A>T (p.Glu147Val) n.580A>T | dbSNP |
| 19 | g.49636632T>C | CA406845994 | RRAS | c.440A>G (p.Glu147Gly) n.580A>G | |
| 19 | g.49636632T>G | CA406845995 | RRAS | c.440A>C (p.Glu147Ala) n.580A>C | |
| 19 | g.49636632T= | CA2340507984 | RRAS | c.440A= (p.Glu147=) n.580A= | |
| 19 | g.49636633C>A | CA406845996 | RRAS | c.439G>T (p.Glu147Ter) n.579G>T | |
| 19 | g.49636633C>G | CA406845997 | RRAS | c.439G>C (p.Glu147Gln) n.579G>C | COSMIC |
| 19 | g.49636633C>T | CA406845998 | RRAS | c.439G>A (p.Glu147Lys) n.579G>A | gnomAD v4 |
| 19 | g.49636634C>A | CA508130445 | RRAS | c.438G>T (p.Leu146=) n.578G>T | ClinVar dbSNP COSMIC |
| 19 | g.49636634C= | CA2340507985 | RRAS | c.438G= (p.Leu146=) n.578G= | |
| 19 | g.49636634C>G | CA508130448 | RRAS | c.438G>C (p.Leu146=) n.578G>C | |
| 19 | g.49636634C>T | CA508130447 | RRAS | c.438G>A (p.Leu146=) n.578G>A | |
| 19 | g.49636635A= | CA2340507986 | RRAS | c.437T= (p.Leu146=) n.577T= | |
| 19 | g.49636635A>C | CA406846001 | RRAS | c.437T>G (p.Leu146Arg) n.577T>G | |
| 19 | g.49636635A>G | CA406846000 | RRAS | c.437T>C (p.Leu146Pro) n.577T>C | dbSNP gnomAD v4 |
| 19 | g.49636635A>T | CA406845999 | RRAS | c.437T>A (p.Leu146Gln) n.577T>A | |
| 19 | g.49636636G>A | CA508130449 | RRAS | c.436C>T (p.Leu146=) n.576C>T | |
| 19 | g.49636636G>C | CA406846002 | RRAS | c.436C>G (p.Leu146Val) n.576C>G | |
| 19 | g.49636636G>T | CA406846003 | RRAS | c.436C>A (p.Leu146Met) n.576C>A | ClinVar COSMIC |
| 19 | g.49636637A>C | CA406846004 | RRAS | c.435T>G (p.Asp145Glu) n.575T>G | |
| 19 | g.49636637A>G | CA508130453 | RRAS | c.435T>C (p.Asp145=) n.575T>C | |
| 19 | g.49636637A>T | CA406846005 | RRAS | c.435T>A (p.Asp145Glu) n.575T>A | |
| 19 | g.49636638T>A | CA406846006 | RRAS | c.434A>T (p.Asp145Val) n.574A>T | |
| 19 | g.49636638T>C | CA406846007 | RRAS | c.434A>G (p.Asp145Gly) n.574A>G | |
| 19 | g.49636638T>G | CA406846008 | RRAS | c.434A>C (p.Asp145Ala) n.574A>C | |
| 19 | g.49636639C>A | CA406846009 | RRAS | c.433G>T (p.Asp145Tyr) n.573G>T | |
| 19 | g.49636639C>G | CA406846010 | RRAS | c.433G>C (p.Asp145His) n.573G>C | |
| 19 | g.49636639C>T | CA406846011 | RRAS | c.433G>A (p.Asp145Asn) n.573G>A | |
| 19 | g.49636640T>A | CA508130456 | RRAS | c.432A>T (p.Ala144=) n.572A>T | |
| 19 | g.49636640T>C | CA508130457 | RRAS | c.432A>G (p.Ala144=) n.572A>G | |
| 19 | g.49636640T>G | CA508130458 | RRAS | c.432A>C (p.Ala144=) n.572A>C | |
| 19 | g.49636641G>A | CA406846012 | RRAS | c.431C>T (p.Ala144Val) n.571C>T | |
| 19 | g.49636641G>C | CA406846013 | RRAS | c.431C>G (p.Ala144Gly) n.571C>G | |
| 19 | g.49636641G>T | CA406846014 | RRAS | c.431C>A (p.Ala144Glu) n.571C>A | |
| 19 | g.49636642C>A | CA406846016 | RRAS | c.430G>T (p.Ala144Ser) n.570G>T | |
| 19 | g.49636642C>G | CA406846017 | RRAS | c.430G>C (p.Ala144Pro) n.570G>C | |
| 19 | g.49636642C>T | CA406846015 | RRAS | c.430G>A (p.Ala144Thr) n.570G>A | |
| 19 | g.49636643C>A | CA406846018 | RRAS | c.429G>T (p.Lys143Asn) n.569G>T | |
| 19 | g.49636643C>G | CA406846019 | RRAS | c.429G>C (p.Lys143Asn) n.569G>C | |
| 19 | g.49636643C>T | CA508130462 | RRAS | c.429G>A (p.Lys143=) n.569G>A | |
| 19 | g.49636644T>A | CA406846020 | RRAS | c.428A>T (p.Lys143Met) n.568A>T | |
| 19 | g.49636644T>C | CA406846021 | RRAS | c.428A>G (p.Lys143Arg) n.568A>G | dbSNP |
| 19 | g.49636644T>G | CA406846022 | RRAS | c.428A>C (p.Lys143Thr) n.568A>C | |
| 19 | g.49636644T= | CA2340507987 | RRAS | c.428A= (p.Lys143=) n.568A= | |
| 19 | g.49636645T>A | CA309505665 | RRAS | c.427A>T (p.Lys143Ter) n.567A>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636645T>C | CA406846023 | RRAS | c.427A>G (p.Lys143Glu) n.567A>G | |
| 19 | g.49636645T>G | CA406846024 | RRAS | c.427A>C (p.Lys143Gln) n.567A>C | |
| 19 | g.49636645T= | CA2340507988 | RRAS | c.427A= (p.Lys143=) n.567A= | |
| 19 | g.49636646G>A | CA508130466 | RRAS | c.426C>T (p.Asn142=) n.566C>T | |
| 19 | g.49636646G>C | CA406846025 | RRAS | c.426C>G (p.Asn142Lys) n.566C>G | |
| 19 | g.49636646G>T | CA406846026 | RRAS | c.426C>A (p.Asn142Lys) n.566C>A | gnomAD v4 |
| 19 | g.49636647T>A | CA406846027 | RRAS | c.425A>T (p.Asn142Ile) n.565A>T | |
| 19 | g.49636647T>C | CA406846028 | RRAS | c.425A>G (p.Asn142Ser) n.565A>G | gnomAD v4 |
| 19 | g.49636647T>G | CA406846029 | RRAS | c.425A>C (p.Asn142Thr) n.565A>C | |
| 19 | g.49636648T>A | CA406846032 | RRAS | c.424A>T (p.Asn142Tyr) n.564A>T | |
| 19 | g.49636648T>C | CA406846031 | RRAS | c.424A>G (p.Asn142Asp) n.564A>G | |
| 19 | g.49636648T>G | CA406846030 | RRAS | c.424A>C (p.Asn142His) n.564A>C | |
| 19 | g.49636648_49636649delinsTC | CA2340507989 | RRAS | c.423_424delinsGA (p.Gly141=) n.563_564delinsGA | |
| 19 | g.49636649C>A | CA508130474 | RRAS | c.423G>T (p.Gly141=) n.563G>T | COSMIC |
| 19 | g.49636649C>G | CA508130475 | RRAS | c.423G>C (p.Gly141=) n.563G>C | |
| 19 | g.49636649C>T | CA508130473 | RRAS | c.423G>A (p.Gly141=) n.563G>A | |
| 19 | g.49636651del | CA9579024 | RRAS | c.423del (p.Asn142ThrfsTer?) n.563del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636650C>A | CA406846033 | RRAS | c.422G>T (p.Gly141Val) n.562G>T | |
| 19 | g.49636650C= | CA2340507990 | RRAS | c.422G= (p.Gly141=) n.562G= | |
| 19 | g.49636650C>G | CA9579025 | RRAS | c.422G>C (p.Gly141Ala) n.562G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636650C>T | CA406846034 | RRAS | c.422G>A (p.Gly141Glu) n.562G>A | |
| 19 | g.49636651C>A | CA406846035 | RRAS | c.421G>T (p.Gly141Trp) n.561G>T | |
| 19 | g.49636651C= | CA2340507991 | RRAS | c.421G= (p.Gly141=) n.561G= | |
| 19 | g.49636651C>G | CA406846036 | RRAS | c.421G>C (p.Gly141Arg) n.561G>C | |
| 19 | g.49636651C>T | CA9579026 | RRAS | c.421G>A (p.Gly141Arg) n.561G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636652G>A | CA9579027 | RRAS | c.420C>T (p.Val140=) n.560C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636652G>C | CA508130483 | RRAS | c.420C>G (p.Val140=) n.560C>G | dbSNP gnomAD v2 |
| 19 | g.49636652G= | CA2340507992 | RRAS | c.420C= (p.Val140=) n.560C= | |
| 19 | g.49636652G>T | CA508130484 | RRAS | c.420C>A (p.Val140=) n.560C>A | gnomAD v4 |
| 19 | g.49636653A>C | CA406846037 | RRAS | c.419T>G (p.Val140Gly) n.559T>G | |
| 19 | g.49636653A>G | CA406846038 | RRAS | c.419T>C (p.Val140Ala) n.559T>C | |
| 19 | g.49636653A>T | CA406846039 | RRAS | c.419T>A (p.Val140Asp) n.559T>A | |
| 19 | g.49636654C>A | CA406846040 | RRAS | c.418G>T (p.Val140Phe) n.558G>T | COSMIC |
| 19 | g.49636654C= | CA2340507993 | RRAS | c.418G= (p.Val140=) n.558G= | |
| 19 | g.49636654C>G | CA406846041 | RRAS | c.418G>C (p.Val140Leu) n.558G>C | gnomAD v4 |
| 19 | g.49636654C>T | CA406846042 | RRAS | c.418G>A (p.Val140Ile) n.558G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636655C>A | CA406846043 | RRAS | c.417G>T (p.Leu139Phe) n.557G>T | |
| 19 | g.49636655C= | CA2340507994 | RRAS | c.417G= (p.Leu139=) n.557G= | |
| 19 | g.49636655C>G | CA406846044 | RRAS | c.417G>C (p.Leu139Phe) n.557G>C | dbSNP |
| 19 | g.49636655C>T | CA508130501 | RRAS | c.417G>A (p.Leu139=) n.557G>A | |
| 19 | g.49636659_49636663dup | CA2586409092 | RRAS | c.413_417dup (p.Val140CysfsTer?) n.553_557dup | gnomAD v4 |
| 19 | g.49636656A>C | CA406846045 | RRAS | c.416T>G (p.Leu139Trp) n.556T>G | |
| 19 | g.49636656A>G | CA406846047 | RRAS | c.416T>C (p.Leu139Ser) n.556T>C | |
| 19 | g.49636656A>T | CA406846046 | RRAS | c.416T>A (p.Leu139Ter) n.556T>A | |
| 19 | g.49636657A>C | CA406846226 | RRAS | c.415T>G (p.Leu139Val) n.555T>G | |
| 19 | g.49636657A>G | CA508290378 | RRAS | c.415T>C (p.Leu139=) n.555T>C | |
| 19 | g.49636657A>T | CA406846231 | RRAS | c.415T>A (p.Leu139Met) n.555T>A | |
| 19 | g.49636658C>A | CA508290381 | RRAS | c.414G>T (p.Val138=) n.554G>T | |
| 19 | g.49636658C= | CA2340507995 | RRAS | c.414G= (p.Val138=) n.554G= | |
| 19 | g.49636658C>G | CA508290385 | RRAS | c.414G>C (p.Val138=) n.554G>C | |
| 19 | g.49636658C>T | CA508290387 | RRAS | c.414G>A (p.Val138=) n.554G>A | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.49636659A>C | CA406846233 | RRAS | c.413T>G (p.Val138Gly) n.553T>G | |
| 19 | g.49636659A>G | CA406846236 | RRAS | c.413T>C (p.Val138Ala) n.553T>C | |
| 19 | g.49636659A>T | CA406846238 | RRAS | c.413T>A (p.Val138Glu) n.553T>A | |
| 19 | g.49636660C>A | CA406846243 | RRAS | c.412G>T (p.Val138Leu) n.552G>T | ClinVar dbSNP |
| 19 | g.49636660C>G | CA406846246 | RRAS | c.412G>C (p.Val138Leu) n.552G>C | ClinVar |
| 19 | g.49636660C>T | CA406846249 | RRAS | c.412G>A (p.Val138Met) n.552G>A | |
| 19 | g.49636661A>C | CA508290393 | RRAS | c.411T>G (p.Val137=) n.551T>G | |
| 19 | g.49636661A>G | CA508290394 | RRAS | c.411T>C (p.Val137=) n.551T>C | gnomAD v4 |
| 19 | g.49636661A>T | CA508290396 | RRAS | c.411T>A (p.Val137=) n.551T>A | |
| 19 | g.49636662A>C | CA406846254 | RRAS | c.410T>G (p.Val137Gly) n.550T>G | |
| 19 | g.49636662A>G | CA406846258 | RRAS | c.410T>C (p.Val137Ala) n.550T>C | |
| 19 | g.49636662A>T | CA406846262 | RRAS | c.410T>A (p.Val137Asp) n.550T>A | |
| 19 | g.49636663C>A | CA406846264 | RRAS | c.409G>T (p.Val137Phe) n.549G>T | |
| 19 | g.49636663C= | CA2340507996 | RRAS | c.409G= (p.Val137=) n.549G= | |
| 19 | g.49636663C>G | CA406846275 | RRAS | c.409G>C (p.Val137Leu) n.549G>C | |
| 19 | g.49636663C>T | CA9579028 | RRAS | c.409G>A (p.Val137Ile) n.549G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.49636664G>A | CA9579029 | RRAS | c.408C>T (p.Pro136=) n.548C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636664G>C | CA508290409 | RRAS | c.408C>G (p.Pro136=) n.548C>G | ClinVar dbSNP |
| 19 | g.49636664G= | CA2340507997 | RRAS | c.408C= (p.Pro136=) n.548C= | |
| 19 | g.49636664G>T | CA508290410 | RRAS | c.408C>A (p.Pro136=) n.548C>A | |
| 19 | g.49636665G>A | CA406846281 | RRAS | c.407C>T (p.Pro136Leu) n.547C>T | |
| 19 | g.49636665G>C | CA406846287 | RRAS | c.407C>G (p.Pro136Arg) n.547C>G | |
| 19 | g.49636665G>T | CA406846284 | RRAS | c.407C>A (p.Pro136His) n.547C>A | |
| 19 | g.49636666G>A | CA406846292 | RRAS | c.406C>T (p.Pro136Ser) n.546C>T | dbSNP |
| 19 | g.49636666G>C | CA406846297 | RRAS | c.406C>G (p.Pro136Ala) n.546C>G | gnomAD v4 |
| 19 | g.49636666G= | CA2340507998 | RRAS | c.406C= (p.Pro136=) n.546C= | |
| 19 | g.49636666G>T | CA406846299 | RRAS | c.406C>A (p.Pro136Thr) n.546C>A | |
| 19 | g.49636667G>A | CA508290420 | RRAS | c.405C>T (p.Phe135=) n.545C>T | gnomAD v4 COSMIC |
| 19 | g.49636667G>C | CA406846301 | RRAS | c.405C>G (p.Phe135Leu) n.545C>G | |
| 19 | g.49636667G>T | CA406846304 | RRAS | c.405C>A (p.Phe135Leu) n.545C>A | |
| 19 | g.49636668A>C | CA406846307 | RRAS | c.404T>G (p.Phe135Cys) n.544T>G | |
| 19 | g.49636668A>G | CA406846310 | RRAS | c.404T>C (p.Phe135Ser) n.544T>C | |
| 19 | g.49636668A>T | CA406846326 | RRAS | c.404T>A (p.Phe135Tyr) n.544T>A | |
| 19 | g.49636669A>C | CA406846331 | RRAS | c.403T>G (p.Phe135Val) n.543T>G | |
| 19 | g.49636669A>G | CA406846333 | RRAS | c.403T>C (p.Phe135Leu) n.543T>C | gnomAD v4 |
| 19 | g.49636669A>T | CA406846337 | RRAS | c.403T>A (p.Phe135Ile) n.543T>A | |
| 19 | g.49636670G>A | CA508290426 | RRAS | c.402C>T (p.Asp134=) n.542C>T | |
| 19 | g.49636670G>C | CA406846339 | RRAS | c.402C>G (p.Asp134Glu) n.542C>G | |
| 19 | g.49636670G>T | CA406846340 | RRAS | c.402C>A (p.Asp134Glu) n.542C>A | |
| 19 | g.49636671T>A | CA406846345 | RRAS | c.401A>T (p.Asp134Val) n.541A>T | |
| 19 | g.49636671T>C | CA406846347 | RRAS | c.401A>G (p.Asp134Gly) n.541A>G | |
| 19 | g.49636671T>G | CA406846350 | RRAS | c.401A>C (p.Asp134Ala) n.541A>C | |
| 19 | g.49636672C>A | CA406846351 | RRAS | c.400G>T (p.Asp134Tyr) n.540G>T | |
| 19 | g.49636672C= | CA2340507999 | RRAS | c.400G= (p.Asp134=) n.540G= | |
| 19 | g.49636672C>G | CA406846353 | RRAS | c.400G>C (p.Asp134His) n.540G>C | |
| 19 | g.49636672C>T | CA9579030 | RRAS | c.400G>A (p.Asp134Asn) n.540G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.49636673G>A | CA9579031 | RRAS | c.399C>T (p.Asp133=) n.539C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636673G>C | CA406846368 | RRAS | c.399C>G (p.Asp133Glu) n.539C>G | |
| 19 | g.49636673G= | CA2340508000 | RRAS | c.399C= (p.Asp133=) n.539C= | |
| 19 | g.49636673G>T | CA406846371 | RRAS | c.399C>A (p.Asp133Glu) n.539C>A | gnomAD v4 |
| 19 | g.49636674T>A | CA406846372 | RRAS | c.398A>T (p.Asp133Val) n.538A>T | |
| 19 | g.49636674T>C | CA406846373 | RRAS | c.398A>G (p.Asp133Gly) n.538A>G | |
| 19 | g.49636674T>G | CA406846374 | RRAS | c.398A>C (p.Asp133Ala) n.538A>C | |
| 19 | g.49636675C>A | CA406846379 | RRAS | c.397G>T (p.Asp133Tyr) n.537G>T | |
| 19 | g.49636675C= | CA2340508001 | RRAS | c.397G= (p.Asp133=) n.537G= | |
| 19 | g.49636675C>G | CA406846377 | RRAS | c.397G>C (p.Asp133His) n.537G>C | dbSNP gnomAD v4 |
| 19 | g.49636675C>T | CA9579032 | RRAS | c.397G>A (p.Asp133Asn) n.537G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636676G>A | CA9579033 | RRAS | c.396C>T (p.Arg132=) n.536C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.49636676G>C | CA508290441 | RRAS | c.396C>G (p.Arg132=) n.536C>G | |
| 19 | g.49636676G= | CA2340508002 | RRAS | c.396C= (p.Arg132=) n.536C= | |
| 19 | g.49636676G>T | CA508290443 | RRAS | c.396C>A (p.Arg132=) n.536C>A | |
| 19 | g.49636677C>A | CA406846389 | RRAS | c.395G>T (p.Arg132Leu) n.535G>T | gnomAD v4 |
| 19 | g.49636677C= | CA2340508003 | RRAS | c.395G= (p.Arg132=) n.535G= | |
| 19 | g.49636677C>G | CA406846392 | RRAS | c.395G>C (p.Arg132Pro) n.535G>C | |
| 19 | g.49636677C>T | CA9579034 | RRAS | c.395G>A (p.Arg132His) n.535G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636678G>A | CA9579035 | RRAS | c.394C>T (p.Arg132Cys) n.534C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636678G>C | CA406846398 | RRAS | c.394C>G (p.Arg132Gly) n.534C>G | |
| 19 | g.49636678G= | CA2340508004 | RRAS | c.394C= (p.Arg132=) n.534C= | |
| 19 | g.49636678G>T | CA406846399 | RRAS | c.394C>A (p.Arg132Ser) n.534C>A | |
| 19 | g.49636679G>A | CA508290454 | RRAS | c.393C>T (p.Asp131=) n.533C>T | |
| 19 | g.49636679G>C | CA406846410 | RRAS | c.393C>G (p.Asp131Glu) n.533C>G | |
| 19 | g.49636679G>T | CA406846414 | RRAS | c.393C>A (p.Asp131Glu) n.533C>A | |
| 19 | g.49636680T>A | CA406846418 | RRAS | c.392A>T (p.Asp131Val) n.532A>T | |
| 19 | g.49636680T>C | CA406846421 | RRAS | c.392A>G (p.Asp131Gly) n.532A>G | gnomAD v4 |
| 19 | g.49636680T>G | CA406846423 | RRAS | c.392A>C (p.Asp131Ala) n.532A>C | |
| 19 | g.49636681C>A | CA406846435 | RRAS | c.391G>T (p.Asp131Tyr) n.531G>T | |
| 19 | g.49636681C>G | CA406846430 | RRAS | c.391G>C (p.Asp131His) n.531G>C | |
| 19 | g.49636681C>T | CA406846426 | RRAS | c.391G>A (p.Asp131Asn) n.531G>A | |
| 19 | g.49636682C>A | CA406846437 | RRAS | c.390G>T (p.Lys130Asn) n.530G>T | |
| 19 | g.49636682C>G | CA406846440 | RRAS | c.390G>C (p.Lys130Asn) n.530G>C | |
| 19 | g.49636682C>T | CA508290462 | RRAS | c.390G>A (p.Lys130=) n.530G>A | |
| 19 | g.49636683T>A | CA406846446 | RRAS | c.389A>T (p.Lys130Met) n.529A>T | |
| 19 | g.49636683T>C | CA406846447 | RRAS | c.389A>G (p.Lys130Arg) n.529A>G | dbSNP gnomAD v4 |
| 19 | g.49636683T>G | CA406846451 | RRAS | c.389A>C (p.Lys130Thr) n.529A>C | |
| 19 | g.49636683T= | CA2340508005 | RRAS | c.389A= (p.Lys130=) n.529A= | |
| 19 | g.49636684T>A | CA406846453 | RRAS | c.388A>T (p.Lys130Ter) n.528A>T | |
| 19 | g.49636684T>C | CA406846455 | RRAS | c.388A>G (p.Lys130Glu) n.528A>G | |
| 19 | g.49636684T>G | CA406846456 | RRAS | c.388A>C (p.Lys130Gln) n.528A>C | |
| 19 | g.49636685G>A | CA508290470 | RRAS | c.387C>T (p.Val129=) n.527C>T | |
| 19 | g.49636685G>C | CA508290475 | RRAS | c.387C>G (p.Val129=) n.527C>G | |
| 19 | g.49636685G>T | CA508290476 | RRAS | c.387C>A (p.Val129=) n.527C>A | |
| 19 | g.49636686A>C | CA406846457 | RRAS | c.386T>G (p.Val129Gly) n.526T>G | |
| 19 | g.49636686A>G | CA406846458 | RRAS | c.386T>C (p.Val129Ala) n.526T>C | |
| 19 | g.49636686A>T | CA406846459 | RRAS | c.386T>A (p.Val129Asp) n.526T>A | |
| 19 | g.49636687C>A | CA406846462 | RRAS | c.385G>T (p.Val129Phe) n.525G>T | dbSNP |
| 19 | g.49636687C= | CA2340508006 | RRAS | c.385G= (p.Val129=) n.525G= | |
| 19 | g.49636687C>G | CA406846469 | RRAS | c.385G>C (p.Val129Leu) n.525G>C | |
| 19 | g.49636687C>T | CA309505724 | RRAS | c.385G>A (p.Val129Ile) n.525G>A | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.49636689del | CA2586409093 | RRAS | c.385del (p.Val129SerfsTer?) n.525del | gnomAD v4 |
| 19 | g.49636688C>A | CA508290488 | RRAS | c.384G>T (p.Arg128=) n.524G>T | |
| 19 | g.49636688C>G | CA508290489 | RRAS | c.384G>C (p.Arg128=) n.524G>C | gnomAD v4 |
| 19 | g.49636688C>T | CA508290490 | RRAS | c.384G>A (p.Arg128=) n.524G>A | gnomAD v4 |
| 19 | g.49636689C>A | CA406846478 | RRAS | c.383G>T (p.Arg128Leu) n.523G>T | |
| 19 | g.49636689C= | CA2340508007 | RRAS | c.383G= (p.Arg128=) n.523G= | |
| 19 | g.49636689C>G | CA406846476 | RRAS | c.383G>C (p.Arg128Pro) n.523G>C | |
| 19 | g.49636689C>T | CA9579036 | RRAS | c.383G>A (p.Arg128Gln) n.523G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.49636690G>A | CA406846480 | RRAS | c.382C>T (p.Arg128Trp) n.522C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 19 | g.49636690G>C | CA406846481 | RRAS | c.382C>G (p.Arg128Gly) n.522C>G | |
| 19 | g.49636690G= | CA2340508008 | RRAS | c.382C= (p.Arg128=) n.522C= | |
| 19 | g.49636690G>T | CA508290497 | RRAS | c.382C>A (p.Arg128=) n.522C>A | gnomAD v4 |
| 19 | g.49636691C>A | CA508290498 | RRAS | c.381G>T (p.Leu127=) n.521G>T | |
| 19 | g.49636691C>G | CA508290499 | RRAS | c.381G>C (p.Leu127=) n.521G>C | |
| 19 | g.49636691C>T | CA508290501 | RRAS | c.381G>A (p.Leu127=) n.521G>A | |
| 19 | g.49636692A>C | CA406846482 | RRAS | c.380T>G (p.Leu127Arg) n.520T>G | |
| 19 | g.49636692A>G | CA406846483 | RRAS | c.380T>C (p.Leu127Pro) n.520T>C | |
| 19 | g.49636692A>T | CA406846484 | RRAS | c.380T>A (p.Leu127Gln) n.520T>A |