Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |