Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.109980963C>A | CA357885156 | EGF | c.2359C>A (p.Gln787Lys) c.2233C>A (p.Gln745Lys) n.287C>A n.323C>A c.2248C>A (p.Gln750Lys) n.2812C>A c.2383C>A (p.Gln795Lys) c.2257C>A (p.Gln753Lys) n.2836C>A | |
4 | g.109980963C>G | CA357885157 | EGF | c.2359C>G (p.Gln787Glu) c.2233C>G (p.Gln745Glu) n.287C>G n.323C>G c.2248C>G (p.Gln750Glu) n.2812C>G c.2383C>G (p.Gln795Glu) c.2257C>G (p.Gln753Glu) n.2836C>G | |
4 | g.109980963C>T | CA357885158 | EGF | c.2359C>T (p.Gln787Ter) c.2233C>T (p.Gln745Ter) n.287C>T n.323C>T c.2248C>T (p.Gln750Ter) n.2812C>T c.2383C>T (p.Gln795Ter) c.2257C>T (p.Gln753Ter) n.2836C>T | |
4 | g.109980964A= | CA1484811176 | EGF | c.2360A= (p.Gln787=) c.2234A= (p.Gln745=) n.288A= n.324A= c.2249A= (p.Gln750=) n.2813A= c.2384A= (p.Gln795=) c.2258A= (p.Gln753=) n.2837A= | |
4 | g.109980964A>C | CA357885159 | EGF | c.2360A>C (p.Gln787Pro) c.2234A>C (p.Gln745Pro) n.288A>C n.324A>C c.2249A>C (p.Gln750Pro) n.2813A>C c.2384A>C (p.Gln795Pro) c.2258A>C (p.Gln753Pro) n.2837A>C | |
4 | g.109980964A>G | CA357885160 | EGF | c.2360A>G (p.Gln787Arg) c.2234A>G (p.Gln745Arg) n.288A>G n.324A>G c.2249A>G (p.Gln750Arg) n.2813A>G c.2384A>G (p.Gln795Arg) c.2258A>G (p.Gln753Arg) n.2837A>G | dbSNP |
4 | g.109980964A>T | CA357885161 | EGF | c.2360A>T (p.Gln787Leu) c.2234A>T (p.Gln745Leu) n.288A>T n.324A>T c.2249A>T (p.Gln750Leu) n.2813A>T c.2384A>T (p.Gln795Leu) c.2258A>T (p.Gln753Leu) n.2837A>T | |
4 | g.109980965G>A | CA440594106 | EGF | c.2361G>A (p.Gln787=) c.2235G>A (p.Gln745=) n.289G>A n.325G>A c.2250G>A (p.Gln750=) n.2814G>A c.2385G>A (p.Gln795=) c.2259G>A (p.Gln753=) n.2838G>A | |
4 | g.109980965G>C | CA3043941 | EGF | c.2361G>C (p.Gln787His) c.2235G>C (p.Gln745His) n.289G>C n.325G>C c.2250G>C (p.Gln750His) n.2814G>C c.2385G>C (p.Gln795His) c.2259G>C (p.Gln753His) n.2838G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.109980965G= | CA1484811179 | EGF | c.2361G= (p.Gln787=) c.2235G= (p.Gln745=) n.289G= n.325G= c.2250G= (p.Gln750=) n.2814G= c.2385G= (p.Gln795=) c.2259G= (p.Gln753=) n.2838G= | |
4 | g.109980965G>T | CA357885162 | EGF | c.2361G>T (p.Gln787His) c.2235G>T (p.Gln745His) n.289G>T n.325G>T c.2250G>T (p.Gln750His) n.2814G>T c.2385G>T (p.Gln795His) c.2259G>T (p.Gln753His) n.2838G>T | |
4 | g.109980966C>A | CA357885163 | EGF | c.2362C>A (p.Leu788Met) c.2236C>A (p.Leu746Met) n.290C>A n.326C>A c.2251C>A (p.Leu751Met) n.2815C>A c.2386C>A (p.Leu796Met) c.2260C>A (p.Leu754Met) n.2839C>A | |
4 | g.109980966C= | CA1484811189 | EGF | c.2362C= (p.Leu788=) c.2236C= (p.Leu746=) n.290C= n.326C= c.2251C= (p.Leu751=) n.2815C= c.2386C= (p.Leu796=) c.2260C= (p.Leu754=) n.2839C= | |
4 | g.109980966C>G | CA357885164 | EGF | c.2362C>G (p.Leu788Val) c.2236C>G (p.Leu746Val) n.290C>G n.326C>G c.2251C>G (p.Leu751Val) n.2815C>G c.2386C>G (p.Leu796Val) c.2260C>G (p.Leu754Val) n.2839C>G | |
4 | g.109980966C>T | CA3043942 | EGF | c.2362C>T (p.Leu788=) c.2236C>T (p.Leu746=) n.290C>T n.326C>T c.2251C>T (p.Leu751=) n.2815C>T c.2386C>T (p.Leu796=) c.2260C>T (p.Leu754=) n.2839C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.109980967T>A | CA357885165 | EGF | c.2363T>A (p.Leu788Gln) c.2237T>A (p.Leu746Gln) n.291T>A n.327T>A c.2252T>A (p.Leu751Gln) n.2816T>A c.2387T>A (p.Leu796Gln) c.2261T>A (p.Leu754Gln) n.2840T>A | |
4 | g.109980967T>C | CA357885167 | EGF | c.2363T>C (p.Leu788Pro) c.2237T>C (p.Leu746Pro) n.291T>C n.327T>C c.2252T>C (p.Leu751Pro) n.2816T>C c.2387T>C (p.Leu796Pro) c.2261T>C (p.Leu754Pro) n.2840T>C | |
4 | g.109980967T>G | CA357885166 | EGF | c.2363T>G (p.Leu788Arg) c.2237T>G (p.Leu746Arg) n.291T>G n.327T>G c.2252T>G (p.Leu751Arg) n.2816T>G c.2387T>G (p.Leu796Arg) c.2261T>G (p.Leu754Arg) n.2840T>G | |
4 | g.109980968G>A | CA440594111 | EGF | c.2364G>A (p.Leu788=) c.2238G>A (p.Leu746=) n.292G>A n.328G>A c.2253G>A (p.Leu751=) n.2817G>A c.2388G>A (p.Leu796=) c.2262G>A (p.Leu754=) n.2841G>A | gnomAD v4 COSMIC |
4 | g.109980968G>C | CA440594112 | EGF | c.2364G>C (p.Leu788=) c.2238G>C (p.Leu746=) n.292G>C n.328G>C c.2253G>C (p.Leu751=) n.2817G>C c.2388G>C (p.Leu796=) c.2262G>C (p.Leu754=) n.2841G>C | |
4 | g.109980968G= | CA1484811198 | EGF | c.2364G= (p.Leu788=) c.2238G= (p.Leu746=) n.292G= n.328G= c.2253G= (p.Leu751=) n.2817G= c.2388G= (p.Leu796=) c.2262G= (p.Leu754=) n.2841G= | |
4 | g.109980968G>T | CA3043943 | EGF | c.2364G>T (p.Leu788=) c.2238G>T (p.Leu746=) n.292G>T n.328G>T c.2253G>T (p.Leu751=) n.2817G>T c.2388G>T (p.Leu796=) c.2262G>T (p.Leu754=) n.2841G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.109980969T>A | CA357885169 | EGF | c.2365T>A (p.Leu789Met) c.2239T>A (p.Leu747Met) n.293T>A n.329T>A c.2254T>A (p.Leu752Met) n.2818T>A c.2389T>A (p.Leu797Met) c.2263T>A (p.Leu755Met) n.2842T>A | gnomAD v4 |
4 | g.109980969T>C | CA3043944 | EGF | c.2365T>C (p.Leu789=) c.2239T>C (p.Leu747=) n.293T>C n.329T>C c.2254T>C (p.Leu752=) n.2818T>C c.2389T>C (p.Leu797=) c.2263T>C (p.Leu755=) n.2842T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.109980969T>G | CA357885168 | EGF | c.2365T>G (p.Leu789Val) c.2239T>G (p.Leu747Val) n.293T>G n.329T>G c.2254T>G (p.Leu752Val) n.2818T>G c.2389T>G (p.Leu797Val) c.2263T>G (p.Leu755Val) n.2842T>G | |
4 | g.109980969T= | CA1484811204 | EGF | c.2365T= (p.Leu789=) c.2239T= (p.Leu747=) n.293T= n.329T= c.2254T= (p.Leu752=) n.2818T= c.2389T= (p.Leu797=) c.2263T= (p.Leu755=) n.2842T= | |
4 | g.109980970T>A | CA357885170 | EGF | c.2366T>A (p.Leu789Ter) c.2240T>A (p.Leu747Ter) n.294T>A n.330T>A c.2255T>A (p.Leu752Ter) n.2819T>A c.2390T>A (p.Leu797Ter) c.2264T>A (p.Leu755Ter) n.2843T>A | gnomAD v4 |
4 | g.109980970T>C | CA357885171 | EGF | c.2366T>C (p.Leu789Ser) c.2240T>C (p.Leu747Ser) n.294T>C n.330T>C c.2255T>C (p.Leu752Ser) n.2819T>C c.2390T>C (p.Leu797Ser) c.2264T>C (p.Leu755Ser) n.2843T>C | |
4 | g.109980970T>G | CA357885172 | EGF | c.2366T>G (p.Leu789Trp) c.2240T>G (p.Leu747Trp) n.294T>G n.330T>G c.2255T>G (p.Leu752Trp) n.2819T>G c.2390T>G (p.Leu797Trp) c.2264T>G (p.Leu755Trp) n.2843T>G | |
4 | g.109980971G>A | CA440594113 | EGF | c.2367G>A (p.Leu789=) c.2241G>A (p.Leu747=) n.295G>A n.331G>A c.2256G>A (p.Leu752=) n.2820G>A c.2391G>A (p.Leu797=) c.2265G>A (p.Leu755=) n.2844G>A | |
4 | g.109980971G>C | CA357885173 | EGF | c.2367G>C (p.Leu789Phe) c.2241G>C (p.Leu747Phe) n.295G>C n.331G>C c.2256G>C (p.Leu752Phe) n.2820G>C c.2391G>C (p.Leu797Phe) c.2265G>C (p.Leu755Phe) n.2844G>C | |
4 | g.109980971G>T | CA357885174 | EGF | c.2367G>T (p.Leu789Phe) c.2241G>T (p.Leu747Phe) n.295G>T n.331G>T c.2256G>T (p.Leu752Phe) n.2820G>T c.2391G>T (p.Leu797Phe) c.2265G>T (p.Leu755Phe) n.2844G>T | gnomAD v4 |
4 | g.109980972G>A | CA357885175 | EGF | c.2368G>A (p.Ala790Thr) c.2242G>A (p.Ala748Thr) n.296G>A n.332G>A c.2257G>A (p.Ala753Thr) n.2821G>A c.2392G>A (p.Ala798Thr) c.2266G>A (p.Ala756Thr) n.2845G>A | dbSNP |
4 | g.109980972G>C | CA357885176 | EGF | c.2368G>C (p.Ala790Pro) c.2242G>C (p.Ala748Pro) n.296G>C n.332G>C c.2257G>C (p.Ala753Pro) n.2821G>C c.2392G>C (p.Ala798Pro) c.2266G>C (p.Ala756Pro) n.2845G>C | |
4 | g.109980972G= | CA1484811207 | EGF | c.2368G= (p.Ala790=) c.2242G= (p.Ala748=) n.296G= n.332G= c.2257G= (p.Ala753=) n.2821G= c.2392G= (p.Ala798=) c.2266G= (p.Ala756=) n.2845G= | |
4 | g.109980972G>T | CA357885177 | EGF | c.2368G>T (p.Ala790Ser) c.2242G>T (p.Ala748Ser) n.296G>T n.332G>T c.2257G>T (p.Ala753Ser) n.2821G>T c.2392G>T (p.Ala798Ser) c.2266G>T (p.Ala756Ser) n.2845G>T | dbSNP |
4 | g.109980973C>A | CA3043945 | EGF | c.2369C>A (p.Ala790Glu) c.2243C>A (p.Ala748Glu) n.297C>A n.333C>A c.2258C>A (p.Ala753Glu) n.2822C>A c.2393C>A (p.Ala798Glu) c.2267C>A (p.Ala756Glu) n.2846C>A | dbSNP ExAC gnomAD v2 |
4 | g.109980973C= | CA1484811212 | EGF | c.2369C= (p.Ala790=) c.2243C= (p.Ala748=) n.297C= n.333C= c.2258C= (p.Ala753=) n.2822C= c.2393C= (p.Ala798=) c.2267C= (p.Ala756=) n.2846C= | |
4 | g.109980973C>G | CA357885178 | EGF | c.2369C>G (p.Ala790Gly) c.2243C>G (p.Ala748Gly) n.297C>G n.333C>G c.2258C>G (p.Ala753Gly) n.2822C>G c.2393C>G (p.Ala798Gly) c.2267C>G (p.Ala756Gly) n.2846C>G | |
4 | g.109980973C>T | CA357885179 | EGF | c.2369C>T (p.Ala790Val) c.2243C>T (p.Ala748Val) n.297C>T n.333C>T c.2258C>T (p.Ala753Val) n.2822C>T c.2393C>T (p.Ala798Val) c.2267C>T (p.Ala756Val) n.2846C>T | dbSNP |
4 | g.109980974A>C | CA440594115 | EGF | c.2370A>C (p.Ala790=) c.2244A>C (p.Ala748=) n.298A>C n.334A>C c.2259A>C (p.Ala753=) n.2823A>C c.2394A>C (p.Ala798=) c.2268A>C (p.Ala756=) n.2847A>C | |
4 | g.109980974A>G | CA440594116 | EGF | c.2370A>G (p.Ala790=) c.2244A>G (p.Ala748=) n.298A>G n.334A>G c.2259A>G (p.Ala753=) n.2823A>G c.2394A>G (p.Ala798=) c.2268A>G (p.Ala756=) n.2847A>G | |
4 | g.109980974A>T | CA440594117 | EGF | c.2370A>T (p.Ala790=) c.2244A>T (p.Ala748=) n.298A>T n.334A>T c.2259A>T (p.Ala753=) n.2823A>T c.2394A>T (p.Ala798=) c.2268A>T (p.Ala756=) n.2847A>T | |
4 | g.109980975G>A | CA3043946 | EGF | c.2371G>A (p.Gly791Ser) c.2245G>A (p.Gly749Ser) n.299G>A n.335G>A c.2260G>A (p.Gly754Ser) n.2824G>A c.2395G>A (p.Gly799Ser) c.2269G>A (p.Gly757Ser) n.2848G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.109980975G>C | CA357885181 | EGF | c.2371G>C (p.Gly791Arg) c.2245G>C (p.Gly749Arg) n.299G>C n.335G>C c.2260G>C (p.Gly754Arg) n.2824G>C c.2395G>C (p.Gly799Arg) c.2269G>C (p.Gly757Arg) n.2848G>C | |
4 | g.109980975G= | CA1484811222 | EGF | c.2371G= (p.Gly791=) c.2245G= (p.Gly749=) n.299G= n.335G= c.2260G= (p.Gly754=) n.2824G= c.2395G= (p.Gly799=) c.2269G= (p.Gly757=) n.2848G= | |
4 | g.109980975G>T | CA357885180 | EGF | c.2371G>T (p.Gly791Cys) c.2245G>T (p.Gly749Cys) n.299G>T n.335G>T c.2260G>T (p.Gly754Cys) n.2824G>T c.2395G>T (p.Gly799Cys) c.2269G>T (p.Gly757Cys) n.2848G>T | |
4 | g.109980976G>A | CA3043947 | EGF | c.2371+1G>A (n.2371+1G>A) c.2245+1G>A (n.2245+1G>A) n.299+1G>A n.335+1G>A c.2260+1G>A (n.2260+1G>A) n.2824+1G>A c.2395+1G>A (n.2395+1G>A) c.2269+1G>A (n.2269+1G>A) n.2848+1G>A | dbSNP ExAC gnomAD v2 |
4 | g.109980976G>C | CA357885182 | EGF | c.2371+1G>C (n.2371+1G>C) c.2245+1G>C (n.2245+1G>C) n.299+1G>C n.335+1G>C c.2260+1G>C (n.2260+1G>C) n.2824+1G>C c.2395+1G>C (n.2395+1G>C) c.2269+1G>C (n.2269+1G>C) n.2848+1G>C | |
4 | g.109980976G= | CA1484811231 | EGF | c.2371+1G= (n.2371+1G=) c.2245+1G= (n.2245+1G=) n.299+1G= n.335+1G= c.2260+1G= (n.2260+1G=) n.2824+1G= c.2395+1G= (n.2395+1G=) c.2269+1G= (n.2269+1G=) n.2848+1G= |