| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.7184488A>C | CA403670022 | INSR | c.802T>G (p.Cys268Gly) n.777T>G c.880T>G (p.Cys294Gly) | |
| 19 | g.7184488A>G | CA403670023 | INSR | c.802T>C (p.Cys268Arg) n.777T>C c.880T>C (p.Cys294Arg) | |
| 19 | g.7184488A>T | CA403670024 | INSR | c.802T>A (p.Cys268Ser) n.777T>A c.880T>A (p.Cys294Ser) | |
| 19 | g.7184489G>A | CA505400467 | INSR | c.801C>T (p.Thr267=) n.776C>T c.879C>T (p.Thr293=) | |
| 19 | g.7184489G>C | CA505400469 | INSR | c.801C>G (p.Thr267=) n.776C>G c.879C>G (p.Thr293=) | gnomAD v4 |
| 19 | g.7184489G>T | CA505400468 | INSR | c.801C>A (p.Thr267=) n.776C>A c.879C>A (p.Thr293=) | |
| 19 | g.7184490G>A | CA403670025 | INSR | c.800C>T (p.Thr267Ile) n.775C>T c.878C>T (p.Thr293Ile) | |
| 19 | g.7184490G>C | CA403670026 | INSR | c.800C>G (p.Thr267Ser) n.775C>G c.878C>G (p.Thr293Ser) | |
| 19 | g.7184490G>T | CA403670027 | INSR | c.800C>A (p.Thr267Asn) n.775C>A c.878C>A (p.Thr293Asn) | |
| 19 | g.7184491T>A | CA403670028 | INSR | c.799A>T (p.Thr267Ser) n.774A>T c.877A>T (p.Thr293Ser) | |
| 19 | g.7184491T>C | CA403670030 | INSR | c.799A>G (p.Thr267Ala) n.774A>G c.877A>G (p.Thr293Ala) | |
| 19 | g.7184491T>G | CA403670029 | INSR | c.799A>C (p.Thr267Pro) n.774A>C c.877A>C (p.Thr293Pro) | |
| 19 | g.7184492C>A | CA403670031 | INSR | c.798G>T (p.Glu266Asp) n.773G>T c.876G>T (p.Glu292Asp) | |
| 19 | g.7184492C>G | CA403670032 | INSR | c.798G>C (p.Glu266Asp) n.773G>C c.876G>C (p.Glu292Asp) | |
| 19 | g.7184492C>T | CA505400470 | INSR | c.798G>A (p.Glu266=) n.773G>A c.876G>A (p.Glu292=) | |
| 19 | g.7184493T>A | CA403670035 | INSR | c.797A>T (p.Glu266Val) n.772A>T c.875A>T (p.Glu292Val) | |
| 19 | g.7184493T>C | CA403670037 | INSR | c.797A>G (p.Glu266Gly) n.772A>G c.875A>G (p.Glu292Gly) | |
| 19 | g.7184493T>G | CA403670039 | INSR | c.797A>C (p.Glu266Ala) n.772A>C c.875A>C (p.Glu292Ala) | |
| 19 | g.7184494C>A | CA403670041 | INSR | c.796G>T (p.Glu266Ter) n.771G>T c.874G>T (p.Glu292Ter) | |
| 19 | g.7184494C= | CA2320796266 | INSR | c.796G= (p.Glu266=) n.771G= c.874G= (p.Glu292=) | |
| 19 | g.7184494C>G | CA403670044 | INSR | c.796G>C (p.Glu266Gln) n.771G>C c.874G>C (p.Glu292Gln) | |
| 19 | g.7184494C>T | CA9136007 | INSR | c.796G>A (p.Glu266Lys) n.771G>A c.874G>A (p.Glu292Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184495C>A | CA505400471 | INSR | c.795G>T (p.Val265=) n.770G>T c.873G>T (p.Val291=) | |
| 19 | g.7184495C= | CA2320796268 | INSR | c.795G= (p.Val265=) n.770G= c.873G= (p.Val291=) | |
| 19 | g.7184495C>G | CA505400472 | INSR | c.795G>C (p.Val265=) n.770G>C c.873G>C (p.Val291=) | |
| 19 | g.7184495C>T | CA505400473 | INSR | c.795G>A (p.Val265=) n.770G>A c.873G>A (p.Val291=) | dbSNP gnomAD v4 |
| 19 | g.7184496A>C | CA403670047 | INSR | c.794T>G (p.Val265Gly) n.769T>G c.872T>G (p.Val291Gly) | |
| 19 | g.7184496A>G | CA403670050 | INSR | c.794T>C (p.Val265Ala) n.769T>C c.872T>C (p.Val291Ala) | |
| 19 | g.7184496A>T | CA403670052 | INSR | c.794T>A (p.Val265Glu) n.769T>A c.872T>A (p.Val291Glu) | |
| 19 | g.7184497C>A | CA403670055 | INSR | c.793G>T (p.Val265Leu) n.768G>T c.871G>T (p.Val291Leu) | |
| 19 | g.7184497C= | CA2320796270 | INSR | c.793G= (p.Val265=) n.768G= c.871G= (p.Val291=) | |
| 19 | g.7184497C>G | CA403670058 | INSR | c.793G>C (p.Val265Leu) n.768G>C c.871G>C (p.Val291Leu) | dbSNP |
| 19 | g.7184497C>T | CA9136008 | INSR | c.793G>A (p.Val265Met) n.768G>A c.871G>A (p.Val291Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184498A= | CA2320796273 | INSR | c.792T= (p.Cys264=) n.767T= c.870T= (p.Cys290=) | |
| 19 | g.7184498A>C | CA403670061 | INSR | c.792T>G (p.Cys264Trp) n.767T>G c.870T>G (p.Cys290Trp) | |
| 19 | g.7184498A>G | CA9136009 | INSR | c.792T>C (p.Cys264=) n.767T>C c.870T>C (p.Cys290=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184498A>T | CA403670064 | INSR | c.792T>A (p.Cys264Ter) n.767T>A c.870T>A (p.Cys290Ter) | |
| 19 | g.7184499C>A | CA403670068 | INSR | c.791G>T (p.Cys264Phe) n.766G>T c.869G>T (p.Cys290Phe) | |
| 19 | g.7184499C>G | CA403670070 | INSR | c.791G>C (p.Cys264Ser) n.766G>C c.869G>C (p.Cys290Ser) | |
| 19 | g.7184499C>T | CA403670073 | INSR | c.791G>A (p.Cys264Tyr) n.766G>A c.869G>A (p.Cys290Tyr) | |
| 19 | g.7184500A>C | CA403670076 | INSR | c.790T>G (p.Cys264Gly) n.765T>G c.868T>G (p.Cys290Gly) | |
| 19 | g.7184500A>G | CA403670078 | INSR | c.790T>C (p.Cys264Arg) n.765T>C c.868T>C (p.Cys290Arg) | |
| 19 | g.7184500A>T | CA403670080 | INSR | c.790T>A (p.Cys264Ser) n.765T>A c.868T>A (p.Cys290Ser) | |
| 19 | g.7184501C>A | CA403670083 | INSR | c.789G>T (p.Arg263Ser) n.764G>T c.867G>T (p.Arg289Ser) | |
| 19 | g.7184501C= | CA2320796276 | INSR | c.789G= (p.Arg263=) n.764G= c.867G= (p.Arg289=) | |
| 19 | g.7184501C>G | CA403670085 | INSR | c.789G>C (p.Arg263Ser) n.764G>C c.867G>C (p.Arg289Ser) | |
| 19 | g.7184501C>T | CA505400474 | INSR | c.789G>A (p.Arg263=) n.764G>A c.867G>A (p.Arg289=) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184502C>A | CA403670088 | INSR | c.788G>T (p.Arg263Met) n.763G>T c.866G>T (p.Arg289Met) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184502C= | CA2320796280 | INSR | c.788G= (p.Arg263=) n.763G= c.866G= (p.Arg289=) | |
| 19 | g.7184502C>G | CA9136010 | INSR | c.788G>C (p.Arg263Thr) n.763G>C c.866G>C (p.Arg289Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184502C>T | CA403670086 | INSR | c.788G>A (p.Arg263Lys) n.763G>A c.866G>A (p.Arg289Lys) | |
| 19 | g.7184503T>A | CA403670090 | INSR | c.787A>T (p.Arg263Trp) n.762A>T c.865A>T (p.Arg289Trp) | |
| 19 | g.7184503T>C | CA403670092 | INSR | c.787A>G (p.Arg263Gly) n.762A>G c.865A>G (p.Arg289Gly) | |
| 19 | g.7184503T>G | CA505400475 | INSR | c.787A>C (p.Arg263=) n.762A>C c.865A>C (p.Arg289=) | |
| 19 | g.7184504G>A | CA505400476 | INSR | c.786C>T (p.Gly262=) n.761C>T c.864C>T (p.Gly288=) | |
| 19 | g.7184504G>C | CA505400477 | INSR | c.786C>G (p.Gly262=) n.761C>G c.864C>G (p.Gly288=) | |
| 19 | g.7184504G>T | CA505400478 | INSR | c.786C>A (p.Gly262=) n.761C>A c.864C>A (p.Gly288=) | |
| 19 | g.7184505C>A | CA403670095 | INSR | c.785G>T (p.Gly262Val) n.760G>T c.863G>T (p.Gly288Val) | |
| 19 | g.7184505C= | CA2320796283 | INSR | c.785G= (p.Gly262=) n.760G= c.863G= (p.Gly288=) | |
| 19 | g.7184505C>G | CA403670097 | INSR | c.785G>C (p.Gly262Ala) n.760G>C c.863G>C (p.Gly288Ala) | |
| 19 | g.7184505C>T | CA9136011 | INSR | c.785G>A (p.Gly262Asp) n.760G>A c.863G>A (p.Gly288Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184506C>A | CA403670101 | INSR | c.784G>T (p.Gly262Cys) n.759G>T c.862G>T (p.Gly288Cys) | |
| 19 | g.7184506C= | CA2320796286 | INSR | c.784G= (p.Gly262=) n.759G= c.862G= (p.Gly288=) | |
| 19 | g.7184506C>G | CA403670104 | INSR | c.784G>C (p.Gly262Arg) n.759G>C c.862G>C (p.Gly288Arg) | |
| 19 | g.7184506C>T | CA9136012 | INSR | c.784G>A (p.Gly262Ser) n.759G>A c.862G>A (p.Gly288Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184507G>A | CA9136013 | INSR | c.783C>T (p.Asp261=) n.758C>T c.861C>T (p.Asp287=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184507G>C | CA9136014 | INSR | c.783C>G (p.Asp261Glu) n.758C>G c.861C>G (p.Asp287Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184507G= | CA2320796296 | INSR | c.783C= (p.Asp261=) n.758C= c.861C= (p.Asp287=) | |
| 19 | g.7184507G>T | CA304866609 | INSR | c.783C>A (p.Asp261Glu) n.758C>A c.861C>A (p.Asp287Glu) | dbSNP |
| 19 | g.7184508T>A | CA403670116 | INSR | c.782A>T (p.Asp261Val) n.757A>T c.860A>T (p.Asp287Val) | |
| 19 | g.7184508T>C | CA403670113 | INSR | c.782A>G (p.Asp261Gly) n.757A>G c.860A>G (p.Asp287Gly) | |
| 19 | g.7184508T>G | CA403670111 | INSR | c.782A>C (p.Asp261Ala) n.757A>C c.860A>C (p.Asp287Ala) | |
| 19 | g.7184509C>A | CA304866610 | INSR | c.781G>T (p.Asp261Tyr) n.756G>T c.859G>T (p.Asp287Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184509C= | CA2320796300 | INSR | c.781G= (p.Asp261=) n.756G= c.859G= (p.Asp287=) | |
| 19 | g.7184509C>G | CA403670120 | INSR | c.781G>C (p.Asp261His) n.756G>C c.859G>C (p.Asp287His) | |
| 19 | g.7184509C>T | CA403670122 | INSR | c.781G>A (p.Asp261Asn) n.756G>A c.859G>A (p.Asp287Asn) | dbSNP gnomAD v4 |
| 19 | g.7184510C>A | CA505400481 | INSR | c.780G>T (p.Leu260=) n.755G>T c.858G>T (p.Leu286=) | |
| 19 | g.7184510C>G | CA505400479 | INSR | c.780G>C (p.Leu260=) n.755G>C c.858G>C (p.Leu286=) | |
| 19 | g.7184510C>T | CA505400480 | INSR | c.780G>A (p.Leu260=) n.755G>A c.858G>A (p.Leu286=) | gnomAD v4 |
| 19 | g.7184511A= | CA2320796303 | INSR | c.779T= (p.Leu260=) n.754T= c.857T= (p.Leu286=) | |
| 19 | g.7184511A>C | CA403670124 | INSR | c.779T>G (p.Leu260Arg) n.754T>G c.857T>G (p.Leu286Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184511A>G | CA124227 | INSR | c.779T>C (p.Leu260Pro) n.754T>C c.857T>C (p.Leu286Pro) | ClinVar dbSNP |
| 19 | g.7184511A>T | CA403670128 | INSR | c.779T>A (p.Leu260Gln) n.754T>A c.857T>A (p.Leu286Gln) | |
| 19 | g.7184512G>A | CA505400482 | INSR | c.778C>T (p.Leu260=) n.753C>T c.856C>T (p.Leu286=) | COSMIC COSMIC |
| 19 | g.7184512G>C | CA403670131 | INSR | c.778C>G (p.Leu260Val) n.753C>G c.856C>G (p.Leu286Val) | |
| 19 | g.7184512G>T | CA403670133 | INSR | c.778C>A (p.Leu260Met) n.753C>A c.856C>A (p.Leu286Met) | gnomAD v4 |
| 19 | g.7184513G>A | CA505400483 | INSR | c.777C>T (p.Tyr259=) n.752C>T c.855C>T (p.Tyr285=) | dbSNP |
| 19 | g.7184513G>C | CA403670135 | INSR | c.777C>G (p.Tyr259Ter) n.752C>G c.855C>G (p.Tyr285Ter) | gnomAD v4 |
| 19 | g.7184513G= | CA2320796310 | INSR | c.777C= (p.Tyr259=) n.752C= c.855C= (p.Tyr285=) | |
| 19 | g.7184513G>T | CA403670138 | INSR | c.777C>A (p.Tyr259Ter) n.752C>A c.855C>A (p.Tyr285Ter) | |
| 19 | g.7184514T>A | CA403670141 | INSR | c.776A>T (p.Tyr259Phe) n.751A>T c.854A>T (p.Tyr285Phe) | |
| 19 | g.7184514T>C | CA403670142 | INSR | c.776A>G (p.Tyr259Cys) n.751A>G c.854A>G (p.Tyr285Cys) | gnomAD v4 |
| 19 | g.7184514T>G | CA403670143 | INSR | c.776A>C (p.Tyr259Ser) n.751A>C c.854A>C (p.Tyr285Ser) | |
| 19 | g.7184515A>C | CA403670150 | INSR | c.775T>G (p.Tyr259Asp) n.750T>G c.853T>G (p.Tyr285Asp) | |
| 19 | g.7184515A>G | CA403670147 | INSR | c.775T>C (p.Tyr259His) n.750T>C c.853T>C (p.Tyr285His) | |
| 19 | g.7184515A>T | CA403670145 | INSR | c.775T>A (p.Tyr259Asn) n.750T>A c.853T>A (p.Tyr285Asn) | |
| 19 | g.7184516G>A | CA505400484 | INSR | c.774C>T (p.Phe258=) n.749C>T c.852C>T (p.Phe284=) | COSMIC COSMIC |
| 19 | g.7184516G>C | CA403670153 | INSR | c.774C>G (p.Phe258Leu) n.749C>G c.852C>G (p.Phe284Leu) | |
| 19 | g.7184516G>T | CA403670154 | INSR | c.774C>A (p.Phe258Leu) n.749C>A c.852C>A (p.Phe284Leu) | |
| 19 | g.7184517A>C | CA403670158 | INSR | c.773T>G (p.Phe258Cys) n.748T>G c.851T>G (p.Phe284Cys) | |
| 19 | g.7184517A>G | CA403670160 | INSR | c.773T>C (p.Phe258Ser) n.748T>C c.851T>C (p.Phe284Ser) | COSMIC COSMIC |
| 19 | g.7184517A>T | CA403670162 | INSR | c.773T>A (p.Phe258Tyr) n.748T>A c.851T>A (p.Phe284Tyr) | |
| 19 | g.7184518A>C | CA403670166 | INSR | c.772T>G (p.Phe258Val) n.747T>G c.850T>G (p.Phe284Val) | |
| 19 | g.7184518A>G | CA403670168 | INSR | c.772T>C (p.Phe258Leu) n.747T>C c.850T>C (p.Phe284Leu) | dbSNP |
| 19 | g.7184518A>T | CA403670170 | INSR | c.772T>A (p.Phe258Ile) n.747T>A c.850T>A (p.Phe284Ile) | |
| 19 | g.7184519G>A | CA505400485 | INSR | c.771C>T (p.Asn257=) n.746C>T c.849C>T (p.Asn283=) | |
| 19 | g.7184519G>C | CA403670174 | INSR | c.771C>G (p.Asn257Lys) n.746C>G c.849C>G (p.Asn283Lys) | |
| 19 | g.7184519G>T | CA403670176 | INSR | c.771C>A (p.Asn257Lys) n.746C>A c.849C>A (p.Asn283Lys) | |
| 19 | g.7184520T>A | CA403670179 | INSR | c.770A>T (p.Asn257Ile) n.745A>T c.848A>T (p.Asn283Ile) | |
| 19 | g.7184520T>C | CA9136015 | INSR | c.770A>G (p.Asn257Ser) n.745A>G c.848A>G (p.Asn283Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184520T>G | CA403670182 | INSR | c.770A>C (p.Asn257Thr) n.745A>C c.848A>C (p.Asn283Thr) | |
| 19 | g.7184520T= | CA2320796312 | INSR | c.770A= (p.Asn257=) n.745A= c.848A= (p.Asn283=) | |
| 19 | g.7184520_7184524delinsTTGCG | CA2320796313 | INSR | c.766_770delinsCGCAA (p.Arg256=) n.741_745delinsCGCAA c.844_848delinsCGCAA (p.Arg282=) | |
| 19 | g.7184521T>A | CA403670187 | INSR | c.769A>T (p.Asn257Tyr) n.744A>T c.847A>T (p.Asn283Tyr) | |
| 19 | g.7184521T>C | CA403670189 | INSR | c.769A>G (p.Asn257Asp) n.744A>G c.847A>G (p.Asn283Asp) | |
| 19 | g.7184521T>G | CA403670185 | INSR | c.769A>C (p.Asn257His) n.744A>C c.847A>C (p.Asn283His) | |
| 19 | g.7184521_7184524del | CA884188108 | INSR | c.766_769del (p.Arg256ThrfsTer25) n.741_744del c.844_847del (p.Arg282ThrfsTer25) | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.7184522G>A | CA505400486 | INSR | c.768C>T (p.Arg256=) n.743C>T c.846C>T (p.Arg282=) | |
| 19 | g.7184522G>C | CA505400487 | INSR | c.768C>G (p.Arg256=) n.743C>G c.846C>G (p.Arg282=) | |
| 19 | g.7184522G= | CA2320796314 | INSR | c.768C= (p.Arg256=) n.743C= c.846C= (p.Arg282=) | |
| 19 | g.7184522G>T | CA505400488 | INSR | c.768C>A (p.Arg256=) n.743C>A c.846C>A (p.Arg282=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184523C>A | CA403670193 | INSR | c.767G>T (p.Arg256Leu) n.742G>T c.845G>T (p.Arg282Leu) | gnomAD v4 |
| 19 | g.7184523C= | CA2320796315 | INSR | c.767G= (p.Arg256=) n.742G= c.845G= (p.Arg282=) | |
| 19 | g.7184523C>G | CA403670194 | INSR | c.767G>C (p.Arg256Pro) n.742G>C c.845G>C (p.Arg282Pro) | gnomAD v4 |
| 19 | g.7184523C>T | CA9136016 | INSR | c.767G>A (p.Arg256His) n.742G>A c.845G>A (p.Arg282His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184523_7184524insCA | CA2580612154 | INSR | c.766_767insTG (p.Arg256LeufsTer27) n.741_742insTG c.844_845insTG (p.Arg282LeufsTer27) | |
| 19 | g.7184524G>A | CA9136017 | INSR | c.766C>T (p.Arg256Cys) n.741C>T c.844C>T (p.Arg282Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184524G>C | CA403670201 | INSR | c.766C>G (p.Arg256Gly) n.741C>G c.844C>G (p.Arg282Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184524G= | CA2320796316 | INSR | c.766C= (p.Arg256=) n.741C= c.844C= (p.Arg282=) | |
| 19 | g.7184524G>T | CA403670203 | INSR | c.766C>A (p.Arg256Ser) n.741C>A c.844C>A (p.Arg282Ser) | |
| 19 | g.7184525G>A | CA505400489 | INSR | c.765C>T (p.Cys255=) n.740C>T c.843C>T (p.Cys281=) | |
| 19 | g.7184525G>C | CA403670204 | INSR | c.765C>G (p.Cys255Trp) n.740C>G c.843C>G (p.Cys281Trp) | |
| 19 | g.7184525G>T | CA403670206 | INSR | c.765C>A (p.Cys255Ter) n.740C>A c.843C>A (p.Cys281Ter) | |
| 19 | g.7184526C>A | CA403670209 | INSR | c.764G>T (p.Cys255Phe) n.739G>T c.842G>T (p.Cys281Phe) | gnomAD v4 |
| 19 | g.7184526C>G | CA403670212 | INSR | c.764G>C (p.Cys255Ser) n.739G>C c.842G>C (p.Cys281Ser) | |
| 19 | g.7184526C>T | CA403670214 | INSR | c.764G>A (p.Cys255Tyr) n.739G>A c.842G>A (p.Cys281Tyr) | |
| 19 | g.7184527A>C | CA403670221 | INSR | c.763T>G (p.Cys255Gly) n.738T>G c.841T>G (p.Cys281Gly) | |
| 19 | g.7184527A>G | CA403670219 | INSR | c.763T>C (p.Cys255Arg) n.738T>C c.841T>C (p.Cys281Arg) | |
| 19 | g.7184527A>T | CA403670218 | INSR | c.763T>A (p.Cys255Ser) n.738T>A c.841T>A (p.Cys281Ser) | |
| 19 | g.7184528G>A | CA505400490 | INSR | c.762C>T (p.Ala254=) n.737C>T c.840C>T (p.Ala280=) | |
| 19 | g.7184528G>C | CA505400491 | INSR | c.762C>G (p.Ala254=) n.737C>G c.840C>G (p.Ala280=) | |
| 19 | g.7184528G>T | CA505400492 | INSR | c.762C>A (p.Ala254=) n.737C>A c.840C>A (p.Ala280=) | |
| 19 | g.7184529G>A | CA403670224 | INSR | c.761C>T (p.Ala254Val) n.736C>T c.839C>T (p.Ala280Val) | |
| 19 | g.7184529G>C | CA403670226 | INSR | c.761C>G (p.Ala254Gly) n.736C>G c.839C>G (p.Ala280Gly) | |
| 19 | g.7184529G>T | CA403670228 | INSR | c.761C>A (p.Ala254Asp) n.736C>A c.839C>A (p.Ala280Asp) | |
| 19 | g.7184530C>A | CA403670231 | INSR | c.760G>T (p.Ala254Ser) n.735G>T c.838G>T (p.Ala280Ser) | |
| 19 | g.7184530C>G | CA403670233 | INSR | c.760G>C (p.Ala254Pro) n.735G>C c.838G>C (p.Ala280Pro) | gnomAD v4 |
| 19 | g.7184530C>T | CA403670235 | INSR | c.760G>A (p.Ala254Thr) n.735G>A c.838G>A (p.Ala280Thr) | |
| 19 | g.7184531C>A | CA505400495 | INSR | c.759G>T (p.Val253=) n.734G>T c.837G>T (p.Val279=) | |
| 19 | g.7184531C>G | CA505400493 | INSR | c.759G>C (p.Val253=) n.734G>C c.837G>C (p.Val279=) | |
| 19 | g.7184531C>T | CA505400494 | INSR | c.759G>A (p.Val253=) n.734G>A c.837G>A (p.Val279=) | |
| 19 | g.7184532A= | CA2320796317 | INSR | c.758T= (p.Val253=) n.733T= c.836T= (p.Val279=) | |
| 19 | g.7184532A>C | CA403670238 | INSR | c.758T>G (p.Val253Gly) n.733T>G c.836T>G (p.Val279Gly) | |
| 19 | g.7184532A>G | CA403670240 | INSR | c.758T>C (p.Val253Ala) n.733T>C c.836T>C (p.Val279Ala) | |
| 19 | g.7184532A>T | CA9136018 | INSR | c.758T>A (p.Val253Glu) n.733T>A c.836T>A (p.Val279Glu) | dbSNP ExAC gnomAD v2 |
| 19 | g.7184533C>A | CA403670245 | INSR | c.757G>T (p.Val253Leu) n.732G>T c.835G>T (p.Val279Leu) | |
| 19 | g.7184533C= | CA2320796318 | INSR | c.757G= (p.Val253=) n.732G= c.835G= (p.Val279=) | |
| 19 | g.7184533C>G | CA403670247 | INSR | c.757G>C (p.Val253Leu) n.732G>C c.835G>C (p.Val279Leu) | |
| 19 | g.7184533C>T | CA403670248 | INSR | c.757G>A (p.Val253Met) n.732G>A c.835G>A (p.Val279Met) | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.7184534G>A | CA9136019 | INSR | c.756C>T (p.Cys252=) n.731C>T c.834C>T (p.Cys278=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 19 | g.7184534G>C | CA403670254 | INSR | c.756C>G (p.Cys252Trp) n.731C>G c.834C>G (p.Cys278Trp) | |
| 19 | g.7184534G= | CA2320796319 | INSR | c.756C= (p.Cys252=) n.731C= c.834C= (p.Cys278=) | |
| 19 | g.7184534G>T | CA403670251 | INSR | c.756C>A (p.Cys252Ter) n.731C>A c.834C>A (p.Cys278Ter) | |
| 19 | g.7184535C>A | CA403670256 | INSR | c.755G>T (p.Cys252Phe) n.730G>T c.833G>T (p.Cys278Phe) | |
| 19 | g.7184535C= | CA2320796320 | INSR | c.755G= (p.Cys252=) n.730G= c.833G= (p.Cys278=) | |
| 19 | g.7184535C>G | CA304866645 | INSR | c.755G>C (p.Cys252Ser) n.730G>C c.833G>C (p.Cys278Ser) | dbSNP gnomAD v4 |
| 19 | g.7184535C>T | CA403670257 | INSR | c.755G>A (p.Cys252Tyr) n.730G>A c.833G>A (p.Cys278Tyr) | gnomAD v4 |
| 19 | g.7184536A= | CA2320796321 | INSR | c.754T= (p.Cys252=) n.729T= c.832T= (p.Cys278=) | |
| 19 | g.7184536A>C | CA403670258 | INSR | c.754T>G (p.Cys252Gly) n.729T>G c.832T>G (p.Cys278Gly) | dbSNP gnomAD v2 |
| 19 | g.7184536A>G | CA403670259 | INSR | c.754T>C (p.Cys252Arg) n.729T>C c.832T>C (p.Cys278Arg) | gnomAD v4 |
| 19 | g.7184536A>T | CA403670260 | INSR | c.754T>A (p.Cys252Ser) n.729T>A c.832T>A (p.Cys278Ser) | |
| 19 | g.7184537C>A | CA403670261 | INSR | c.753G>T (p.Lys251Asn) n.728G>T c.831G>T (p.Lys277Asn) | |
| 19 | g.7184537C= | CA2320796322 | INSR | c.753G= (p.Lys251=) n.728G= c.831G= (p.Lys277=) | |
| 19 | g.7184537C>G | CA403670262 | INSR | c.753G>C (p.Lys251Asn) n.728G>C c.831G>C (p.Lys277Asn) | dbSNP |
| 19 | g.7184537C>T | CA505400496 | INSR | c.753G>A (p.Lys251=) n.728G>A c.831G>A (p.Lys277=) | gnomAD v4 |
| 19 | g.7184538T>A | CA403670263 | INSR | c.752A>T (p.Lys251Met) n.727A>T c.830A>T (p.Lys277Met) | |
| 19 | g.7184538T>C | CA403670264 | INSR | c.752A>G (p.Lys251Arg) n.727A>G c.830A>G (p.Lys277Arg) | |
| 19 | g.7184538T>G | CA403670265 | INSR | c.752A>C (p.Lys251Thr) n.727A>C c.830A>C (p.Lys277Thr) | |
| 19 | g.7184539T>A | CA403670266 | INSR | c.751A>T (p.Lys251Ter) n.726A>T c.829A>T (p.Lys277Ter) | |
| 19 | g.7184539T>C | CA403670267 | INSR | c.751A>G (p.Lys251Glu) n.726A>G c.829A>G (p.Lys277Glu) | |
| 19 | g.7184539T>G | CA403670268 | INSR | c.751A>C (p.Lys251Gln) n.726A>C c.829A>C (p.Lys277Gln) | |
| 19 | g.7184542_7184544del | CA2695228027 | INSR | c.749_751del (p.Thr250del) n.724_726del c.827_829del (p.Thr276del) | |
| 19 | g.7184540G>A | CA505400497 | INSR | c.750C>T (p.Thr250=) n.725C>T c.828C>T (p.Thr276=) | |
| 19 | g.7184540G>C | CA505400498 | INSR | c.750C>G (p.Thr250=) n.725C>G c.828C>G (p.Thr276=) | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.7184540G= | CA2320796323 | INSR | c.750C= (p.Thr250=) n.725C= c.828C= (p.Thr276=) | |
| 19 | g.7184540G>T | CA505400499 | INSR | c.750C>A (p.Thr250=) n.725C>A c.828C>A (p.Thr276=) | |
| 19 | g.7184541G>A | CA403670274 | INSR | c.749C>T (p.Thr250Ile) n.724C>T c.827C>T (p.Thr276Ile) | |
| 19 | g.7184541G>C | CA403670272 | INSR | c.749C>G (p.Thr250Ser) n.724C>G c.827C>G (p.Thr276Ser) | |
| 19 | g.7184541G>T | CA403670270 | INSR | c.749C>A (p.Thr250Asn) n.724C>A c.827C>A (p.Thr276Asn) | |
| 19 | g.7184542T>A | CA403670277 | INSR | c.748A>T (p.Thr250Ser) n.723A>T c.826A>T (p.Thr276Ser) | |
| 19 | g.7184542T>C | CA403670279 | INSR | c.748A>G (p.Thr250Ala) n.723A>G c.826A>G (p.Thr276Ala) | |
| 19 | g.7184542T>G | CA403670281 | INSR | c.748A>C (p.Thr250Pro) n.723A>C c.826A>C (p.Thr276Pro) | gnomAD v4 |
| 19 | g.7184543G>A | CA505400500 | INSR | c.747C>T (p.Pro249=) n.722C>T c.825C>T (p.Pro275=) | |
| 19 | g.7184543G>C | CA505400501 | INSR | c.747C>G (p.Pro249=) n.722C>G c.825C>G (p.Pro275=) | |
| 19 | g.7184543G= | CA2320796324 | INSR | c.747C= (p.Pro249=) n.722C= c.825C= (p.Pro275=) | |
| 19 | g.7184543G>T | CA304866646 | INSR | c.747C>A (p.Pro249=) n.722C>A c.825C>A (p.Pro275=) | dbSNP |
| 19 | g.7184544G>A | CA403670285 | INSR | c.746C>T (p.Pro249Leu) n.721C>T c.824C>T (p.Pro275Leu) | |
| 19 | g.7184544G>C | CA403670287 | INSR | c.746C>G (p.Pro249Arg) n.721C>G c.824C>G (p.Pro275Arg) | |
| 19 | g.7184544G>T | CA403670289 | INSR | c.746C>A (p.Pro249His) n.721C>A c.824C>A (p.Pro275His) | gnomAD v4 |
| 19 | g.7184545G>A | CA403670292 | INSR | c.745C>T (p.Pro249Ser) n.720C>T c.823C>T (p.Pro275Ser) | COSMIC COSMIC |
| 19 | g.7184545G>C | CA403670294 | INSR | c.745C>G (p.Pro249Ala) n.720C>G c.823C>G (p.Pro275Ala) | |
| 19 | g.7184545G>T | CA403670296 | INSR | c.745C>A (p.Pro249Thr) n.720C>A c.823C>A (p.Pro275Thr) | |
| 19 | g.7184546G>A | CA505400502 | INSR | c.744C>T (p.Asp248=) n.719C>T c.822C>T (p.Asp274=) | dbSNP gnomAD v4 |
| 19 | g.7184546G>C | CA403670299 | INSR | c.744C>G (p.Asp248Glu) n.719C>G c.822C>G (p.Asp274Glu) | |
| 19 | g.7184546G= | CA2320796325 | INSR | c.744C= (p.Asp248=) n.719C= c.822C= (p.Asp274=) | |
| 19 | g.7184546G>T | CA403670301 | INSR | c.744C>A (p.Asp248Glu) n.719C>A c.822C>A (p.Asp274Glu) | |
| 19 | g.7184547T>A | CA403670305 | INSR | c.743A>T (p.Asp248Val) n.718A>T c.821A>T (p.Asp274Val) | |
| 19 | g.7184547T>C | CA403670308 | INSR | c.743A>G (p.Asp248Gly) n.718A>G c.821A>G (p.Asp274Gly) | |
| 19 | g.7184547T>G | CA304866647 | INSR | c.743A>C (p.Asp248Ala) n.718A>C c.821A>C (p.Asp274Ala) | dbSNP |
| 19 | g.7184547T= | CA2320796326 | INSR | c.743A= (p.Asp248=) n.718A= c.821A= (p.Asp274=) | |
| 19 | g.7184548C>A | CA403670310 | INSR | c.742G>T (p.Asp248Tyr) n.717G>T c.820G>T (p.Asp274Tyr) | |
| 19 | g.7184548C= | CA2320796327 | INSR | c.742G= (p.Asp248=) n.717G= c.820G= (p.Asp274=) | |
| 19 | g.7184548C>G | CA403670313 | INSR | c.742G>C (p.Asp248His) n.717G>C c.820G>C (p.Asp274His) | |
| 19 | g.7184548C>T | CA9136020 | INSR | c.742G>A (p.Asp248Asn) n.717G>A c.820G>A (p.Asp274Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184549G>A | CA9136021 | INSR | c.741C>T (p.Asp247=) n.716C>T c.819C>T (p.Asp273=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184549G>C | CA403670318 | INSR | c.741C>G (p.Asp247Glu) n.716C>G c.819C>G (p.Asp273Glu) | |
| 19 | g.7184549G= | CA2320796328 | INSR | c.741C= (p.Asp247=) n.716C= c.819C= (p.Asp273=) | |
| 19 | g.7184549G>T | CA403670320 | INSR | c.741C>A (p.Asp247Glu) n.716C>A c.819C>A (p.Asp273Glu) | gnomAD v4 |
| 19 | g.7184550T>A | CA403670327 | INSR | c.740A>T (p.Asp247Val) n.715A>T c.818A>T (p.Asp273Val) | |
| 19 | g.7184550T>C | CA403670323 | INSR | c.740A>G (p.Asp247Gly) n.715A>G c.818A>G (p.Asp273Gly) | |
| 19 | g.7184550T>G | CA403670325 | INSR | c.740A>C (p.Asp247Ala) n.715A>C c.818A>C (p.Asp273Ala) | |
| 19 | g.7184551C>A | CA403670329 | INSR | c.739G>T (p.Asp247Tyr) n.714G>T c.817G>T (p.Asp273Tyr) | COSMIC COSMIC |
| 19 | g.7184551C= | CA2320796329 | INSR | c.739G= (p.Asp247=) n.714G= c.817G= (p.Asp273=) | |
| 19 | g.7184551C>G | CA403670331 | INSR | c.739G>C (p.Asp247His) n.714G>C c.817G>C (p.Asp273His) | |
| 19 | g.7184551C>T | CA9136022 | INSR | c.739G>A (p.Asp247Asn) n.714G>A c.817G>A (p.Asp273Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184552G>A | CA9136023 | INSR | c.738C>T (p.Pro246=) n.713C>T c.816C>T (p.Pro272=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 19 | g.7184552G>C | CA9136024 | INSR | c.738C>G (p.Pro246=) n.713C>G c.816C>G (p.Pro272=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184552G= | CA2320796330 | INSR | c.738C= (p.Pro246=) n.713C= c.816C= (p.Pro272=) | |
| 19 | g.7184552G>T | CA505400503 | INSR | c.738C>A (p.Pro246=) n.713C>A c.816C>A (p.Pro272=) | |
| 19 | g.7184553_7184554del | CA2813464193 | INSR | c.737_738del (p.Pro246ArgfsTer?) n.712_713del c.815_816del (p.Pro272ArgfsTer?) | |
| 19 | g.7184553G>A | CA9136025 | INSR | c.737C>T (p.Pro246Leu) n.712C>T c.815C>T (p.Pro272Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184553G>C | CA403670342 | INSR | c.737C>G (p.Pro246Arg) n.712C>G c.815C>G (p.Pro272Arg) | |
| 19 | g.7184553G= | CA2320796331 | INSR | c.737C= (p.Pro246=) n.712C= c.815C= (p.Pro272=) | |
| 19 | g.7184553G>T | CA403670340 | INSR | c.737C>A (p.Pro246His) n.712C>A c.815C>A (p.Pro272His) | |
| 19 | g.7184554G>A | CA403670345 | INSR | c.736C>T (p.Pro246Ser) n.711C>T c.814C>T (p.Pro272Ser) | gnomAD v4 |
| 19 | g.7184554G>C | CA403670348 | INSR | c.736C>G (p.Pro246Ala) n.711C>G c.814C>G (p.Pro272Ala) | |
| 19 | g.7184554G= | CA2320796332 | INSR | c.736C= (p.Pro246=) n.711C= c.814C= (p.Pro272=) | |
| 19 | g.7184554G>T | CA403670349 | INSR | c.736C>A (p.Pro246Thr) n.711C>A c.814C>A (p.Pro272Thr) | dbSNP gnomAD v4 |
| 19 | g.7184555C>A | CA403670352 | INSR | c.735G>T (p.Gln245His) n.710G>T c.813G>T (p.Gln271His) | |
| 19 | g.7184555C>G | CA403670355 | INSR | c.735G>C (p.Gln245His) n.710G>C c.813G>C (p.Gln271His) | |
| 19 | g.7184555C>T | CA505400504 | INSR | c.735G>A (p.Gln245=) n.710G>A c.813G>A (p.Gln271=) | |
| 19 | g.7184556T>A | CA403670358 | INSR | c.734A>T (p.Gln245Leu) n.709A>T c.812A>T (p.Gln271Leu) | |
| 19 | g.7184556T>C | CA9136026 | INSR | c.734A>G (p.Gln245Arg) n.709A>G c.812A>G (p.Gln271Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184556T>G | CA403670361 | INSR | c.734A>C (p.Gln245Pro) n.709A>C c.812A>C (p.Gln271Pro) | |
| 19 | g.7184556T= | CA2320796333 | INSR | c.734A= (p.Gln245=) n.709A= c.812A= (p.Gln271=) | |
| 19 | g.7184557G>A | CA403670364 | INSR | c.733C>T (p.Gln245Ter) n.708C>T c.811C>T (p.Gln271Ter) | COSMIC COSMIC |
| 19 | g.7184557G>C | CA403670366 | INSR | c.733C>G (p.Gln245Glu) n.708C>G c.811C>G (p.Gln271Glu) | |
| 19 | g.7184557G>T | CA403670368 | INSR | c.733C>A (p.Gln245Lys) n.708C>A c.811C>A (p.Gln271Lys) | |
| 19 | g.7184558A>C | CA505400506 | INSR | c.732T>G (p.Ser244=) n.707T>G c.810T>G (p.Ser270=) | |
| 19 | g.7184558A>G | CA505400507 | INSR | c.732T>C (p.Ser244=) n.707T>C c.810T>C (p.Ser270=) | |
| 19 | g.7184558A>T | CA505400505 | INSR | c.732T>A (p.Ser244=) n.707T>A c.810T>A (p.Ser270=) | |
| 19 | g.7184559G>A | CA403670375 | INSR | c.731C>T (p.Ser244Phe) n.706C>T c.809C>T (p.Ser270Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184559G>C | CA403670373 | INSR | c.731C>G (p.Ser244Cys) n.706C>G c.809C>G (p.Ser270Cys) | |
| 19 | g.7184559G= | CA2320796334 | INSR | c.731C= (p.Ser244=) n.706C= c.809C= (p.Ser270=) | |
| 19 | g.7184559G>T | CA403670371 | INSR | c.731C>A (p.Ser244Tyr) n.706C>A c.809C>A (p.Ser270Tyr) | |
| 19 | g.7184560A>C | CA403670379 | INSR | c.730T>G (p.Ser244Ala) n.705T>G c.808T>G (p.Ser270Ala) | |
| 19 | g.7184560A>G | CA403670383 | INSR | c.730T>C (p.Ser244Pro) n.705T>C c.808T>C (p.Ser270Pro) | gnomAD v4 |
| 19 | g.7184560A>T | CA403670381 | INSR | c.730T>A (p.Ser244Thr) n.705T>A c.808T>A (p.Ser270Thr) | |
| 19 | g.7184561A>C | CA403670386 | INSR | c.729T>G (p.Cys243Trp) n.704T>G c.807T>G (p.Cys269Trp) | |
| 19 | g.7184561A>G | CA505400508 | INSR | c.729T>C (p.Cys243=) n.704T>C c.807T>C (p.Cys269=) | |
| 19 | g.7184561A>T | CA403670388 | INSR | c.729T>A (p.Cys243Ter) n.704T>A c.807T>A (p.Cys269Ter) | |
| 19 | g.7184562C>A | CA403670391 | INSR | c.728G>T (p.Cys243Phe) n.703G>T c.806G>T (p.Cys269Phe) | |
| 19 | g.7184562C= | CA2320796335 | INSR | c.728G= (p.Cys243=) n.703G= c.806G= (p.Cys269=) | |
| 19 | g.7184562C>G | CA403670393 | INSR | c.728G>C (p.Cys243Ser) n.703G>C c.806G>C (p.Cys269Ser) | |
| 19 | g.7184562C>T | CA304866660 | INSR | c.728G>A (p.Cys243Tyr) n.703G>A c.806G>A (p.Cys269Tyr) | ClinVar dbSNP |
| 19 | g.7184563A= | CA2320796336 | INSR | c.727T= (p.Cys243=) n.702T= c.805T= (p.Cys269=) | |
| 19 | g.7184563A>C | CA403670397 | INSR | c.727T>G (p.Cys243Gly) n.702T>G c.805T>G (p.Cys269Gly) | dbSNP |
| 19 | g.7184563A>G | CA403670399 | INSR | c.727T>C (p.Cys243Arg) n.702T>C c.805T>C (p.Cys269Arg) | |
| 19 | g.7184563A>T | CA403670401 | INSR | c.727T>A (p.Cys243Ser) n.702T>A c.805T>A (p.Cys269Ser) | |
| 19 | g.7184564G>A | CA505400509 | INSR | c.726C>T (p.Asn242=) n.701C>T c.804C>T (p.Asn268=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184564G>C | CA403670404 | INSR | c.726C>G (p.Asn242Lys) n.701C>G c.804C>G (p.Asn268Lys) | |
| 19 | g.7184564G= | CA2320796337 | INSR | c.726C= (p.Asn242=) n.701C= c.804C= (p.Asn268=) | |
| 19 | g.7184564G>T | CA403670406 | INSR | c.726C>A (p.Asn242Lys) n.701C>A c.804C>A (p.Asn268Lys) | |
| 19 | g.7184565T>A | CA403670409 | INSR | c.725A>T (p.Asn242Ile) n.700A>T c.803A>T (p.Asn268Ile) | |
| 19 | g.7184565T>C | CA403670411 | INSR | c.725A>G (p.Asn242Ser) n.700A>G c.803A>G (p.Asn268Ser) | |
| 19 | g.7184565T>G | CA403670413 | INSR | c.725A>C (p.Asn242Thr) n.700A>C c.803A>C (p.Asn268Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184565T= | CA2320796338 | INSR | c.725A= (p.Asn242=) n.700A= c.803A= (p.Asn268=) | |
| 19 | g.7184566T>A | CA403670415 | INSR | c.724A>T (p.Asn242Tyr) n.699A>T c.802A>T (p.Asn268Tyr) | |
| 19 | g.7184566T>C | CA403670420 | INSR | c.724A>G (p.Asn242Asp) n.699A>G c.802A>G (p.Asn268Asp) | |
| 19 | g.7184566T>G | CA403670417 | INSR | c.724A>C (p.Asn242His) n.699A>C c.802A>C (p.Asn268His) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184566T= | CA2320796339 | INSR | c.724A= (p.Asn242=) n.699A= c.802A= (p.Asn268=) | |
| 19 | g.7184567G>A | CA505400510 | INSR | c.723C>T (p.Gly241=) n.698C>T c.801C>T (p.Gly267=) | gnomAD v4 |
| 19 | g.7184567G>C | CA505400511 | INSR | c.723C>G (p.Gly241=) n.698C>G c.801C>G (p.Gly267=) | |
| 19 | g.7184567G>T | CA505400512 | INSR | c.723C>A (p.Gly241=) n.698C>A c.801C>A (p.Gly267=) | |
| 19 | g.7184568C>A | CA403670423 | INSR | c.722G>T (p.Gly241Val) n.697G>T c.800G>T (p.Gly267Val) | |
| 19 | g.7184568C>G | CA403670425 | INSR | c.722G>C (p.Gly241Ala) n.697G>C c.800G>C (p.Gly267Ala) | |
| 19 | g.7184568C>T | CA403670433 | INSR | c.722G>A (p.Gly241Asp) n.697G>A c.800G>A (p.Gly267Asp) | |
| 19 | g.7184569C>A | CA403670436 | INSR | c.721G>T (p.Gly241Cys) n.696G>T c.799G>T (p.Gly267Cys) | |
| 19 | g.7184569C>G | CA403670438 | INSR | c.721G>C (p.Gly241Arg) n.696G>C c.799G>C (p.Gly267Arg) | |
| 19 | g.7184569C>T | CA403670440 | INSR | c.721G>A (p.Gly241Ser) n.696G>A c.799G>A (p.Gly267Ser) | |
| 19 | g.7184570C>A | CA505400513 | INSR | c.720G>T (p.Leu240=) n.695G>T c.798G>T (p.Leu266=) | |
| 19 | g.7184570C>G | CA505400514 | INSR | c.720G>C (p.Leu240=) n.695G>C c.798G>C (p.Leu266=) | |
| 19 | g.7184570C>T | CA505400515 | INSR | c.720G>A (p.Leu240=) n.695G>A c.798G>A (p.Leu266=) | |
| 19 | g.7184571A= | CA2320796340 | INSR | c.719T= (p.Leu240=) n.694T= c.797T= (p.Leu266=) | |
| 19 | g.7184571A>C | CA403670444 | INSR | c.719T>G (p.Leu240Arg) n.694T>G c.797T>G (p.Leu266Arg) | |
| 19 | g.7184571A>G | CA403670446 | INSR | c.719T>C (p.Leu240Pro) n.694T>C c.797T>C (p.Leu266Pro) | dbSNP |
| 19 | g.7184571A>T | CA403670448 | INSR | c.719T>A (p.Leu240Gln) n.694T>A c.797T>A (p.Leu266Gln) | |
| 19 | g.7184572G>A | CA505400516 | INSR | c.718C>T (p.Leu240=) n.693C>T c.796C>T (p.Leu266=) | |
| 19 | g.7184572G>C | CA403670450 | INSR | c.718C>G (p.Leu240Val) n.693C>G c.796C>G (p.Leu266Val) | |
| 19 | g.7184572G>T | CA403670451 | INSR | c.718C>A (p.Leu240Met) n.693C>A c.796C>A (p.Leu266Met) | |
| 19 | g.7184573G>A | CA505400517 | INSR | c.717C>T (p.Cys239=) n.692C>T c.795C>T (p.Cys265=) | |
| 19 | g.7184573G>C | CA403670454 | INSR | c.717C>G (p.Cys239Trp) n.692C>G c.795C>G (p.Cys265Trp) | |
| 19 | g.7184573G>T | CA403670455 | INSR | c.717C>A (p.Cys239Ter) n.692C>A c.795C>A (p.Cys265Ter) | |
| 19 | g.7184574C>A | CA403670459 | INSR | c.716G>T (p.Cys239Phe) n.691G>T c.794G>T (p.Cys265Phe) | |
| 19 | g.7184574C>G | CA403670460 | INSR | c.716G>C (p.Cys239Ser) n.691G>C c.794G>C (p.Cys265Ser) | |
| 19 | g.7184574C>T | CA403670462 | INSR | c.716G>A (p.Cys239Tyr) n.691G>A c.794G>A (p.Cys265Tyr) | |
| 19 | g.7184575A>C | CA403670464 | INSR | c.715T>G (p.Cys239Gly) n.690T>G c.793T>G (p.Cys265Gly) | |
| 19 | g.7184575A>G | CA403670467 | INSR | c.715T>C (p.Cys239Arg) n.690T>C c.793T>C (p.Cys265Arg) | |
| 19 | g.7184575A>T | CA403670469 | INSR | c.715T>A (p.Cys239Ser) n.690T>A c.793T>A (p.Cys265Ser) | |
| 19 | g.7184575_7184576delinsAC | CA2320796341 | INSR | c.714_715delinsGT (p.Glu238=) n.689_690delinsGT c.792_793delinsGT (p.Glu264=) | |
| 19 | g.7184576del | CA993124683 | INSR | c.714del (p.Glu238AspfsTer?) n.689del c.792del (p.Glu264AspfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.7184576C>A | CA403670474 | INSR | c.714G>T (p.Glu238Asp) n.689G>T c.792G>T (p.Glu264Asp) | |
| 19 | g.7184576C>G | CA403670472 | INSR | c.714G>C (p.Glu238Asp) n.689G>C c.792G>C (p.Glu264Asp) | |
| 19 | g.7184576C>T | CA505400518 | INSR | c.714G>A (p.Glu238=) n.689G>A c.792G>A (p.Glu264=) | |
| 19 | g.7184577T>A | CA403670477 | INSR | c.713A>T (p.Glu238Val) n.688A>T c.791A>T (p.Glu264Val) | |
| 19 | g.7184577T>C | CA403670479 | INSR | c.713A>G (p.Glu238Gly) n.688A>G c.791A>G (p.Glu264Gly) | |
| 19 | g.7184577T>G | CA403670481 | INSR | c.713A>C (p.Glu238Ala) n.688A>C c.791A>C (p.Glu264Ala) | |
| 19 | g.7184578C>A | CA403670484 | INSR | c.712G>T (p.Glu238Ter) n.687G>T c.790G>T (p.Glu264Ter) | |
| 19 | g.7184578C= | CA2320796342 | INSR | c.712G= (p.Glu238=) n.687G= c.790G= (p.Glu264=) | |
| 19 | g.7184578C>G | CA403670486 | INSR | c.712G>C (p.Glu238Gln) n.687G>C c.790G>C (p.Glu264Gln) | |
| 19 | g.7184578C>T | CA9136027 | INSR | c.712G>A (p.Glu238Lys) n.687G>A c.790G>A (p.Glu264Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184579G>A | CA9136028 | INSR | c.711C>T (p.Ser237=) n.686C>T c.789C>T (p.Ser263=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184579G>C | CA403670492 | INSR | c.711C>G (p.Ser237Arg) n.686C>G c.789C>G (p.Ser263Arg) | |
| 19 | g.7184579G= | CA2320796343 | INSR | c.711C= (p.Ser237=) n.686C= c.789C= (p.Ser263=) | |
| 19 | g.7184579G>T | CA304866673 | INSR | c.711C>A (p.Ser237Arg) n.686C>A c.789C>A (p.Ser263Arg) | dbSNP |
| 19 | g.7184580C>A | CA403670493 | INSR | c.710G>T (p.Ser237Ile) n.685G>T c.788G>T (p.Ser263Ile) | |
| 19 | g.7184580C= | CA2320796344 | INSR | c.710G= (p.Ser237=) n.685G= c.788G= (p.Ser263=) | |
| 19 | g.7184580C>G | CA403670495 | INSR | c.710G>C (p.Ser237Thr) n.685G>C c.788G>C (p.Ser263Thr) | |
| 19 | g.7184580C>T | CA403670497 | INSR | c.710G>A (p.Ser237Asn) n.685G>A c.788G>A (p.Ser263Asn) | dbSNP |
| 19 | g.7184581T>A | CA403670502 | INSR | c.709A>T (p.Ser237Cys) n.684A>T c.787A>T (p.Ser263Cys) | |
| 19 | g.7184581T>C | CA403670504 | INSR | c.709A>G (p.Ser237Gly) n.684A>G c.787A>G (p.Ser263Gly) | |
| 19 | g.7184581T>G | CA403670507 | INSR | c.709A>C (p.Ser237Arg) n.684A>C c.787A>C (p.Ser263Arg) | |
| 19 | g.7184582G>A | CA505400519 | INSR | c.708C>T (p.His236=) n.683C>T c.786C>T (p.His262=) | gnomAD v4 |
| 19 | g.7184582G>C | CA403670509 | INSR | c.708C>G (p.His236Gln) n.683C>G c.786C>G (p.His262Gln) | |
| 19 | g.7184582G>T | CA403670511 | INSR | c.708C>A (p.His236Gln) n.683C>A c.786C>A (p.His262Gln) | |
| 19 | g.7184583T>A | CA403670514 | INSR | c.707A>T (p.His236Leu) n.682A>T c.785A>T (p.His262Leu) | |
| 19 | g.7184583T>C | CA124236 | INSR | c.707A>G (p.His236Arg) n.682A>G c.785A>G (p.His262Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7184583T>G | CA403670518 | INSR | c.707A>C (p.His236Pro) n.682A>C c.785A>C (p.His262Pro) | |
| 19 | g.7184583T= | CA2320796345 | INSR | c.707A= (p.His236=) n.682A= c.785A= (p.His262=) | |
| 19 | g.7184584G>A | CA403670523 | INSR | c.706C>T (p.His236Tyr) n.681C>T c.784C>T (p.His262Tyr) | |
| 19 | g.7184584G>C | CA403670524 | INSR | c.706C>G (p.His236Asp) n.681C>G c.784C>G (p.His262Asp) | |
| 19 | g.7184584G>T | CA403670521 | INSR | c.706C>A (p.His236Asn) n.681C>A c.784C>A (p.His262Asn) | |
| 19 | g.7184585G>A | CA9136029 | INSR | c.705C>T (p.Cys235=) n.680C>T c.783C>T (p.Cys261=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7184585G>C | CA403670528 | INSR | c.705C>G (p.Cys235Trp) n.680C>G c.783C>G (p.Cys261Trp) | |
| 19 | g.7184585G= | CA2320796346 | INSR | c.705C= (p.Cys235=) n.680C= c.783C= (p.Cys261=) | |
| 19 | g.7184585G>T | CA403670529 | INSR | c.705C>A (p.Cys235Ter) n.680C>A c.783C>A (p.Cys261Ter) | gnomAD v4 |
| 19 | g.7184586C>A | CA403670533 | INSR | c.704G>T (p.Cys235Phe) n.679G>T c.782G>T (p.Cys261Phe) | ClinVar gnomAD v4 |
| 19 | g.7184586C>G | CA403670535 | INSR | c.704G>C (p.Cys235Ser) n.679G>C c.782G>C (p.Cys261Ser) | |
| 19 | g.7184586C>T | CA403670537 | INSR | c.704G>A (p.Cys235Tyr) n.679G>A c.782G>A (p.Cys261Tyr) | |
| 19 | g.7184587A>C | CA403670541 | INSR | c.703T>G (p.Cys235Gly) n.678T>G c.781T>G (p.Cys261Gly) | |
| 19 | g.7184587A>G | CA403670543 | INSR | c.703T>C (p.Cys235Arg) n.678T>C c.781T>C (p.Cys261Arg) | |
| 19 | g.7184587A>T | CA403670545 | INSR | c.703T>A (p.Cys235Ser) n.678T>A c.781T>A (p.Cys261Ser) | |
| 19 | g.7184588A>C | CA403670547 | INSR | c.702T>G (p.Cys234Trp) n.677T>G c.780T>G (p.Cys260Trp) | gnomAD v4 |
| 19 | g.7184588A>G | CA505400520 | INSR | c.702T>C (p.Cys234=) n.677T>C c.780T>C (p.Cys260=) | |
| 19 | g.7184588A>T | CA403670549 | INSR | c.702T>A (p.Cys234Ter) n.677T>A c.780T>A (p.Cys260Ter) |