Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174674A=CA1708918248EGFRc.2185-48A= (p.=)
c.*28+1746A= (p.=)
c.2050-48A= (p.=)
c.2026-48A= (p.=)
c.1384-48A= (p.=)
7g.55174674A>GCA1708918249EGFRc.2185-48A>G (p.=)
c.*28+1746A>G (p.=)
c.2050-48A>G (p.=)
c.2026-48A>G (p.=)
c.1384-48A>G (p.=)
7g.55174675C=CA1708918250EGFRc.2185-47C= (p.=)
c.*28+1747C= (p.=)
c.2050-47C= (p.=)
c.2026-47C= (p.=)
c.1384-47C= (p.=)
7g.55174675C>TCA839813217EGFRc.2185-47C>T (p.=)
c.*28+1747C>T (p.=)
c.2050-47C>T (p.=)
c.2026-47C>T (p.=)
c.1384-47C>T (p.=)
7g.55174676C=CA1708918251EGFRc.2185-46C= (p.=)
c.*28+1748C= (p.=)
c.2050-46C= (p.=)
c.2026-46C= (p.=)
c.1384-46C= (p.=)
7g.55174676C>TCA1101518203EGFRc.2185-46C>T (p.=)
c.*28+1748C>T (p.=)
c.2050-46C>T (p.=)
c.2026-46C>T (p.=)
c.1384-46C>T (p.=)
7g.55174677A=CA1708918252EGFRc.2185-45A= (p.=)
c.*28+1749A= (p.=)
c.2050-45A= (p.=)
c.2026-45A= (p.=)
c.1384-45A= (p.=)
7g.55174677A>GCA574335556EGFRc.2185-45A>G (p.=)
c.*28+1749A>G (p.=)
c.2050-45A>G (p.=)
c.2026-45A>G (p.=)
c.1384-45A>G (p.=)
gnomAD
7g.55174683C=CA1708918253EGFRc.2185-39C= (p.=)
c.*28+1755C= (p.=)
c.2050-39C= (p.=)
c.2026-39C= (p.=)
c.1384-39C= (p.=)
7g.55174683C>TCA1708918254EGFRc.2185-39C>T (p.=)
c.*28+1755C>T (p.=)
c.2050-39C>T (p.=)
c.2026-39C>T (p.=)
c.1384-39C>T (p.=)
7g.55174684A=CA1708918255EGFRc.2185-38A= (p.=)
c.*28+1756A= (p.=)
c.2050-38A= (p.=)
c.2026-38A= (p.=)
c.1384-38A= (p.=)
7g.55174684A>CCA1708918256EGFRc.2185-38A>C (p.=)
c.*28+1756A>C (p.=)
c.2050-38A>C (p.=)
c.2026-38A>C (p.=)
c.1384-38A>C (p.=)
7g.55174685A=CA1708918257EGFRc.2185-37A= (p.=)
c.*28+1757A= (p.=)
c.2050-37A= (p.=)
c.2026-37A= (p.=)
c.1384-37A= (p.=)
7g.55174685A>GCA4266002EGFRc.2185-37A>G (p.=)
c.*28+1757A>G (p.=)
c.2050-37A>G (p.=)
c.2026-37A>G (p.=)
c.1384-37A>G (p.=)
dbSNP ExAC gnomAD
7g.55174686T>CCA1708918259EGFRc.2185-36T>C (p.=)
c.*28+1758T>C (p.=)
c.2050-36T>C (p.=)
c.2026-36T>C (p.=)
c.1384-36T>C (p.=)
7g.55174686T=CA1708918258EGFRc.2185-36T= (p.=)
c.*28+1758T= (p.=)
c.2050-36T= (p.=)
c.2026-36T= (p.=)
c.1384-36T= (p.=)
7g.55174687T>ACA574335559EGFRc.2185-35T>A (p.=)
c.*28+1759T>A (p.=)
c.2050-35T>A (p.=)
c.2026-35T>A (p.=)
c.1384-35T>A (p.=)
gnomAD
7g.55174687T=CA1708918260EGFRc.2185-35T= (p.=)
c.*28+1759T= (p.=)
c.2050-35T= (p.=)
c.2026-35T= (p.=)
c.1384-35T= (p.=)
7g.55174688G>ACA1101518205EGFRc.2185-34G>A (p.=)
c.*28+1760G>A (p.=)
c.2050-34G>A (p.=)
c.2026-34G>A (p.=)
c.1384-34G>A (p.=)
7g.55174688G=CA1708918261EGFRc.2185-34G= (p.=)
c.*28+1760G= (p.=)
c.2050-34G= (p.=)
c.2026-34G= (p.=)
c.1384-34G= (p.=)
7g.55174692G>ACA4266003EGFRc.2185-30G>A (p.=)
c.*28+1764G>A (p.=)
c.2050-30G>A (p.=)
c.2026-30G>A (p.=)
c.1384-30G>A (p.=)
dbSNP ExAC gnomAD
7g.55174692G=CA1708918262EGFRc.2185-30G= (p.=)
c.*28+1764G= (p.=)
c.2050-30G= (p.=)
c.2026-30G= (p.=)
c.1384-30G= (p.=)
7g.55174697C>ACA574335564EGFRc.2185-25C>A (p.=)
c.*28+1769C>A (p.=)
c.2050-25C>A (p.=)
c.2026-25C>A (p.=)
c.1384-25C>A (p.=)
gnomAD
7g.55174697C=CA1708918263EGFRc.2185-25C= (p.=)
c.*28+1769C= (p.=)
c.2050-25C= (p.=)
c.2026-25C= (p.=)
c.1384-25C= (p.=)
7g.55174697C>TCA574335562EGFRc.2185-25C>T (p.=)
c.*28+1769C>T (p.=)
c.2050-25C>T (p.=)
c.2026-25C>T (p.=)
c.1384-25C>T (p.=)
gnomAD
7g.55174698G>ACA4266004EGFRc.2185-24G>A (p.=)
c.*28+1770G>A (p.=)
c.2050-24G>A (p.=)
c.2026-24G>A (p.=)
c.1384-24G>A (p.=)
dbSNP ExAC gnomAD
7g.55174698G>CCA839813234EGFRc.2185-24G>C (p.=)
c.*28+1770G>C (p.=)
c.2050-24G>C (p.=)
c.2026-24G>C (p.=)
c.1384-24G>C (p.=)
7g.55174698G=CA1708918264EGFRc.2185-24G= (p.=)
c.*28+1770G= (p.=)
c.2050-24G= (p.=)
c.2026-24G= (p.=)
c.1384-24G= (p.=)
7g.55174700C=CA1708918265EGFRc.2185-22C= (p.=)
c.*28+1772C= (p.=)
c.2050-22C= (p.=)
c.2026-22C= (p.=)
c.1384-22C= (p.=)
7g.55174700C>GCA4266005EGFRc.2185-22C>G (p.=)
c.*28+1772C>G (p.=)
c.2050-22C>G (p.=)
c.2026-22C>G (p.=)
c.1384-22C>G (p.=)
dbSNP ExAC gnomAD
7g.55174702T>CCA839813247EGFRc.2185-20T>C (p.=)
c.*28+1774T>C (p.=)
c.2050-20T>C (p.=)
c.2026-20T>C (p.=)
c.1384-20T>C (p.=)
7g.55174702T=CA1708918266EGFRc.2185-20T= (p.=)
c.*28+1774T= (p.=)
c.2050-20T= (p.=)
c.2026-20T= (p.=)
c.1384-20T= (p.=)
7g.55174704C=CA1708918267EGFRc.2185-18C= (p.=)
c.*28+1776C= (p.=)
c.2050-18C= (p.=)
c.2026-18C= (p.=)
c.1384-18C= (p.=)
7g.55174704C>TCA4266006EGFRc.2185-18C>T (p.=)
c.*28+1776C>T (p.=)
c.2050-18C>T (p.=)
c.2026-18C>T (p.=)
c.1384-18C>T (p.=)
dbSNP ExAC gnomAD
7g.55174705_55174707delinsTTCCA1708918268EGFRc.2185-17_2185-15delinsTTC (p.=)
c.*28+1777_*28+1779delinsTTC (p.=)
c.2050-17_2050-15delinsTTC (p.=)
c.2026-17_2026-15delinsTTC (p.=)
c.1384-17_1384-15delinsTTC (p.=)
7g.55174713_55174714delCA1708918269EGFRc.2185-9_2185-8del (p.=)
c.*28+1785_*28+1786del (p.=)
c.2050-9_2050-8del (p.=)
c.2026-9_2026-8del (p.=)
c.1384-9_1384-8del (p.=)
dbSNP
7g.55174709C=CA1708918270EGFRc.2185-13C= (p.=)
c.*28+1781C= (p.=)
c.2050-13C= (p.=)
c.2026-13C= (p.=)
c.1384-13C= (p.=)
7g.55174709C>TCA4266007EGFRc.2185-13C>T (p.=)
c.*28+1781C>T (p.=)
c.2050-13C>T (p.=)
c.2026-13C>T (p.=)
c.1384-13C>T (p.=)
dbSNP ExAC gnomAD
7g.55174710T>ACA1101518211EGFRc.2185-12T>A (p.=)
c.*28+1782T>A (p.=)
c.2050-12T>A (p.=)
c.2026-12T>A (p.=)
c.1384-12T>A (p.=)
7g.55174710T=CA1708918271EGFRc.2185-12T= (p.=)
c.*28+1782T= (p.=)
c.2050-12T= (p.=)
c.2026-12T= (p.=)
c.1384-12T= (p.=)
7g.55174711C=CA1708918272EGFRc.2185-11C= (p.=)
c.*28+1783C= (p.=)
c.2050-11C= (p.=)
c.2026-11C= (p.=)
c.1384-11C= (p.=)
7g.55174711C>GCA839813258EGFRc.2185-11C>G (p.=)
c.*28+1783C>G (p.=)
c.2050-11C>G (p.=)
c.2026-11C>G (p.=)
c.1384-11C>G (p.=)
7g.55174713C=CA1708918273EGFRc.2185-9C= (p.=)
c.*28+1785C= (p.=)
c.2050-9C= (p.=)
c.2026-9C= (p.=)
c.1384-9C= (p.=)
7g.55174713C>GCA1708918274EGFRc.2185-9C>G (p.=)
c.*28+1785C>G (p.=)
c.2050-9C>G (p.=)
c.2026-9C>G (p.=)
c.1384-9C>G (p.=)
7g.55174715G>CCA1708918276EGFRc.2185-7G>C (p.=)
c.*28+1787G>C (p.=)
c.2050-7G>C (p.=)
c.2026-7G>C (p.=)
c.1384-7G>C (p.=)
7g.55174715G=CA1708918275EGFRc.2185-7G= (p.=)
c.*28+1787G= (p.=)
c.2050-7G= (p.=)
c.2026-7G= (p.=)
c.1384-7G= (p.=)
7g.55174717C=CA1708918277EGFRc.2185-5C= (p.=)
c.*28+1789C= (p.=)
c.2050-5C= (p.=)
c.2026-5C= (p.=)
c.1384-5C= (p.=)
7g.55174717C>TCA4266008EGFRc.2185-5C>T (p.=)
c.*28+1789C>T (p.=)
c.2050-5C>T (p.=)
c.2026-5C>T (p.=)
c.1384-5C>T (p.=)
ClinVar dbSNP ExAC gnomAD
7g.55174718A=CA1708918278EGFRc.2185-4A= (p.=)
c.*28+1790A= (p.=)
c.2050-4A= (p.=)
c.2026-4A= (p.=)
c.1384-4A= (p.=)
7g.55174718A>GCA158932430EGFRc.2185-4A>G (p.=)
c.*28+1790A>G (p.=)
c.2050-4A>G (p.=)
c.2026-4A>G (p.=)
c.1384-4A>G (p.=)
dbSNP

Number of alleles fetched