| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.7143065C>A | CA403662760 | INSR | c.2293G>T (p.Gly765Cys) c.2257G>T (p.Gly753Cys) c.2371G>T (p.Gly791Cys) c.2335G>T (p.Gly779Cys) | |
| 19 | g.7143065C= | CA2320776129 | INSR | c.2293G= (p.Gly765=) c.2257G= (p.Gly753=) c.2371G= (p.Gly791=) c.2335G= (p.Gly779=) | |
| 19 | g.7143065C>G | CA403662761 | INSR | c.2293G>C (p.Gly765Arg) c.2257G>C (p.Gly753Arg) c.2371G>C (p.Gly791Arg) c.2335G>C (p.Gly779Arg) | |
| 19 | g.7143065C>T | CA206380 | INSR | c.2293G>A (p.Gly765Ser) c.2257G>A (p.Gly753Ser) c.2371G>A (p.Gly791Ser) c.2335G>A (p.Gly779Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7143066A>C | CA505400437 | INSR | c.2292T>G (p.Leu764=) c.2256T>G (p.Leu752=) c.2370T>G (p.Leu790=) c.2334T>G (p.Leu778=) | |
| 19 | g.7143066A>G | CA505400438 | INSR | c.2292T>C (p.Leu764=) c.2256T>C (p.Leu752=) c.2370T>C (p.Leu790=) c.2334T>C (p.Leu778=) | |
| 19 | g.7143066A>T | CA505400439 | INSR | c.2292T>A (p.Leu764=) c.2256T>A (p.Leu752=) c.2370T>A (p.Leu790=) c.2334T>A (p.Leu778=) | |
| 19 | g.7143067A>C | CA403662762 | INSR | c.2291T>G (p.Leu764Arg) c.2255T>G (p.Leu752Arg) c.2369T>G (p.Leu790Arg) c.2333T>G (p.Leu778Arg) | |
| 19 | g.7143067A>G | CA403662763 | INSR | c.2291T>C (p.Leu764Pro) c.2255T>C (p.Leu752Pro) c.2369T>C (p.Leu790Pro) c.2333T>C (p.Leu778Pro) | |
| 19 | g.7143067A>T | CA403662764 | INSR | c.2291T>A (p.Leu764His) c.2255T>A (p.Leu752His) c.2369T>A (p.Leu790His) c.2333T>A (p.Leu778His) | |
| 19 | g.7143068G>A | CA304837901 | INSR | c.2290C>T (p.Leu764Phe) c.2254C>T (p.Leu752Phe) c.2368C>T (p.Leu790Phe) c.2332C>T (p.Leu778Phe) | dbSNP |
| 19 | g.7143068G>C | CA403662765 | INSR | c.2290C>G (p.Leu764Val) c.2254C>G (p.Leu752Val) c.2368C>G (p.Leu790Val) c.2332C>G (p.Leu778Val) | |
| 19 | g.7143068G= | CA2320776131 | INSR | c.2290C= (p.Leu764=) c.2254C= (p.Leu752=) c.2368C= (p.Leu790=) c.2332C= (p.Leu778=) | |
| 19 | g.7143068G>T | CA403662766 | INSR | c.2290C>A (p.Leu764Ile) c.2254C>A (p.Leu752Ile) c.2368C>A (p.Leu790Ile) c.2332C>A (p.Leu778Ile) | |
| 19 | g.7143069G>A | CA505400440 | INSR | c.2289C>T (p.Ser763=) c.2253C>T (p.Ser751=) c.2367C>T (p.Ser789=) c.2331C>T (p.Ser777=) | |
| 19 | g.7143069G>C | CA505400441 | INSR | c.2289C>G (p.Ser763=) c.2253C>G (p.Ser751=) c.2367C>G (p.Ser789=) c.2331C>G (p.Ser777=) | |
| 19 | g.7143069G>T | CA505400442 | INSR | c.2289C>A (p.Ser763=) c.2253C>A (p.Ser751=) c.2367C>A (p.Ser789=) c.2331C>A (p.Ser777=) | |
| 19 | g.7143070G>A | CA403662769 | INSR | c.2288C>T (p.Ser763Phe) c.2252C>T (p.Ser751Phe) c.2366C>T (p.Ser789Phe) c.2330C>T (p.Ser777Phe) | COSMIC COSMIC |
| 19 | g.7143070G>C | CA403662768 | INSR | c.2288C>G (p.Ser763Cys) c.2252C>G (p.Ser751Cys) c.2366C>G (p.Ser789Cys) c.2330C>G (p.Ser777Cys) | |
| 19 | g.7143070G>T | CA403662767 | INSR | c.2288C>A (p.Ser763Tyr) c.2252C>A (p.Ser751Tyr) c.2366C>A (p.Ser789Tyr) c.2330C>A (p.Ser777Tyr) | |
| 19 | g.7143071A>C | CA403662770 | INSR | c.2287T>G (p.Ser763Ala) c.2251T>G (p.Ser751Ala) c.2365T>G (p.Ser789Ala) c.2329T>G (p.Ser777Ala) | |
| 19 | g.7143071A>G | CA403662771 | INSR | c.2287T>C (p.Ser763Pro) c.2251T>C (p.Ser751Pro) c.2365T>C (p.Ser789Pro) c.2329T>C (p.Ser777Pro) | |
| 19 | g.7143071A>T | CA403662772 | INSR | c.2287T>A (p.Ser763Thr) c.2251T>A (p.Ser751Thr) c.2365T>A (p.Ser789Thr) c.2329T>A (p.Ser777Thr) | |
| 19 | g.7143072C>A | CA124221 | INSR | c.2286G>T (p.Arg762Ser) c.2250G>T (p.Arg750Ser) c.2364G>T (p.Arg788Ser) c.2328G>T (p.Arg776Ser) | ClinVar dbSNP |
| 19 | g.7143072C= | CA2320776134 | INSR | c.2286G= (p.Arg762=) c.2250G= (p.Arg750=) c.2364G= (p.Arg788=) c.2328G= (p.Arg776=) | |
| 19 | g.7143072C>G | CA403662773 | INSR | c.2286G>C (p.Arg762Ser) c.2250G>C (p.Arg750Ser) c.2364G>C (p.Arg788Ser) c.2328G>C (p.Arg776Ser) | |
| 19 | g.7143072C>T | CA505400444 | INSR | c.2286G>A (p.Arg762=) c.2250G>A (p.Arg750=) c.2364G>A (p.Arg788=) c.2328G>A (p.Arg776=) | |
| 19 | g.7143073C>A | CA403662774 | INSR | c.2285G>T (p.Arg762Met) c.2249G>T (p.Arg750Met) c.2363G>T (p.Arg788Met) c.2327G>T (p.Arg776Met) | |
| 19 | g.7143073C>G | CA403662775 | INSR | c.2285G>C (p.Arg762Thr) c.2249G>C (p.Arg750Thr) c.2363G>C (p.Arg788Thr) c.2327G>C (p.Arg776Thr) | |
| 19 | g.7143073C>T | CA403662776 | INSR | c.2285G>A (p.Arg762Lys) c.2249G>A (p.Arg750Lys) c.2363G>A (p.Arg788Lys) c.2327G>A (p.Arg776Lys) | |
| 19 | g.7143074T>A | CA403662777 | INSR | c.2284A>T (p.Arg762Trp) c.2248A>T (p.Arg750Trp) c.2362A>T (p.Arg788Trp) c.2326A>T (p.Arg776Trp) | |
| 19 | g.7143074T>C | CA403662778 | INSR | c.2284A>G (p.Arg762Gly) c.2248A>G (p.Arg750Gly) c.2362A>G (p.Arg788Gly) c.2326A>G (p.Arg776Gly) | COSMIC COSMIC |
| 19 | g.7143074T>G | CA505400445 | INSR | c.2284A>C (p.Arg762=) c.2248A>C (p.Arg750=) c.2362A>C (p.Arg788=) c.2326A>C (p.Arg776=) | |
| 19 | g.7143075G>A | CA505400448 | INSR | c.2283C>T (p.Arg761=) c.2247C>T (p.Arg749=) c.2361C>T (p.Arg787=) c.2325C>T (p.Arg775=) | gnomAD v4 |
| 19 | g.7143075G>C | CA505400446 | INSR | c.2283C>G (p.Arg761=) c.2247C>G (p.Arg749=) c.2361C>G (p.Arg787=) c.2325C>G (p.Arg775=) | |
| 19 | g.7143075G>T | CA505400447 | INSR | c.2283C>A (p.Arg761=) c.2247C>A (p.Arg749=) c.2361C>A (p.Arg787=) c.2325C>A (p.Arg775=) | |
| 19 | g.7143076C>A | CA403662779 | INSR | c.2282G>T (p.Arg761Leu) c.2246G>T (p.Arg749Leu) c.2360G>T (p.Arg787Leu) c.2324G>T (p.Arg775Leu) | |
| 19 | g.7143076C>G | CA403662780 | INSR | c.2282G>C (p.Arg761Pro) c.2246G>C (p.Arg749Pro) c.2360G>C (p.Arg787Pro) c.2324G>C (p.Arg775Pro) | |
| 19 | g.7143076C>T | CA403662781 | INSR | c.2282G>A (p.Arg761His) c.2246G>A (p.Arg749His) c.2360G>A (p.Arg787His) c.2324G>A (p.Arg775His) | gnomAD v4 |
| 19 | g.7143077G>A | CA403662783 | INSR | c.2281C>T (p.Arg761Cys) c.2245C>T (p.Arg749Cys) c.2359C>T (p.Arg787Cys) c.2323C>T (p.Arg775Cys) | gnomAD v4 |
| 19 | g.7143077G>C | CA403662784 | INSR | c.2281C>G (p.Arg761Gly) c.2245C>G (p.Arg749Gly) c.2359C>G (p.Arg787Gly) c.2323C>G (p.Arg775Gly) | |
| 19 | g.7143077G>T | CA403662782 | INSR | c.2281C>A (p.Arg761Ser) c.2245C>A (p.Arg749Ser) c.2359C>A (p.Arg787Ser) c.2323C>A (p.Arg775Ser) | |
| 19 | g.7143078T>A | CA403662785 | INSR | c.2280A>T (p.Lys760Asn) c.2244A>T (p.Lys748Asn) c.2358A>T (p.Lys786Asn) c.2322A>T (p.Lys774Asn) | |
| 19 | g.7143078T>C | CA9135586 | INSR | c.2280A>G (p.Lys760=) c.2244A>G (p.Lys748=) c.2358A>G (p.Lys786=) c.2322A>G (p.Lys774=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 19 | g.7143078T>G | CA403662786 | INSR | c.2280A>C (p.Lys760Asn) c.2244A>C (p.Lys748Asn) c.2358A>C (p.Lys786Asn) c.2322A>C (p.Lys774Asn) | |
| 19 | g.7143078T= | CA2320776136 | INSR | c.2280A= (p.Lys760=) c.2244A= (p.Lys748=) c.2358A= (p.Lys786=) c.2322A= (p.Lys774=) | |
| 19 | g.7143079T>A | CA403662787 | INSR | c.2279A>T (p.Lys760Ile) c.2243A>T (p.Lys748Ile) c.2357A>T (p.Lys786Ile) c.2321A>T (p.Lys774Ile) | |
| 19 | g.7143079T>C | CA403662788 | INSR | c.2279A>G (p.Lys760Arg) c.2243A>G (p.Lys748Arg) c.2357A>G (p.Lys786Arg) c.2321A>G (p.Lys774Arg) | |
| 19 | g.7143079T>G | CA403662789 | INSR | c.2279A>C (p.Lys760Thr) c.2243A>C (p.Lys748Thr) c.2357A>C (p.Lys786Thr) c.2321A>C (p.Lys774Thr) | |
| 19 | g.7143080T>A | CA403662790 | INSR | c.2278A>T (p.Lys760Ter) c.2242A>T (p.Lys748Ter) c.2356A>T (p.Lys786Ter) c.2320A>T (p.Lys774Ter) |