Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.29197588T>A | CA346466020 | ALK,CLIP4 | c.*582T>A (n.*582T>A) c.4027A>T (p.Thr1343Ser) c.1254A>T n.904A>T c.823A>T (p.Thr275Ser) c.907A>T (p.Thr303Ser) c.2896A>T (p.Thr966Ser) c.1180A>T (p.Thr394Ser) | dbSNP |
2 | g.29197588T>C | CA346466022 | ALK,CLIP4 | c.*582T>C (n.*582T>C) c.4027A>G (p.Thr1343Ala) c.1254A>G n.904A>G c.823A>G (p.Thr275Ala) c.907A>G (p.Thr303Ala) c.2896A>G (p.Thr966Ala) c.1180A>G (p.Thr394Ala) | dbSNP |
2 | g.29197588T>G | CA346466025 | ALK,CLIP4 | c.*582T>G (n.*582T>G) c.4027A>C (p.Thr1343Pro) c.1254A>C n.904A>C c.823A>C (p.Thr275Pro) c.907A>C (p.Thr303Pro) c.2896A>C (p.Thr966Pro) c.1180A>C (p.Thr394Pro) | dbSNP |
2 | g.29197589G>A | CA425433905 | ALK,CLIP4 | c.*583G>A (n.*583G>A) c.4026C>T (p.Val1342=) c.1253C>T n.903C>T c.822C>T (p.Val274=) c.906C>T (p.Val302=) c.2895C>T (p.Val965=) c.1179C>T (p.Val393=) | ClinVar dbSNP |
2 | g.29197589G>C | CA425433906 | ALK,CLIP4 | c.*583G>C (n.*583G>C) c.4026C>G (p.Val1342=) c.1253C>G n.903C>G c.822C>G (p.Val274=) c.906C>G (p.Val302=) c.2895C>G (p.Val965=) c.1179C>G (p.Val393=) | dbSNP |
2 | g.29197589G>T | CA425433907 | ALK,CLIP4 | c.*583G>T (n.*583G>T) c.4026C>A (p.Val1342=) c.1253C>A n.903C>A c.822C>A (p.Val274=) c.906C>A (p.Val302=) c.2895C>A (p.Val965=) c.1179C>A (p.Val393=) | |
2 | g.29197590A>C | CA346466027 | ALK,CLIP4 | c.*584A>C (n.*584A>C) c.4025T>G (p.Val1342Gly) c.1252T>G n.902T>G c.821T>G (p.Val274Gly) c.905T>G (p.Val302Gly) c.2894T>G (p.Val965Gly) c.1178T>G (p.Val393Gly) | dbSNP |
2 | g.29197590A>G | CA346466030 | ALK,CLIP4 | c.*584A>G (n.*584A>G) c.4025T>C (p.Val1342Ala) c.1252T>C n.902T>C c.821T>C (p.Val274Ala) c.905T>C (p.Val302Ala) c.2894T>C (p.Val965Ala) c.1178T>C (p.Val393Ala) | dbSNP |
2 | g.29197590A>T | CA346466032 | ALK,CLIP4 | c.*584A>T (n.*584A>T) c.4025T>A (p.Val1342Asp) c.1252T>A n.902T>A c.821T>A (p.Val274Asp) c.905T>A (p.Val302Asp) c.2894T>A (p.Val965Asp) c.1178T>A (p.Val393Asp) | ClinVar dbSNP |
2 | g.29197591C>A | CA346466038 | ALK,CLIP4 | c.*585C>A (n.*585C>A) c.4024G>T (p.Val1342Phe) c.1251G>T n.901G>T c.820G>T (p.Val274Phe) c.904G>T (p.Val302Phe) c.2893G>T (p.Val965Phe) c.1177G>T (p.Val393Phe) | |
2 | g.29197591C= | CA1241075333 | ALK,CLIP4 | c.*585C= (n.*585C=) c.4024G= (p.Val1342=) c.1251G= n.901G= c.820G= (p.Val274=) c.904G= (p.Val302=) c.2893G= (p.Val965=) c.1177G= (p.Val393=) | |
2 | g.29197591C>G | CA346466036 | ALK,CLIP4 | c.*585C>G (n.*585C>G) c.4024G>C (p.Val1342Leu) c.1251G>C n.901G>C c.820G>C (p.Val274Leu) c.904G>C (p.Val302Leu) c.2893G>C (p.Val965Leu) c.1177G>C (p.Val393Leu) | |
2 | g.29197591C>T | CA1593703 | ALK,CLIP4 | c.*585C>T (n.*585C>T) c.4024G>A (p.Val1342Ile) c.1251G>A n.901G>A c.820G>A (p.Val274Ile) c.904G>A (p.Val302Ile) c.2893G>A (p.Val965Ile) c.1177G>A (p.Val393Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29197592A>C | CA346466040 | ALK,CLIP4 | c.*586A>C (n.*586A>C) c.4023T>G (p.Phe1341Leu) c.1250T>G n.900T>G c.819T>G (p.Phe273Leu) c.903T>G (p.Phe301Leu) c.2892T>G (p.Phe964Leu) c.1176T>G (p.Phe392Leu) | |
2 | g.29197592A>G | CA425433908 | ALK,CLIP4 | c.*586A>G (n.*586A>G) c.4023T>C (p.Phe1341=) c.1250T>C n.900T>C c.819T>C (p.Phe273=) c.903T>C (p.Phe301=) c.2892T>C (p.Phe964=) c.1176T>C (p.Phe392=) | ClinVar |
2 | g.29197592A>T | CA346466043 | ALK,CLIP4 | c.*586A>T (n.*586A>T) c.4023T>A (p.Phe1341Leu) c.1250T>A n.900T>A c.819T>A (p.Phe273Leu) c.903T>A (p.Phe301Leu) c.2892T>A (p.Phe964Leu) c.1176T>A (p.Phe392Leu) | dbSNP |
2 | g.29197593_29197594del | CA2580066451 | ALK,CLIP4 | c.*587_*588del (n.*587_*588del) c.4022_4023del (p.Phe1341CysfsTer30) c.1249_1250del n.899_900del c.818_819del (p.Phe273CysfsTer30) c.902_903del (p.Phe301CysfsTer30) c.2891_2892del (p.Phe964CysfsTer30) c.1175_1176del (p.Phe392CysfsTer30) | ClinVar |
2 | g.29197593A>C | CA346466045 | ALK,CLIP4 | c.*587A>C (n.*587A>C) c.4022T>G (p.Phe1341Cys) c.1249T>G n.899T>G c.818T>G (p.Phe273Cys) c.902T>G (p.Phe301Cys) c.2891T>G (p.Phe964Cys) c.1175T>G (p.Phe392Cys) | |
2 | g.29197593A>G | CA346466047 | ALK,CLIP4 | c.*587A>G (n.*587A>G) c.4022T>C (p.Phe1341Ser) c.1249T>C n.899T>C c.818T>C (p.Phe273Ser) c.902T>C (p.Phe301Ser) c.2891T>C (p.Phe964Ser) c.1175T>C (p.Phe392Ser) | dbSNP COSMIC |
2 | g.29197593A>T | CA346466048 | ALK,CLIP4 | c.*587A>T (n.*587A>T) c.4022T>A (p.Phe1341Tyr) c.1249T>A n.899T>A c.818T>A (p.Phe273Tyr) c.902T>A (p.Phe301Tyr) c.2891T>A (p.Phe964Tyr) c.1175T>A (p.Phe392Tyr) | dbSNP |
2 | g.29197594A>C | CA346466051 | ALK,CLIP4 | c.*588A>C (n.*588A>C) c.4021T>G (p.Phe1341Val) c.1248T>G n.898T>G c.817T>G (p.Phe273Val) c.901T>G (p.Phe301Val) c.2890T>G (p.Phe964Val) c.1174T>G (p.Phe392Val) | dbSNP |
2 | g.29197594A>G | CA346466053 | ALK,CLIP4 | c.*588A>G (n.*588A>G) c.4021T>C (p.Phe1341Leu) c.1248T>C n.898T>C c.817T>C (p.Phe273Leu) c.901T>C (p.Phe301Leu) c.2890T>C (p.Phe964Leu) c.1174T>C (p.Phe392Leu) | dbSNP |
2 | g.29197594A>T | CA346466054 | ALK,CLIP4 | c.*588A>T (n.*588A>T) c.4021T>A (p.Phe1341Ile) c.1248T>A n.898T>A c.817T>A (p.Phe273Ile) c.901T>A (p.Phe301Ile) c.2890T>A (p.Phe964Ile) c.1174T>A (p.Phe392Ile) | dbSNP |
2 | g.29197595C>A | CA346466055 | ALK,CLIP4 | c.*589C>A (n.*589C>A) c.4020G>T (p.Glu1340Asp) c.1247G>T n.897G>T c.816G>T (p.Glu272Asp) c.900G>T (p.Glu300Asp) c.2889G>T (p.Glu963Asp) c.1173G>T (p.Glu391Asp) | dbSNP |
2 | g.29197595C>G | CA346466056 | ALK,CLIP4 | c.*589C>G (n.*589C>G) c.4020G>C (p.Glu1340Asp) c.1247G>C n.897G>C c.816G>C (p.Glu272Asp) c.900G>C (p.Glu300Asp) c.2889G>C (p.Glu963Asp) c.1173G>C (p.Glu391Asp) | dbSNP |
2 | g.29197595C>T | CA425433909 | ALK,CLIP4 | c.*589C>T (n.*589C>T) c.4020G>A (p.Glu1340=) c.1247G>A n.897G>A c.816G>A (p.Glu272=) c.900G>A (p.Glu300=) c.2889G>A (p.Glu963=) c.1173G>A (p.Glu391=) | ClinVar dbSNP |
2 | g.29197596T>A | CA346466059 | ALK,CLIP4 | c.*590T>A (n.*590T>A) c.4019A>T (p.Glu1340Val) c.1246A>T n.896A>T c.815A>T (p.Glu272Val) c.899A>T (p.Glu300Val) c.2888A>T (p.Glu963Val) c.1172A>T (p.Glu391Val) | COSMIC |
2 | g.29197596T>C | CA346466061 | ALK,CLIP4 | c.*590T>C (n.*590T>C) c.4019A>G (p.Glu1340Gly) c.1246A>G n.896A>G c.815A>G (p.Glu272Gly) c.899A>G (p.Glu300Gly) c.2888A>G (p.Glu963Gly) c.1172A>G (p.Glu391Gly) | ClinVar dbSNP gnomAD v4 |
2 | g.29197596T>G | CA346466063 | ALK,CLIP4 | c.*590T>G (n.*590T>G) c.4019A>C (p.Glu1340Ala) c.1246A>C n.896A>C c.815A>C (p.Glu272Ala) c.899A>C (p.Glu300Ala) c.2888A>C (p.Glu963Ala) c.1172A>C (p.Glu391Ala) | |
2 | g.29197596T= | CA1241075335 | ALK,CLIP4 | c.*590T= (n.*590T=) c.4019A= (p.Glu1340=) c.1246A= n.896A= c.815A= (p.Glu272=) c.899A= (p.Glu300=) c.2888A= (p.Glu963=) c.1172A= (p.Glu391=) | |
2 | g.29197597C>A | CA346466067 | ALK,CLIP4 | c.*591C>A (n.*591C>A) c.4018G>T (p.Glu1340Ter) c.1245G>T n.895G>T c.814G>T (p.Glu272Ter) c.898G>T (p.Glu300Ter) c.2887G>T (p.Glu963Ter) c.1171G>T (p.Glu391Ter) | |
2 | g.29197597C>G | CA346466070 | ALK,CLIP4 | c.*591C>G (n.*591C>G) c.4018G>C (p.Glu1340Gln) c.1245G>C n.895G>C c.814G>C (p.Glu272Gln) c.898G>C (p.Glu300Gln) c.2887G>C (p.Glu963Gln) c.1171G>C (p.Glu391Gln) | |
2 | g.29197597C>T | CA346466065 | ALK,CLIP4 | c.*591C>T (n.*591C>T) c.4018G>A (p.Glu1340Lys) c.1245G>A n.895G>A c.814G>A (p.Glu272Lys) c.898G>A (p.Glu300Lys) c.2887G>A (p.Glu963Lys) c.1171G>A (p.Glu391Lys) | |
2 | g.29197598C>A | CA425433910 | ALK,CLIP4 | c.*592C>A (n.*592C>A) c.4017G>T (p.Leu1339=) c.1244G>T n.894G>T c.813G>T (p.Leu271=) c.897G>T (p.Leu299=) c.2886G>T (p.Leu962=) c.1170G>T (p.Leu390=) | dbSNP |
2 | g.29197598C= | CA1241075338 | ALK,CLIP4 | c.*592C= (n.*592C=) c.4017G= (p.Leu1339=) c.1244G= n.894G= c.813G= (p.Leu271=) c.897G= (p.Leu299=) c.2886G= (p.Leu962=) c.1170G= (p.Leu390=) | |
2 | g.29197598C>G | CA425433911 | ALK,CLIP4 | c.*592C>G (n.*592C>G) c.4017G>C (p.Leu1339=) c.1244G>C n.894G>C c.813G>C (p.Leu271=) c.897G>C (p.Leu299=) c.2886G>C (p.Leu962=) c.1170G>C (p.Leu390=) | dbSNP |
2 | g.29197598C>T | CA425433912 | ALK,CLIP4 | c.*592C>T (n.*592C>T) c.4017G>A (p.Leu1339=) c.1244G>A n.894G>A c.813G>A (p.Leu271=) c.897G>A (p.Leu299=) c.2886G>A (p.Leu962=) c.1170G>A (p.Leu390=) | ClinVar dbSNP gnomAD v4 |
2 | g.29197599A= | CA1241075343 | ALK,CLIP4 | c.*593A= (n.*593A=) c.4016T= (p.Leu1339=) c.1243T= n.893T= c.812T= (p.Leu271=) c.896T= (p.Leu299=) c.2885T= (p.Leu962=) c.1169T= (p.Leu390=) | |
2 | g.29197599A>C | CA346466074 | ALK,CLIP4 | c.*593A>C (n.*593A>C) c.4016T>G (p.Leu1339Arg) c.1243T>G n.893T>G c.812T>G (p.Leu271Arg) c.896T>G (p.Leu299Arg) c.2885T>G (p.Leu962Arg) c.1169T>G (p.Leu390Arg) | |
2 | g.29197599A>G | CA1593704 | ALK,CLIP4 | c.*593A>G (n.*593A>G) c.4016T>C (p.Leu1339Pro) c.1243T>C n.893T>C c.812T>C (p.Leu271Pro) c.896T>C (p.Leu299Pro) c.2885T>C (p.Leu962Pro) c.1169T>C (p.Leu390Pro) | dbSNP ExAC gnomAD v2 |
2 | g.29197599A>T | CA346466077 | ALK,CLIP4 | c.*593A>T (n.*593A>T) c.4016T>A (p.Leu1339Gln) c.1243T>A n.893T>A c.812T>A (p.Leu271Gln) c.896T>A (p.Leu299Gln) c.2885T>A (p.Leu962Gln) c.1169T>A (p.Leu390Gln) | dbSNP |
2 | g.29197600G>A | CA425433913 | ALK,CLIP4 | c.*594G>A (n.*594G>A) c.4015C>T (p.Leu1339=) c.1242C>T n.892C>T c.811C>T (p.Leu271=) c.895C>T (p.Leu299=) c.2884C>T (p.Leu962=) c.1168C>T (p.Leu390=) | ClinVar dbSNP |
2 | g.29197600G>C | CA346466081 | ALK,CLIP4 | c.*594G>C (n.*594G>C) c.4015C>G (p.Leu1339Val) c.1242C>G n.892C>G c.811C>G (p.Leu271Val) c.895C>G (p.Leu299Val) c.2884C>G (p.Leu962Val) c.1168C>G (p.Leu390Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197600G= | CA1241075348 | ALK,CLIP4 | c.*594G= (n.*594G=) c.4015C= (p.Leu1339=) c.1242C= n.892C= c.811C= (p.Leu271=) c.895C= (p.Leu299=) c.2884C= (p.Leu962=) c.1168C= (p.Leu390=) | |
2 | g.29197600G>T | CA346466084 | ALK,CLIP4 | c.*594G>T (n.*594G>T) c.4015C>A (p.Leu1339Met) c.1242C>A n.892C>A c.811C>A (p.Leu271Met) c.895C>A (p.Leu299Met) c.2884C>A (p.Leu962Met) c.1168C>A (p.Leu390Met) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.29197600dup | CA767497909 | ALK,CLIP4 | c.*594dup (n.*594dup) c.4015dup (p.Leu1339ProfsTer?) c.1242dup n.892dup c.811dup (p.Leu271ProfsTer?) c.895dup (p.Leu299ProfsTer?) c.2884dup (p.Leu962ProfsTer?) c.1168dup (p.Leu390ProfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197601A>C | CA425433914 | ALK,CLIP4 | c.*595A>C (n.*595A>C) c.4014T>G (p.Val1338=) c.1241T>G n.891T>G c.810T>G (p.Val270=) c.894T>G (p.Val298=) c.2883T>G (p.Val961=) c.1167T>G (p.Val389=) | |
2 | g.29197601A>G | CA425433915 | ALK,CLIP4 | c.*595A>G (n.*595A>G) c.4014T>C (p.Val1338=) c.1241T>C n.891T>C c.810T>C (p.Val270=) c.894T>C (p.Val298=) c.2883T>C (p.Val961=) c.1167T>C (p.Val389=) | |
2 | g.29197601A>T | CA425433916 | ALK,CLIP4 | c.*595A>T (n.*595A>T) c.4014T>A (p.Val1338=) c.1241T>A n.891T>A c.810T>A (p.Val270=) c.894T>A (p.Val298=) c.2883T>A (p.Val961=) c.1167T>A (p.Val389=) | dbSNP |
2 | g.29197602A>C | CA346466087 | ALK,CLIP4 | c.*596A>C (n.*596A>C) c.4013T>G (p.Val1338Gly) c.1240T>G n.890T>G c.809T>G (p.Val270Gly) c.893T>G (p.Val298Gly) c.2882T>G (p.Val961Gly) c.1166T>G (p.Val389Gly) | dbSNP |
2 | g.29197602A>G | CA346466088 | ALK,CLIP4 | c.*596A>G (n.*596A>G) c.4013T>C (p.Val1338Ala) c.1240T>C n.890T>C c.809T>C (p.Val270Ala) c.893T>C (p.Val298Ala) c.2882T>C (p.Val961Ala) c.1166T>C (p.Val389Ala) | |
2 | g.29197602A>T | CA346466091 | ALK,CLIP4 | c.*596A>T (n.*596A>T) c.4013T>A (p.Val1338Asp) c.1240T>A n.890T>A c.809T>A (p.Val270Asp) c.893T>A (p.Val298Asp) c.2882T>A (p.Val961Asp) c.1166T>A (p.Val389Asp) | dbSNP |
2 | g.29197603C>A | CA346466093 | ALK,CLIP4 | c.*597C>A (n.*597C>A) c.4012G>T (p.Val1338Phe) c.1239G>T n.889G>T c.808G>T (p.Val270Phe) c.892G>T (p.Val298Phe) c.2881G>T (p.Val961Phe) c.1165G>T (p.Val389Phe) | ClinVar dbSNP gnomAD v4 |
2 | g.29197603C= | CA1241075355 | ALK,CLIP4 | c.*597C= (n.*597C=) c.4012G= (p.Val1338=) c.1239G= n.889G= c.808G= (p.Val270=) c.892G= (p.Val298=) c.2881G= (p.Val961=) c.1165G= (p.Val389=) | |
2 | g.29197603C>G | CA346466094 | ALK,CLIP4 | c.*597C>G (n.*597C>G) c.4012G>C (p.Val1338Leu) c.1239G>C n.889G>C c.808G>C (p.Val270Leu) c.892G>C (p.Val298Leu) c.2881G>C (p.Val961Leu) c.1165G>C (p.Val389Leu) | dbSNP |
2 | g.29197603C>T | CA346466097 | ALK,CLIP4 | c.*597C>T (n.*597C>T) c.4012G>A (p.Val1338Ile) c.1239G>A n.889G>A c.808G>A (p.Val270Ile) c.892G>A (p.Val298Ile) c.2881G>A (p.Val961Ile) c.1165G>A (p.Val389Ile) | ClinVar dbSNP gnomAD v4 |
2 | g.29197604T>A | CA346466099 | ALK,CLIP4 | c.*598T>A (n.*598T>A) c.4011A>T (p.Glu1337Asp) c.1238A>T n.888A>T c.807A>T (p.Glu269Asp) c.891A>T (p.Glu297Asp) c.2880A>T (p.Glu960Asp) c.1164A>T (p.Glu388Asp) | dbSNP |
2 | g.29197604T>C | CA425433917 | ALK,CLIP4 | c.*598T>C (n.*598T>C) c.4011A>G (p.Glu1337=) c.1238A>G n.888A>G c.807A>G (p.Glu269=) c.891A>G (p.Glu297=) c.2880A>G (p.Glu960=) c.1164A>G (p.Glu388=) | ClinVar dbSNP gnomAD v4 |
2 | g.29197604T>G | CA346466100 | ALK,CLIP4 | c.*598T>G (n.*598T>G) c.4011A>C (p.Glu1337Asp) c.1238A>C n.888A>C c.807A>C (p.Glu269Asp) c.891A>C (p.Glu297Asp) c.2880A>C (p.Glu960Asp) c.1164A>C (p.Glu388Asp) | |
2 | g.29197605T>A | CA346466104 | ALK,CLIP4 | c.*599T>A (n.*599T>A) c.4010A>T (p.Glu1337Val) c.1237A>T n.887A>T c.806A>T (p.Glu269Val) c.890A>T (p.Glu297Val) c.2879A>T (p.Glu960Val) c.1163A>T (p.Glu388Val) | |
2 | g.29197605T>C | CA346466107 | ALK,CLIP4 | c.*599T>C (n.*599T>C) c.4010A>G (p.Glu1337Gly) c.1237A>G n.887A>G c.806A>G (p.Glu269Gly) c.890A>G (p.Glu297Gly) c.2879A>G (p.Glu960Gly) c.1163A>G (p.Glu388Gly) | |
2 | g.29197605T>G | CA346466109 | ALK,CLIP4 | c.*599T>G (n.*599T>G) c.4010A>C (p.Glu1337Ala) c.1237A>C n.887A>C c.806A>C (p.Glu269Ala) c.890A>C (p.Glu297Ala) c.2879A>C (p.Glu960Ala) c.1163A>C (p.Glu388Ala) | |
2 | g.29197606C>A | CA346466115 | ALK,CLIP4 | c.*600C>A (n.*600C>A) c.4009G>T (p.Glu1337Ter) c.1236G>T n.886G>T c.805G>T (p.Glu269Ter) c.889G>T (p.Glu297Ter) c.2878G>T (p.Glu960Ter) c.1162G>T (p.Glu388Ter) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.29197606C= | CA1241075360 | ALK,CLIP4 | c.*600C= (n.*600C=) c.4009G= (p.Glu1337=) c.1236G= n.886G= c.805G= (p.Glu269=) c.889G= (p.Glu297=) c.2878G= (p.Glu960=) c.1162G= (p.Glu388=) | |
2 | g.29197606C>G | CA346466111 | ALK,CLIP4 | c.*600C>G (n.*600C>G) c.4009G>C (p.Glu1337Gln) c.1236G>C n.886G>C c.805G>C (p.Glu269Gln) c.889G>C (p.Glu297Gln) c.2878G>C (p.Glu960Gln) c.1162G>C (p.Glu388Gln) | dbSNP |
2 | g.29197606C>T | CA346466113 | ALK,CLIP4 | c.*600C>T (n.*600C>T) c.4009G>A (p.Glu1337Lys) c.1236G>A n.886G>A c.805G>A (p.Glu269Lys) c.889G>A (p.Glu297Lys) c.2878G>A (p.Glu960Lys) c.1162G>A (p.Glu388Lys) | dbSNP |
2 | g.29197607C>A | CA346466118 | ALK,CLIP4 | c.*601C>A (n.*601C>A) c.4008G>T (p.Gln1336His) c.1235G>T n.885G>T c.804G>T (p.Gln268His) c.888G>T (p.Gln296His) c.2877G>T (p.Gln959His) c.1161G>T (p.Gln387His) | dbSNP COSMIC |
2 | g.29197607C= | CA1241075364 | ALK,CLIP4 | c.*601C= (n.*601C=) c.4008G= (p.Gln1336=) c.1235G= n.885G= c.804G= (p.Gln268=) c.888G= (p.Gln296=) c.2877G= (p.Gln959=) c.1161G= (p.Gln387=) | |
2 | g.29197607C>G | CA1593705 | ALK,CLIP4 | c.*601C>G (n.*601C>G) c.4008G>C (p.Gln1336His) c.1235G>C n.885G>C c.804G>C (p.Gln268His) c.888G>C (p.Gln296His) c.2877G>C (p.Gln959His) c.1161G>C (p.Gln387His) | dbSNP ExAC gnomAD v2 |
2 | g.29197607C>T | CA425433918 | ALK,CLIP4 | c.*601C>T (n.*601C>T) c.4008G>A (p.Gln1336=) c.1235G>A n.885G>A c.804G>A (p.Gln268=) c.888G>A (p.Gln296=) c.2877G>A (p.Gln959=) c.1161G>A (p.Gln387=) | dbSNP |
2 | g.29197608T>A | CA346466121 | ALK,CLIP4 | c.*602T>A (n.*602T>A) c.4007A>T (p.Gln1336Leu) c.1234A>T n.884A>T c.803A>T (p.Gln268Leu) c.887A>T (p.Gln296Leu) c.2876A>T (p.Gln959Leu) c.1160A>T (p.Gln387Leu) | |
2 | g.29197608T>C | CA346466123 | ALK,CLIP4 | c.*602T>C (n.*602T>C) c.4007A>G (p.Gln1336Arg) c.1234A>G n.884A>G c.803A>G (p.Gln268Arg) c.887A>G (p.Gln296Arg) c.2876A>G (p.Gln959Arg) c.1160A>G (p.Gln387Arg) | ClinVar dbSNP gnomAD v4 |
2 | g.29197608T>G | CA346466125 | ALK,CLIP4 | c.*602T>G (n.*602T>G) c.4007A>C (p.Gln1336Pro) c.1234A>C n.884A>C c.803A>C (p.Gln268Pro) c.887A>C (p.Gln296Pro) c.2876A>C (p.Gln959Pro) c.1160A>C (p.Gln387Pro) | |
2 | g.29197608T= | CA1241075368 | ALK,CLIP4 | c.*602T= (n.*602T=) c.4007A= (p.Gln1336=) c.1234A= n.884A= c.803A= (p.Gln268=) c.887A= (p.Gln296=) c.2876A= (p.Gln959=) c.1160A= (p.Gln387=) | |
2 | g.29197609G>A | CA346466127 | ALK,CLIP4 | c.*603G>A (n.*603G>A) c.4006C>T (p.Gln1336Ter) c.1233C>T n.883C>T c.802C>T (p.Gln268Ter) c.886C>T (p.Gln296Ter) c.2875C>T (p.Gln959Ter) c.1159C>T (p.Gln387Ter) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197609G>C | CA346466129 | ALK,CLIP4 | c.*603G>C (n.*603G>C) c.4006C>G (p.Gln1336Glu) c.1233C>G n.883C>G c.802C>G (p.Gln268Glu) c.886C>G (p.Gln296Glu) c.2875C>G (p.Gln959Glu) c.1159C>G (p.Gln387Glu) | |
2 | g.29197609G= | CA1241075372 | ALK,CLIP4 | c.*603G= (n.*603G=) c.4006C= (p.Gln1336=) c.1233C= n.883C= c.802C= (p.Gln268=) c.886C= (p.Gln296=) c.2875C= (p.Gln959=) c.1159C= (p.Gln387=) | |
2 | g.29197609G>T | CA346466131 | ALK,CLIP4 | c.*603G>T (n.*603G>T) c.4006C>A (p.Gln1336Lys) c.1233C>A n.883C>A c.802C>A (p.Gln268Lys) c.886C>A (p.Gln296Lys) c.2875C>A (p.Gln959Lys) c.1159C>A (p.Gln387Lys) | |
2 | g.29197610G>A | CA44638095 | ALK,CLIP4 | c.*604G>A (n.*604G>A) c.4005C>T (p.Asn1335=) c.1232C>T n.882C>T c.801C>T (p.Asn267=) c.885C>T (p.Asn295=) c.2874C>T (p.Asn958=) c.1158C>T (p.Asn386=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197610G>C | CA346466133 | ALK,CLIP4 | c.*604G>C (n.*604G>C) c.4005C>G (p.Asn1335Lys) c.1232C>G n.882C>G c.801C>G (p.Asn267Lys) c.885C>G (p.Asn295Lys) c.2874C>G (p.Asn958Lys) c.1158C>G (p.Asn386Lys) | dbSNP |
2 | g.29197610G= | CA1241075374 | ALK,CLIP4 | c.*604G= (n.*604G=) c.4005C= (p.Asn1335=) c.1232C= n.882C= c.801C= (p.Asn267=) c.885C= (p.Asn295=) c.2874C= (p.Asn958=) c.1158C= (p.Asn386=) | |
2 | g.29197610G>T | CA346466136 | ALK,CLIP4 | c.*604G>T (n.*604G>T) c.4005C>A (p.Asn1335Lys) c.1232C>A n.882C>A c.801C>A (p.Asn267Lys) c.885C>A (p.Asn295Lys) c.2874C>A (p.Asn958Lys) c.1158C>A (p.Asn386Lys) | dbSNP |
2 | g.29197611T>A | CA346466141 | ALK,CLIP4 | c.*605T>A (n.*605T>A) c.4004A>T (p.Asn1335Ile) c.1231A>T n.881A>T c.800A>T (p.Asn267Ile) c.884A>T (p.Asn295Ile) c.2873A>T (p.Asn958Ile) c.1157A>T (p.Asn386Ile) | dbSNP |
2 | g.29197611T>C | CA346466143 | ALK,CLIP4 | c.*605T>C (n.*605T>C) c.4004A>G (p.Asn1335Ser) c.1231A>G n.881A>G c.800A>G (p.Asn267Ser) c.884A>G (p.Asn295Ser) c.2873A>G (p.Asn958Ser) c.1157A>G (p.Asn386Ser) | dbSNP |
2 | g.29197611T>G | CA346466139 | ALK,CLIP4 | c.*605T>G (n.*605T>G) c.4004A>C (p.Asn1335Thr) c.1231A>C n.881A>C c.800A>C (p.Asn267Thr) c.884A>C (p.Asn295Thr) c.2873A>C (p.Asn958Thr) c.1157A>C (p.Asn386Thr) | dbSNP |
2 | g.29197616_29197621dup | CA2658458160 | ALK,CLIP4 | c.*610_*615dup (n.*610_*615dup) c.3999_4004dup (p.Ser1334_Asn1335insLysSer) c.1226_1231dup n.876_881dup c.795_800dup (p.Ser266_Asn267insLysSer) c.879_884dup (p.Ser294_Asn295insLysSer) c.2868_2873dup (p.Ser957_Asn958insLysSer) c.1152_1157dup (p.Ser385_Asn386insLysSer) | gnomAD v4 |
2 | g.29197612T>A | CA346466145 | ALK,CLIP4 | c.*606T>A (n.*606T>A) c.4003A>T (p.Asn1335Tyr) c.1230A>T n.880A>T c.799A>T (p.Asn267Tyr) c.883A>T (p.Asn295Tyr) c.2872A>T (p.Asn958Tyr) c.1156A>T (p.Asn386Tyr) | |
2 | g.29197612T>C | CA346466147 | ALK,CLIP4 | c.*606T>C (n.*606T>C) c.4003A>G (p.Asn1335Asp) c.1230A>G n.880A>G c.799A>G (p.Asn267Asp) c.883A>G (p.Asn295Asp) c.2872A>G (p.Asn958Asp) c.1156A>G (p.Asn386Asp) | |
2 | g.29197612T>G | CA346466151 | ALK,CLIP4 | c.*606T>G (n.*606T>G) c.4003A>C (p.Asn1335His) c.1230A>C n.880A>C c.799A>C (p.Asn267His) c.883A>C (p.Asn295His) c.2872A>C (p.Asn958His) c.1156A>C (p.Asn386His) | |
2 | g.29197613G>A | CA425433919 | ALK,CLIP4 | c.*607G>A (n.*607G>A) c.4002C>T (p.Ser1334=) c.1229C>T n.879C>T c.798C>T (p.Ser266=) c.882C>T (p.Ser294=) c.2871C>T (p.Ser957=) c.1155C>T (p.Ser385=) | ClinVar dbSNP |
2 | g.29197613G>C | CA346466152 | ALK,CLIP4 | c.*607G>C (n.*607G>C) c.4002C>G (p.Ser1334Arg) c.1229C>G n.879C>G c.798C>G (p.Ser266Arg) c.882C>G (p.Ser294Arg) c.2871C>G (p.Ser957Arg) c.1155C>G (p.Ser385Arg) | ClinVar dbSNP gnomAD v4 |
2 | g.29197613G= | CA1241075377 | ALK,CLIP4 | c.*607G= (n.*607G=) c.4002C= (p.Ser1334=) c.1229C= n.879C= c.798C= (p.Ser266=) c.882C= (p.Ser294=) c.2871C= (p.Ser957=) c.1155C= (p.Ser385=) | |
2 | g.29197613G>T | CA346466154 | ALK,CLIP4 | c.*607G>T (n.*607G>T) c.4002C>A (p.Ser1334Arg) c.1229C>A n.879C>A c.798C>A (p.Ser266Arg) c.882C>A (p.Ser294Arg) c.2871C>A (p.Ser957Arg) c.1155C>A (p.Ser385Arg) | dbSNP |
2 | g.29197614C>A | CA346466162 | ALK,CLIP4 | c.*608C>A (n.*608C>A) c.4001G>T (p.Ser1334Ile) c.1228G>T n.878G>T c.797G>T (p.Ser266Ile) c.881G>T (p.Ser294Ile) c.2870G>T (p.Ser957Ile) c.1154G>T (p.Ser385Ile) | |
2 | g.29197614C= | CA1241075383 | ALK,CLIP4 | c.*608C= (n.*608C=) c.4001G= (p.Ser1334=) c.1228G= n.878G= c.797G= (p.Ser266=) c.881G= (p.Ser294=) c.2870G= (p.Ser957=) c.1154G= (p.Ser385=) | |
2 | g.29197614C>G | CA346466157 | ALK,CLIP4 | c.*608C>G (n.*608C>G) c.4001G>C (p.Ser1334Thr) c.1228G>C n.878G>C c.797G>C (p.Ser266Thr) c.881G>C (p.Ser294Thr) c.2870G>C (p.Ser957Thr) c.1154G>C (p.Ser385Thr) | ClinVar |
2 | g.29197614C>T | CA346466160 | ALK,CLIP4 | c.*608C>T (n.*608C>T) c.4001G>A (p.Ser1334Asn) c.1228G>A n.878G>A c.797G>A (p.Ser266Asn) c.881G>A (p.Ser294Asn) c.2870G>A (p.Ser957Asn) c.1154G>A (p.Ser385Asn) | ClinVar dbSNP gnomAD v4 |
2 | g.29197615T>A | CA346466166 | ALK,CLIP4 | c.*609T>A (n.*609T>A) c.4000A>T (p.Ser1334Cys) c.1227A>T n.877A>T c.796A>T (p.Ser266Cys) c.880A>T (p.Ser294Cys) c.2869A>T (p.Ser957Cys) c.1153A>T (p.Ser385Cys) | ClinVar dbSNP |
2 | g.29197615T>C | CA346466169 | ALK,CLIP4 | c.*609T>C (n.*609T>C) c.4000A>G (p.Ser1334Gly) c.1227A>G n.877A>G c.796A>G (p.Ser266Gly) c.880A>G (p.Ser294Gly) c.2869A>G (p.Ser957Gly) c.1153A>G (p.Ser385Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197615T>G | CA346466170 | ALK,CLIP4 | c.*609T>G (n.*609T>G) c.4000A>C (p.Ser1334Arg) c.1227A>C n.877A>C c.796A>C (p.Ser266Arg) c.880A>C (p.Ser294Arg) c.2869A>C (p.Ser957Arg) c.1153A>C (p.Ser385Arg) | dbSNP |
2 | g.29197615T= | CA1241075389 | ALK,CLIP4 | c.*609T= (n.*609T=) c.4000A= (p.Ser1334=) c.1227A= n.877A= c.796A= (p.Ser266=) c.880A= (p.Ser294=) c.2869A= (p.Ser957=) c.1153A= (p.Ser385=) | |
2 | g.29197616T>A | CA346466172 | ALK,CLIP4 | c.*610T>A (n.*610T>A) c.3999A>T (p.Lys1333Asn) c.1226A>T n.876A>T c.795A>T (p.Lys265Asn) c.879A>T (p.Lys293Asn) c.2868A>T (p.Lys956Asn) c.1152A>T (p.Lys384Asn) | |
2 | g.29197616T>C | CA425433920 | ALK,CLIP4 | c.*610T>C (n.*610T>C) c.3999A>G (p.Lys1333=) c.1226A>G n.876A>G c.795A>G (p.Lys265=) c.879A>G (p.Lys293=) c.2868A>G (p.Lys956=) c.1152A>G (p.Lys384=) | dbSNP |
2 | g.29197616T>G | CA346466175 | ALK,CLIP4 | c.*610T>G (n.*610T>G) c.3999A>C (p.Lys1333Asn) c.1226A>C n.876A>C c.795A>C (p.Lys265Asn) c.879A>C (p.Lys293Asn) c.2868A>C (p.Lys956Asn) c.1152A>C (p.Lys384Asn) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.29197616T= | CA1241075396 | ALK,CLIP4 | c.*610T= (n.*610T=) c.3999A= (p.Lys1333=) c.1226A= n.876A= c.795A= (p.Lys265=) c.879A= (p.Lys293=) c.2868A= (p.Lys956=) c.1152A= (p.Lys384=) | |
2 | g.29197617T>A | CA346466178 | ALK,CLIP4 | c.*611T>A (n.*611T>A) c.3998A>T (p.Lys1333Ile) c.1225A>T n.875A>T c.794A>T (p.Lys265Ile) c.878A>T (p.Lys293Ile) c.2867A>T (p.Lys956Ile) c.1151A>T (p.Lys384Ile) | |
2 | g.29197617T>C | CA346466183 | ALK,CLIP4 | c.*611T>C (n.*611T>C) c.3998A>G (p.Lys1333Arg) c.1225A>G n.875A>G c.794A>G (p.Lys265Arg) c.878A>G (p.Lys293Arg) c.2867A>G (p.Lys956Arg) c.1151A>G (p.Lys384Arg) | dbSNP |
2 | g.29197617T>G | CA346466181 | ALK,CLIP4 | c.*611T>G (n.*611T>G) c.3998A>C (p.Lys1333Thr) c.1225A>C n.875A>C c.794A>C (p.Lys265Thr) c.878A>C (p.Lys293Thr) c.2867A>C (p.Lys956Thr) c.1151A>C (p.Lys384Thr) | ClinVar |
2 | g.29197618T>A | CA346466186 | ALK,CLIP4 | c.*612T>A (n.*612T>A) c.3997A>T (p.Lys1333Ter) c.1224A>T n.874A>T c.793A>T (p.Lys265Ter) c.877A>T (p.Lys293Ter) c.2866A>T (p.Lys956Ter) c.1150A>T (p.Lys384Ter) | dbSNP |
2 | g.29197618T>C | CA346466189 | ALK,CLIP4 | c.*612T>C (n.*612T>C) c.3997A>G (p.Lys1333Glu) c.1224A>G n.874A>G c.793A>G (p.Lys265Glu) c.877A>G (p.Lys293Glu) c.2866A>G (p.Lys956Glu) c.1150A>G (p.Lys384Glu) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.29197618T>G | CA346466191 | ALK,CLIP4 | c.*612T>G (n.*612T>G) c.3997A>C (p.Lys1333Gln) c.1224A>C n.874A>C c.793A>C (p.Lys265Gln) c.877A>C (p.Lys293Gln) c.2866A>C (p.Lys956Gln) c.1150A>C (p.Lys384Gln) | |
2 | g.29197618T= | CA1241075398 | ALK,CLIP4 | c.*612T= (n.*612T=) c.3997A= (p.Lys1333=) c.1224A= n.874A= c.793A= (p.Lys265=) c.877A= (p.Lys293=) c.2866A= (p.Lys956=) c.1150A= (p.Lys384=) | |
2 | g.29197618_29197619delinsTG | CA1241075400 | ALK,CLIP4 | c.*612_*613delinsTG (n.*612_*613delinsTG) c.3996_3997delinsCA (p.Ser1332=) c.1223_1224delinsCA n.873_874delinsCA c.792_793delinsCA (p.Ser264=) c.876_877delinsCA (p.Ser292=) c.2865_2866delinsCA (p.Ser955=) c.1149_1150delinsCA (p.Ser383=) | |
2 | g.29197619del | CA531464589 | ALK,CLIP4 | c.*613del (n.*613del) c.3996del (p.Ser1332ArgfsTer30) c.1223del n.873del c.792del (p.Ser264ArgfsTer30) c.876del (p.Ser292ArgfsTer30) c.2865del (p.Ser955ArgfsTer30) c.1149del (p.Ser383ArgfsTer30) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.29197619G>A | CA425433921 | ALK,CLIP4 | c.*613G>A (n.*613G>A) c.3996C>T (p.Ser1332=) c.1223C>T n.873C>T c.792C>T (p.Ser264=) c.876C>T (p.Ser292=) c.2865C>T (p.Ser955=) c.1149C>T (p.Ser383=) | dbSNP |
2 | g.29197619G>C | CA346466194 | ALK,CLIP4 | c.*613G>C (n.*613G>C) c.3996C>G (p.Ser1332Arg) c.1223C>G n.873C>G c.792C>G (p.Ser264Arg) c.876C>G (p.Ser292Arg) c.2865C>G (p.Ser955Arg) c.1149C>G (p.Ser383Arg) | dbSNP |
2 | g.29197619G>T | CA346466196 | ALK,CLIP4 | c.*613G>T (n.*613G>T) c.3996C>A (p.Ser1332Arg) c.1223C>A n.873C>A c.792C>A (p.Ser264Arg) c.876C>A (p.Ser292Arg) c.2865C>A (p.Ser955Arg) c.1149C>A (p.Ser383Arg) | dbSNP |
2 | g.29197620C>A | CA346466198 | ALK,CLIP4 | c.*614C>A (n.*614C>A) c.3995G>T (p.Ser1332Ile) c.1222G>T n.872G>T c.791G>T (p.Ser264Ile) c.875G>T (p.Ser292Ile) c.2864G>T (p.Ser955Ile) c.1148G>T (p.Ser383Ile) | ClinVar dbSNP gnomAD v4 |
2 | g.29197620C>G | CA346466200 | ALK,CLIP4 | c.*614C>G (n.*614C>G) c.3995G>C (p.Ser1332Thr) c.1222G>C n.872G>C c.791G>C (p.Ser264Thr) c.875G>C (p.Ser292Thr) c.2864G>C (p.Ser955Thr) c.1148G>C (p.Ser383Thr) | dbSNP |
2 | g.29197620C>T | CA346466201 | ALK,CLIP4 | c.*614C>T (n.*614C>T) c.3995G>A (p.Ser1332Asn) c.1222G>A n.872G>A c.791G>A (p.Ser264Asn) c.875G>A (p.Ser292Asn) c.2864G>A (p.Ser955Asn) c.1148G>A (p.Ser383Asn) | dbSNP |
2 | g.29197621T>A | CA346466203 | ALK,CLIP4 | c.*615T>A (n.*615T>A) c.3994A>T (p.Ser1332Cys) c.1221A>T n.871A>T c.790A>T (p.Ser264Cys) c.874A>T (p.Ser292Cys) c.2863A>T (p.Ser955Cys) c.1147A>T (p.Ser383Cys) | |
2 | g.29197621T>C | CA346466206 | ALK,CLIP4 | c.*615T>C (n.*615T>C) c.3994A>G (p.Ser1332Gly) c.1221A>G n.871A>G c.790A>G (p.Ser264Gly) c.874A>G (p.Ser292Gly) c.2863A>G (p.Ser955Gly) c.1147A>G (p.Ser383Gly) | |
2 | g.29197621T>G | CA346466216 | ALK,CLIP4 | c.*615T>G (n.*615T>G) c.3994A>C (p.Ser1332Arg) c.1221A>C n.871A>C c.790A>C (p.Ser264Arg) c.874A>C (p.Ser292Arg) c.2863A>C (p.Ser955Arg) c.1147A>C (p.Ser383Arg) | |
2 | g.29197622G>A | CA425433922 | ALK,CLIP4 | c.*616G>A (n.*616G>A) c.3993C>T (p.Pro1331=) c.1220C>T n.870C>T c.789C>T (p.Pro263=) c.873C>T (p.Pro291=) c.2862C>T (p.Pro954=) c.1146C>T (p.Pro382=) | dbSNP |
2 | g.29197622G>C | CA425433924 | ALK,CLIP4 | c.*616G>C (n.*616G>C) c.3993C>G (p.Pro1331=) c.1220C>G n.870C>G c.789C>G (p.Pro263=) c.873C>G (p.Pro291=) c.2862C>G (p.Pro954=) c.1146C>G (p.Pro382=) | dbSNP |
2 | g.29197622G>T | CA425433923 | ALK,CLIP4 | c.*616G>T (n.*616G>T) c.3993C>A (p.Pro1331=) c.1220C>A n.870C>A c.789C>A (p.Pro263=) c.873C>A (p.Pro291=) c.2862C>A (p.Pro954=) c.1146C>A (p.Pro382=) | dbSNP |
2 | g.29197623G>A | CA346466228 | ALK,CLIP4 | c.*617G>A (n.*617G>A) c.3992C>T (p.Pro1331Leu) c.1219C>T n.869C>T c.788C>T (p.Pro263Leu) c.872C>T (p.Pro291Leu) c.2861C>T (p.Pro954Leu) c.1145C>T (p.Pro382Leu) | ClinVar dbSNP COSMIC |
2 | g.29197623G>C | CA346466229 | ALK,CLIP4 | c.*617G>C (n.*617G>C) c.3992C>G (p.Pro1331Arg) c.1219C>G n.869C>G c.788C>G (p.Pro263Arg) c.872C>G (p.Pro291Arg) c.2861C>G (p.Pro954Arg) c.1145C>G (p.Pro382Arg) | dbSNP |
2 | g.29197623G= | CA1241075407 | ALK,CLIP4 | c.*617G= (n.*617G=) c.3992C= (p.Pro1331=) c.1219C= n.869C= c.788C= (p.Pro263=) c.872C= (p.Pro291=) c.2861C= (p.Pro954=) c.1145C= (p.Pro382=) | |
2 | g.29197623G>T | CA44638105 | ALK,CLIP4 | c.*617G>T (n.*617G>T) c.3992C>A (p.Pro1331His) c.1219C>A n.869C>A c.788C>A (p.Pro263His) c.872C>A (p.Pro291His) c.2861C>A (p.Pro954His) c.1145C>A (p.Pro382His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197624G>A | CA346466238 | ALK,CLIP4 | c.*618G>A (n.*618G>A) c.3991C>T (p.Pro1331Ser) c.1218C>T n.868C>T c.787C>T (p.Pro263Ser) c.871C>T (p.Pro291Ser) c.2860C>T (p.Pro954Ser) c.1144C>T (p.Pro382Ser) | dbSNP |
2 | g.29197624G>C | CA346466235 | ALK,CLIP4 | c.*618G>C (n.*618G>C) c.3991C>G (p.Pro1331Ala) c.1218C>G n.868C>G c.787C>G (p.Pro263Ala) c.871C>G (p.Pro291Ala) c.2860C>G (p.Pro954Ala) c.1144C>G (p.Pro382Ala) | dbSNP |
2 | g.29197624G>T | CA346466237 | ALK,CLIP4 | c.*618G>T (n.*618G>T) c.3991C>A (p.Pro1331Thr) c.1218C>A n.868C>A c.787C>A (p.Pro263Thr) c.871C>A (p.Pro291Thr) c.2860C>A (p.Pro954Thr) c.1144C>A (p.Pro382Thr) | dbSNP |
2 | g.29197625G>A | CA425433925 | ALK,CLIP4 | c.*619G>A (n.*619G>A) c.3990C>T (p.Tyr1330=) c.1217C>T n.867C>T c.786C>T (p.Tyr262=) c.870C>T (p.Tyr290=) c.2859C>T (p.Tyr953=) c.1143C>T (p.Tyr381=) | dbSNP |
2 | g.29197625G>C | CA346466239 | ALK,CLIP4 | c.*619G>C (n.*619G>C) c.3990C>G (p.Tyr1330Ter) c.1217C>G n.867C>G c.786C>G (p.Tyr262Ter) c.870C>G (p.Tyr290Ter) c.2859C>G (p.Tyr953Ter) c.1143C>G (p.Tyr381Ter) | dbSNP |
2 | g.29197625G>T | CA346466240 | ALK,CLIP4 | c.*619G>T (n.*619G>T) c.3990C>A (p.Tyr1330Ter) c.1217C>A n.867C>A c.786C>A (p.Tyr262Ter) c.870C>A (p.Tyr290Ter) c.2859C>A (p.Tyr953Ter) c.1143C>A (p.Tyr381Ter) | ClinVar dbSNP |
2 | g.29197626T>A | CA346466241 | ALK,CLIP4 | c.*620T>A (n.*620T>A) c.3989A>T (p.Tyr1330Phe) c.1216A>T n.866A>T c.785A>T (p.Tyr262Phe) c.869A>T (p.Tyr290Phe) c.2858A>T (p.Tyr953Phe) c.1142A>T (p.Tyr381Phe) | dbSNP |
2 | g.29197626T>C | CA346466242 | ALK,CLIP4 | c.*620T>C (n.*620T>C) c.3989A>G (p.Tyr1330Cys) c.1216A>G n.866A>G c.785A>G (p.Tyr262Cys) c.869A>G (p.Tyr290Cys) c.2858A>G (p.Tyr953Cys) c.1142A>G (p.Tyr381Cys) | dbSNP |
2 | g.29197626T>G | CA346466243 | ALK,CLIP4 | c.*620T>G (n.*620T>G) c.3989A>C (p.Tyr1330Ser) c.1216A>C n.866A>C c.785A>C (p.Tyr262Ser) c.869A>C (p.Tyr290Ser) c.2858A>C (p.Tyr953Ser) c.1142A>C (p.Tyr381Ser) | dbSNP |
2 | g.29197627A= | CA1241075415 | ALK,CLIP4 | c.*621A= (n.*621A=) c.3988T= (p.Tyr1330=) c.1215T= n.865T= c.784T= (p.Tyr262=) c.868T= (p.Tyr290=) c.2857T= (p.Tyr953=) c.1141T= (p.Tyr381=) | |
2 | g.29197627A>C | CA346466244 | ALK,CLIP4 | c.*621A>C (n.*621A>C) c.3988T>G (p.Tyr1330Asp) c.1215T>G n.865T>G c.784T>G (p.Tyr262Asp) c.868T>G (p.Tyr290Asp) c.2857T>G (p.Tyr953Asp) c.1141T>G (p.Tyr381Asp) | |
2 | g.29197627A>G | CA346466246 | ALK,CLIP4 | c.*621A>G (n.*621A>G) c.3988T>C (p.Tyr1330His) c.1215T>C n.865T>C c.784T>C (p.Tyr262His) c.868T>C (p.Tyr290His) c.2857T>C (p.Tyr953His) c.1141T>C (p.Tyr381His) | ClinVar dbSNP |
2 | g.29197627A>T | CA346466248 | ALK,CLIP4 | c.*621A>T (n.*621A>T) c.3988T>A (p.Tyr1330Asn) c.1215T>A n.865T>A c.784T>A (p.Tyr262Asn) c.868T>A (p.Tyr290Asn) c.2857T>A (p.Tyr953Asn) c.1141T>A (p.Tyr381Asn) | dbSNP |
2 | g.29197628T>A | CA425433926 | ALK,CLIP4 | c.*622T>A (n.*622T>A) c.3987A>T (p.Pro1329=) c.1214A>T n.864A>T c.783A>T (p.Pro261=) c.867A>T (p.Pro289=) c.2856A>T (p.Pro952=) c.1140A>T (p.Pro380=) | |
2 | g.29197628T>C | CA425433927 | ALK,CLIP4 | c.*622T>C (n.*622T>C) c.3987A>G (p.Pro1329=) c.1214A>G n.864A>G c.783A>G (p.Pro261=) c.867A>G (p.Pro289=) c.2856A>G (p.Pro952=) c.1140A>G (p.Pro380=) | ClinVar gnomAD v4 |
2 | g.29197628T>G | CA425433928 | ALK,CLIP4 | c.*622T>G (n.*622T>G) c.3987A>C (p.Pro1329=) c.1214A>C n.864A>C c.783A>C (p.Pro261=) c.867A>C (p.Pro289=) c.2856A>C (p.Pro952=) c.1140A>C (p.Pro380=) | |
2 | g.29197629G>A | CA346466250 | ALK,CLIP4 | c.*623G>A (n.*623G>A) c.3986C>T (p.Pro1329Leu) c.1213C>T n.863C>T c.782C>T (p.Pro261Leu) c.866C>T (p.Pro289Leu) c.2855C>T (p.Pro952Leu) c.1139C>T (p.Pro380Leu) | ClinVar dbSNP |
2 | g.29197629G>C | CA346466259 | ALK,CLIP4 | c.*623G>C (n.*623G>C) c.3986C>G (p.Pro1329Arg) c.1213C>G n.863C>G c.782C>G (p.Pro261Arg) c.866C>G (p.Pro289Arg) c.2855C>G (p.Pro952Arg) c.1139C>G (p.Pro380Arg) | dbSNP |
2 | g.29197629G>T | CA346466260 | ALK,CLIP4 | c.*623G>T (n.*623G>T) c.3986C>A (p.Pro1329Gln) c.1213C>A n.863C>A c.782C>A (p.Pro261Gln) c.866C>A (p.Pro289Gln) c.2855C>A (p.Pro952Gln) c.1139C>A (p.Pro380Gln) | dbSNP |
2 | g.29197630G>A | CA44638109 | ALK,CLIP4 | c.*624G>A (n.*624G>A) c.3985C>T (p.Pro1329Ser) c.1212C>T n.862C>T c.781C>T (p.Pro261Ser) c.865C>T (p.Pro289Ser) c.2854C>T (p.Pro952Ser) c.1138C>T (p.Pro380Ser) | ClinVar dbSNP |
2 | g.29197630G>C | CA346466266 | ALK,CLIP4 | c.*624G>C (n.*624G>C) c.3985C>G (p.Pro1329Ala) c.1212C>G n.862C>G c.781C>G (p.Pro261Ala) c.865C>G (p.Pro289Ala) c.2854C>G (p.Pro952Ala) c.1138C>G (p.Pro380Ala) | dbSNP |
2 | g.29197630G= | CA1241075421 | ALK,CLIP4 | c.*624G= (n.*624G=) c.3985C= (p.Pro1329=) c.1212C= n.862C= c.781C= (p.Pro261=) c.865C= (p.Pro289=) c.2854C= (p.Pro952=) c.1138C= (p.Pro380=) | |
2 | g.29197630G>T | CA346466264 | ALK,CLIP4 | c.*624G>T (n.*624G>T) c.3985C>A (p.Pro1329Thr) c.1212C>A n.862C>A c.781C>A (p.Pro261Thr) c.865C>A (p.Pro289Thr) c.2854C>A (p.Pro952Thr) c.1138C>A (p.Pro380Thr) | dbSNP |
2 | g.29197631C>A | CA346466268 | ALK,CLIP4 | c.*625C>A (n.*625C>A) c.3984G>T (p.Met1328Ile) c.1211G>T n.861G>T c.780G>T (p.Met260Ile) c.864G>T (p.Met288Ile) c.2853G>T (p.Met951Ile) c.1137G>T (p.Met379Ile) | dbSNP |
2 | g.29197631C= | CA1241075424 | ALK,CLIP4 | c.*625C= (n.*625C=) c.3984G= (p.Met1328=) c.1211G= n.861G= c.780G= (p.Met260=) c.864G= (p.Met288=) c.2853G= (p.Met951=) c.1137G= (p.Met379=) | |
2 | g.29197631C>G | CA346466270 | ALK,CLIP4 | c.*625C>G (n.*625C>G) c.3984G>C (p.Met1328Ile) c.1211G>C n.861G>C c.780G>C (p.Met260Ile) c.864G>C (p.Met288Ile) c.2853G>C (p.Met951Ile) c.1137G>C (p.Met379Ile) | dbSNP |
2 | g.29197631C>T | CA10581961 | ALK,CLIP4 | c.*625C>T (n.*625C>T) c.3984G>A (p.Met1328Ile) c.1211G>A n.861G>A c.780G>A (p.Met260Ile) c.864G>A (p.Met288Ile) c.2853G>A (p.Met951Ile) c.1137G>A (p.Met379Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197632A>C | CA346466275 | ALK,CLIP4 | c.*626A>C (n.*626A>C) c.3983T>G (p.Met1328Arg) c.1210T>G n.860T>G c.779T>G (p.Met260Arg) c.863T>G (p.Met288Arg) c.2852T>G (p.Met951Arg) c.1136T>G (p.Met379Arg) | |
2 | g.29197632A>G | CA346466277 | ALK,CLIP4 | c.*626A>G (n.*626A>G) c.3983T>C (p.Met1328Thr) c.1210T>C n.860T>C c.779T>C (p.Met260Thr) c.863T>C (p.Met288Thr) c.2852T>C (p.Met951Thr) c.1136T>C (p.Met379Thr) | ClinVar dbSNP |
2 | g.29197632A>T | CA346466280 | ALK,CLIP4 | c.*626A>T (n.*626A>T) c.3983T>A (p.Met1328Lys) c.1210T>A n.860T>A c.779T>A (p.Met260Lys) c.863T>A (p.Met288Lys) c.2852T>A (p.Met951Lys) c.1136T>A (p.Met379Lys) | dbSNP |
2 | g.29197633T>A | CA44638112 | ALK,CLIP4 | c.*627T>A (n.*627T>A) c.3982A>T (p.Met1328Leu) c.1209A>T n.859A>T c.778A>T (p.Met260Leu) c.862A>T (p.Met288Leu) c.2851A>T (p.Met951Leu) c.1135A>T (p.Met379Leu) | dbSNP |
2 | g.29197633T>C | CA346466284 | ALK,CLIP4 | c.*627T>C (n.*627T>C) c.3982A>G (p.Met1328Val) c.1209A>G n.859A>G c.778A>G (p.Met260Val) c.862A>G (p.Met288Val) c.2851A>G (p.Met951Val) c.1135A>G (p.Met379Val) | dbSNP |
2 | g.29197633T>G | CA346466288 | ALK,CLIP4 | c.*627T>G (n.*627T>G) c.3982A>C (p.Met1328Leu) c.1209A>C n.859A>C c.778A>C (p.Met260Leu) c.862A>C (p.Met288Leu) c.2851A>C (p.Met951Leu) c.1135A>C (p.Met379Leu) | dbSNP |
2 | g.29197633T= | CA1241075428 | ALK,CLIP4 | c.*627T= (n.*627T=) c.3982A= (p.Met1328=) c.1209A= n.859A= c.778A= (p.Met260=) c.862A= (p.Met288=) c.2851A= (p.Met951=) c.1135A= (p.Met379=) | |
2 | g.29197634A= | CA1241075430 | ALK,CLIP4 | c.*628A= (n.*628A=) c.3981T= (p.Tyr1327=) c.1208T= n.858T= c.777T= (p.Tyr259=) c.861T= (p.Tyr287=) c.2850T= (p.Tyr950=) c.1134T= (p.Tyr378=) | |
2 | g.29197634A>C | CA346466290 | ALK,CLIP4 | c.*628A>C (n.*628A>C) c.3981T>G (p.Tyr1327Ter) c.1208T>G n.858T>G c.777T>G (p.Tyr259Ter) c.861T>G (p.Tyr287Ter) c.2850T>G (p.Tyr950Ter) c.1134T>G (p.Tyr378Ter) | ClinVar dbSNP gnomAD v4 |
2 | g.29197634A>G | CA425433929 | ALK,CLIP4 | c.*628A>G (n.*628A>G) c.3981T>C (p.Tyr1327=) c.1208T>C n.858T>C c.777T>C (p.Tyr259=) c.861T>C (p.Tyr287=) c.2850T>C (p.Tyr950=) c.1134T>C (p.Tyr378=) | dbSNP |
2 | g.29197634A>T | CA346466291 | ALK,CLIP4 | c.*628A>T (n.*628A>T) c.3981T>A (p.Tyr1327Ter) c.1208T>A n.858T>A c.777T>A (p.Tyr259Ter) c.861T>A (p.Tyr287Ter) c.2850T>A (p.Tyr950Ter) c.1134T>A (p.Tyr378Ter) | dbSNP |
2 | g.29197635T>A | CA346466297 | ALK,CLIP4 | c.*629T>A (n.*629T>A) c.3980A>T (p.Tyr1327Phe) c.1207A>T n.857A>T c.776A>T (p.Tyr259Phe) c.860A>T (p.Tyr287Phe) c.2849A>T (p.Tyr950Phe) c.1133A>T (p.Tyr378Phe) | dbSNP |
2 | g.29197635T>C | CA346466299 | ALK,CLIP4 | c.*629T>C (n.*629T>C) c.3980A>G (p.Tyr1327Cys) c.1207A>G n.857A>G c.776A>G (p.Tyr259Cys) c.860A>G (p.Tyr287Cys) c.2849A>G (p.Tyr950Cys) c.1133A>G (p.Tyr378Cys) | dbSNP gnomAD v4 |
2 | g.29197635T>G | CA346466293 | ALK,CLIP4 | c.*629T>G (n.*629T>G) c.3980A>C (p.Tyr1327Ser) c.1207A>C n.857A>C c.776A>C (p.Tyr259Ser) c.860A>C (p.Tyr287Ser) c.2849A>C (p.Tyr950Ser) c.1133A>C (p.Tyr378Ser) | dbSNP |
2 | g.29197635T= | CA1241075432 | ALK,CLIP4 | c.*629T= (n.*629T=) c.3980A= (p.Tyr1327=) c.1207A= n.857A= c.776A= (p.Tyr259=) c.860A= (p.Tyr287=) c.2849A= (p.Tyr950=) c.1133A= (p.Tyr378=) | |
2 | g.29197636A>C | CA346466301 | ALK,CLIP4 | c.*630A>C (n.*630A>C) c.3979T>G (p.Tyr1327Asp) c.1206T>G n.856T>G c.775T>G (p.Tyr259Asp) c.859T>G (p.Tyr287Asp) c.2848T>G (p.Tyr950Asp) c.1132T>G (p.Tyr378Asp) | dbSNP |
2 | g.29197636A>G | CA346466302 | ALK,CLIP4 | c.*630A>G (n.*630A>G) c.3979T>C (p.Tyr1327His) c.1206T>C n.856T>C c.775T>C (p.Tyr259His) c.859T>C (p.Tyr287His) c.2848T>C (p.Tyr950His) c.1132T>C (p.Tyr378His) | dbSNP |
2 | g.29197636A>T | CA346466304 | ALK,CLIP4 | c.*630A>T (n.*630A>T) c.3979T>A (p.Tyr1327Asn) c.1206T>A n.856T>A c.775T>A (p.Tyr259Asn) c.859T>A (p.Tyr287Asn) c.2848T>A (p.Tyr950Asn) c.1132T>A (p.Tyr378Asn) | dbSNP |
2 | g.29197637T>A | CA425433930 | ALK,CLIP4 | c.*631T>A (n.*631T>A) c.3978A>T (p.Gly1326=) c.1205A>T n.855A>T c.774A>T (p.Gly258=) c.858A>T (p.Gly286=) c.2847A>T (p.Gly949=) c.1131A>T (p.Gly377=) | |
2 | g.29197637T>C | CA44638113 | ALK,CLIP4 | c.*631T>C (n.*631T>C) c.3978A>G (p.Gly1326=) c.1205A>G n.855A>G c.774A>G (p.Gly258=) c.858A>G (p.Gly286=) c.2847A>G (p.Gly949=) c.1131A>G (p.Gly377=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197637T>G | CA425433931 | ALK,CLIP4 | c.*631T>G (n.*631T>G) c.3978A>C (p.Gly1326=) c.1205A>C n.855A>C c.774A>C (p.Gly258=) c.858A>C (p.Gly286=) c.2847A>C (p.Gly949=) c.1131A>C (p.Gly377=) | |
2 | g.29197637T= | CA1241075437 | ALK,CLIP4 | c.*631T= (n.*631T=) c.3978A= (p.Gly1326=) c.1205A= n.855A= c.774A= (p.Gly258=) c.858A= (p.Gly286=) c.2847A= (p.Gly949=) c.1131A= (p.Gly377=) | |
2 | g.29197638C>A | CA346466310 | ALK,CLIP4 | c.*632C>A (n.*632C>A) c.3977G>T (p.Gly1326Val) c.1204G>T n.854G>T c.773G>T (p.Gly258Val) c.857G>T (p.Gly286Val) c.2846G>T (p.Gly949Val) c.1130G>T (p.Gly377Val) | dbSNP |
2 | g.29197638C>G | CA346466311 | ALK,CLIP4 | c.*632C>G (n.*632C>G) c.3977G>C (p.Gly1326Ala) c.1204G>C n.854G>C c.773G>C (p.Gly258Ala) c.857G>C (p.Gly286Ala) c.2846G>C (p.Gly949Ala) c.1130G>C (p.Gly377Ala) | dbSNP |
2 | g.29197638C>T | CA346466314 | ALK,CLIP4 | c.*632C>T (n.*632C>T) c.3977G>A (p.Gly1326Glu) c.1204G>A n.854G>A c.773G>A (p.Gly258Glu) c.857G>A (p.Gly286Glu) c.2846G>A (p.Gly949Glu) c.1130G>A (p.Gly377Glu) | dbSNP COSMIC |
2 | g.29197639del | CA2698954158 | ALK,CLIP4 | c.*633del (n.*633del) c.3977del (p.Gly1326AspfsTer?) c.1204del n.854del c.773del (p.Gly258AspfsTer?) c.857del (p.Gly286AspfsTer?) c.2846del (p.Gly949AspfsTer?) c.1130del (p.Gly377AspfsTer?) | dbSNP |
2 | g.29197639C>A | CA346466316 | ALK,CLIP4 | c.*633C>A (n.*633C>A) c.3976G>T (p.Gly1326Ter) c.1203G>T n.853G>T c.772G>T (p.Gly258Ter) c.856G>T (p.Gly286Ter) c.2845G>T (p.Gly949Ter) c.1129G>T (p.Gly377Ter) | dbSNP |
2 | g.29197639C>G | CA346466320 | ALK,CLIP4 | c.*633C>G (n.*633C>G) c.3976G>C (p.Gly1326Arg) c.1203G>C n.853G>C c.772G>C (p.Gly258Arg) c.856G>C (p.Gly286Arg) c.2845G>C (p.Gly949Arg) c.1129G>C (p.Gly377Arg) | dbSNP |
2 | g.29197639C>T | CA346466323 | ALK,CLIP4 | c.*633C>T (n.*633C>T) c.3976G>A (p.Gly1326Arg) c.1203G>A n.853G>A c.772G>A (p.Gly258Arg) c.856G>A (p.Gly286Arg) c.2845G>A (p.Gly949Arg) c.1129G>A (p.Gly377Arg) | dbSNP |
2 | g.29197640A>C | CA425433932 | ALK,CLIP4 | c.*634A>C (n.*634A>C) c.3975T>G (p.Leu1325=) c.1202T>G n.852T>G c.771T>G (p.Leu257=) c.855T>G (p.Leu285=) c.2844T>G (p.Leu948=) c.1128T>G (p.Leu376=) | |
2 | g.29197640A>G | CA425433933 | ALK,CLIP4 | c.*634A>G (n.*634A>G) c.3975T>C (p.Leu1325=) c.1202T>C n.852T>C c.771T>C (p.Leu257=) c.855T>C (p.Leu285=) c.2844T>C (p.Leu948=) c.1128T>C (p.Leu376=) | ClinVar dbSNP |
2 | g.29197640A>T | CA425433934 | ALK,CLIP4 | c.*634A>T (n.*634A>T) c.3975T>A (p.Leu1325=) c.1202T>A n.852T>A c.771T>A (p.Leu257=) c.855T>A (p.Leu285=) c.2844T>A (p.Leu948=) c.1128T>A (p.Leu376=) | dbSNP |
2 | g.29197641A>C | CA346466324 | ALK,CLIP4 | c.*635A>C (n.*635A>C) c.3974T>G (p.Leu1325Arg) c.1201T>G n.851T>G c.770T>G (p.Leu257Arg) c.854T>G (p.Leu285Arg) c.2843T>G (p.Leu948Arg) c.1127T>G (p.Leu376Arg) | |
2 | g.29197641A>G | CA346466326 | ALK,CLIP4 | c.*635A>G (n.*635A>G) c.3974T>C (p.Leu1325Pro) c.1201T>C n.851T>C c.770T>C (p.Leu257Pro) c.854T>C (p.Leu285Pro) c.2843T>C (p.Leu948Pro) c.1127T>C (p.Leu376Pro) | ClinVar dbSNP |
2 | g.29197641A>T | CA346466327 | ALK,CLIP4 | c.*635A>T (n.*635A>T) c.3974T>A (p.Leu1325His) c.1201T>A n.851T>A c.770T>A (p.Leu257His) c.854T>A (p.Leu285His) c.2843T>A (p.Leu948His) c.1127T>A (p.Leu376His) | dbSNP gnomAD v4 |
2 | g.29197642G>A | CA346466330 | ALK,CLIP4 | c.*636G>A (n.*636G>A) c.3973C>T (p.Leu1325Phe) c.1200C>T n.850C>T c.769C>T (p.Leu257Phe) c.853C>T (p.Leu285Phe) c.2842C>T (p.Leu948Phe) c.1126C>T (p.Leu376Phe) | dbSNP |
2 | g.29197642G>C | CA346466329 | ALK,CLIP4 | c.*636G>C (n.*636G>C) c.3973C>G (p.Leu1325Val) c.1200C>G n.850C>G c.769C>G (p.Leu257Val) c.853C>G (p.Leu285Val) c.2842C>G (p.Leu948Val) c.1126C>G (p.Leu376Val) | dbSNP |
2 | g.29197642G>T | CA346466328 | ALK,CLIP4 | c.*636G>T (n.*636G>T) c.3973C>A (p.Leu1325Ile) c.1200C>A n.850C>A c.769C>A (p.Leu257Ile) c.853C>A (p.Leu285Ile) c.2842C>A (p.Leu948Ile) c.1126C>A (p.Leu376Ile) | dbSNP |
2 | g.29197643A>C | CA425433935 | ALK,CLIP4 | c.*637A>C (n.*637A>C) c.3972T>G (p.Ser1324=) c.1199T>G n.849T>G c.768T>G (p.Ser256=) c.852T>G (p.Ser284=) c.2841T>G (p.Ser947=) c.1125T>G (p.Ser375=) | |
2 | g.29197643A>G | CA425433936 | ALK,CLIP4 | c.*637A>G (n.*637A>G) c.3972T>C (p.Ser1324=) c.1199T>C n.849T>C c.768T>C (p.Ser256=) c.852T>C (p.Ser284=) c.2841T>C (p.Ser947=) c.1125T>C (p.Ser375=) | dbSNP |
2 | g.29197643A>T | CA425433937 | ALK,CLIP4 | c.*637A>T (n.*637A>T) c.3972T>A (p.Ser1324=) c.1199T>A n.849T>A c.768T>A (p.Ser256=) c.852T>A (p.Ser284=) c.2841T>A (p.Ser947=) c.1125T>A (p.Ser375=) | ClinVar dbSNP |
2 | g.29197644G>A | CA346466332 | ALK,CLIP4 | c.*638G>A (n.*638G>A) c.3971C>T (p.Ser1324Phe) c.1198C>T n.848C>T c.767C>T (p.Ser256Phe) c.851C>T (p.Ser284Phe) c.2840C>T (p.Ser947Phe) c.1124C>T (p.Ser375Phe) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
2 | g.29197644G>C | CA1593706 | ALK,CLIP4 | c.*638G>C (n.*638G>C) c.3971C>G (p.Ser1324Cys) c.1198C>G n.848C>G c.767C>G (p.Ser256Cys) c.851C>G (p.Ser284Cys) c.2840C>G (p.Ser947Cys) c.1124C>G (p.Ser375Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29197644G= | CA1241075445 | ALK,CLIP4 | c.*638G= (n.*638G=) c.3971C= (p.Ser1324=) c.1198C= n.848C= c.767C= (p.Ser256=) c.851C= (p.Ser284=) c.2840C= (p.Ser947=) c.1124C= (p.Ser375=) | |
2 | g.29197644G>T | CA346466335 | ALK,CLIP4 | c.*638G>T (n.*638G>T) c.3971C>A (p.Ser1324Tyr) c.1198C>A n.848C>A c.767C>A (p.Ser256Tyr) c.851C>A (p.Ser284Tyr) c.2840C>A (p.Ser947Tyr) c.1124C>A (p.Ser375Tyr) | |
2 | g.29197645A>C | CA346466337 | ALK,CLIP4 | c.*639A>C (n.*639A>C) c.3970T>G (p.Ser1324Ala) c.1197T>G n.847T>G c.766T>G (p.Ser256Ala) c.850T>G (p.Ser284Ala) c.2839T>G (p.Ser947Ala) c.1123T>G (p.Ser375Ala) | |
2 | g.29197645A>G | CA346466338 | ALK,CLIP4 | c.*639A>G (n.*639A>G) c.3970T>C (p.Ser1324Pro) c.1197T>C n.847T>C c.766T>C (p.Ser256Pro) c.850T>C (p.Ser284Pro) c.2839T>C (p.Ser947Pro) c.1123T>C (p.Ser375Pro) | dbSNP |
2 | g.29197645A>T | CA346466343 | ALK,CLIP4 | c.*639A>T (n.*639A>T) c.3970T>A (p.Ser1324Thr) c.1197T>A n.847T>A c.766T>A (p.Ser256Thr) c.850T>A (p.Ser284Thr) c.2839T>A (p.Ser947Thr) c.1123T>A (p.Ser375Thr) | dbSNP |
2 | g.29197646A= | CA1241075452 | ALK,CLIP4 | c.*640A= (n.*640A=) c.3969T= (p.Phe1323=) c.1196T= n.846T= c.765T= (p.Phe255=) c.849T= (p.Phe283=) c.2838T= (p.Phe946=) c.1122T= (p.Phe374=) | |
2 | g.29197646A>C | CA346466344 | ALK,CLIP4 | c.*640A>C (n.*640A>C) c.3969T>G (p.Phe1323Leu) c.1196T>G n.846T>G c.765T>G (p.Phe255Leu) c.849T>G (p.Phe283Leu) c.2838T>G (p.Phe946Leu) c.1122T>G (p.Phe374Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.29197646A>G | CA425433938 | ALK,CLIP4 | c.*640A>G (n.*640A>G) c.3969T>C (p.Phe1323=) c.1196T>C n.846T>C c.765T>C (p.Phe255=) c.849T>C (p.Phe283=) c.2838T>C (p.Phe946=) c.1122T>C (p.Phe374=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197646A>T | CA346466345 | ALK,CLIP4 | c.*640A>T (n.*640A>T) c.3969T>A (p.Phe1323Leu) c.1196T>A n.846T>A c.765T>A (p.Phe255Leu) c.849T>A (p.Phe283Leu) c.2838T>A (p.Phe946Leu) c.1122T>A (p.Phe374Leu) | dbSNP |
2 | g.29197647A= | CA1241075458 | ALK,CLIP4 | c.*641A= (n.*641A=) c.3968T= (p.Phe1323=) c.1195T= n.845T= c.764T= (p.Phe255=) c.848T= (p.Phe283=) c.2837T= (p.Phe946=) c.1121T= (p.Phe374=) | |
2 | g.29197647A>C | CA346466347 | ALK,CLIP4 | c.*641A>C (n.*641A>C) c.3968T>G (p.Phe1323Cys) c.1195T>G n.845T>G c.764T>G (p.Phe255Cys) c.848T>G (p.Phe283Cys) c.2837T>G (p.Phe946Cys) c.1121T>G (p.Phe374Cys) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197647A>G | CA346466349 | ALK,CLIP4 | c.*641A>G (n.*641A>G) c.3968T>C (p.Phe1323Ser) c.1195T>C n.845T>C c.764T>C (p.Phe255Ser) c.848T>C (p.Phe283Ser) c.2837T>C (p.Phe946Ser) c.1121T>C (p.Phe374Ser) | ClinVar dbSNP |
2 | g.29197647A>T | CA346466350 | ALK,CLIP4 | c.*641A>T (n.*641A>T) c.3968T>A (p.Phe1323Tyr) c.1195T>A n.845T>A c.764T>A (p.Phe255Tyr) c.848T>A (p.Phe283Tyr) c.2837T>A (p.Phe946Tyr) c.1121T>A (p.Phe374Tyr) | dbSNP |
2 | g.29197648A>C | CA346466351 | ALK,CLIP4 | c.*642A>C (n.*642A>C) c.3967T>G (p.Phe1323Val) c.1194T>G n.844T>G c.763T>G (p.Phe255Val) c.847T>G (p.Phe283Val) c.2836T>G (p.Phe946Val) c.1120T>G (p.Phe374Val) | |
2 | g.29197648A>G | CA346466353 | ALK,CLIP4 | c.*642A>G (n.*642A>G) c.3967T>C (p.Phe1323Leu) c.1194T>C n.844T>C c.763T>C (p.Phe255Leu) c.847T>C (p.Phe283Leu) c.2836T>C (p.Phe946Leu) c.1120T>C (p.Phe374Leu) | dbSNP |
2 | g.29197648A>T | CA346466356 | ALK,CLIP4 | c.*642A>T (n.*642A>T) c.3967T>A (p.Phe1323Ile) c.1194T>A n.844T>A c.763T>A (p.Phe255Ile) c.847T>A (p.Phe283Ile) c.2836T>A (p.Phe946Ile) c.1120T>A (p.Phe374Ile) | dbSNP |
2 | g.29197649G>A | CA425433939 | ALK,CLIP4 | c.*643G>A (n.*643G>A) c.3966C>T (p.Ile1322=) c.1193C>T n.843C>T c.762C>T (p.Ile254=) c.846C>T (p.Ile282=) c.2835C>T (p.Ile945=) c.1119C>T (p.Ile373=) | dbSNP |
2 | g.29197649G>C | CA346466359 | ALK,CLIP4 | c.*643G>C (n.*643G>C) c.3966C>G (p.Ile1322Met) c.1193C>G n.843C>G c.762C>G (p.Ile254Met) c.846C>G (p.Ile282Met) c.2835C>G (p.Ile945Met) c.1119C>G (p.Ile373Met) | ClinVar dbSNP |
2 | g.29197649G>T | CA425433940 | ALK,CLIP4 | c.*643G>T (n.*643G>T) c.3966C>A (p.Ile1322=) c.1193C>A n.843C>A c.762C>A (p.Ile254=) c.846C>A (p.Ile282=) c.2835C>A (p.Ile945=) c.1119C>A (p.Ile373=) | ClinVar dbSNP gnomAD v4 COSMIC |
2 | g.29197650A>C | CA346466363 | ALK,CLIP4 | c.*644A>C (n.*644A>C) c.3965T>G (p.Ile1322Ser) c.1192T>G n.842T>G c.761T>G (p.Ile254Ser) c.845T>G (p.Ile282Ser) c.2834T>G (p.Ile945Ser) c.1118T>G (p.Ile373Ser) | dbSNP |
2 | g.29197650A>G | CA346466361 | ALK,CLIP4 | c.*644A>G (n.*644A>G) c.3965T>C (p.Ile1322Thr) c.1192T>C n.842T>C c.761T>C (p.Ile254Thr) c.845T>C (p.Ile282Thr) c.2834T>C (p.Ile945Thr) c.1118T>C (p.Ile373Thr) | |
2 | g.29197650A>T | CA346466365 | ALK,CLIP4 | c.*644A>T (n.*644A>T) c.3965T>A (p.Ile1322Asn) c.1192T>A n.842T>A c.761T>A (p.Ile254Asn) c.845T>A (p.Ile282Asn) c.2834T>A (p.Ile945Asn) c.1118T>A (p.Ile373Asn) | ClinVar dbSNP |
2 | g.29197651T>A | CA346466368 | ALK,CLIP4 | c.*645T>A (n.*645T>A) c.3964A>T (p.Ile1322Phe) c.1191A>T n.841A>T c.760A>T (p.Ile254Phe) c.844A>T (p.Ile282Phe) c.2833A>T (p.Ile945Phe) c.1117A>T (p.Ile373Phe) | dbSNP |
2 | g.29197651T>C | CA346466373 | ALK,CLIP4 | c.*645T>C (n.*645T>C) c.3964A>G (p.Ile1322Val) c.1191A>G n.841A>G c.760A>G (p.Ile254Val) c.844A>G (p.Ile282Val) c.2833A>G (p.Ile945Val) c.1117A>G (p.Ile373Val) | dbSNP |
2 | g.29197651T>G | CA346466371 | ALK,CLIP4 | c.*645T>G (n.*645T>G) c.3964A>C (p.Ile1322Leu) c.1191A>C n.841A>C c.760A>C (p.Ile254Leu) c.844A>C (p.Ile282Leu) c.2833A>C (p.Ile945Leu) c.1117A>C (p.Ile373Leu) | dbSNP |
2 | g.29197652T>A | CA346466375 | ALK,CLIP4 | c.*646T>A (n.*646T>A) c.3963A>T (p.Glu1321Asp) c.1190A>T n.840A>T c.759A>T (p.Glu253Asp) c.843A>T (p.Glu281Asp) c.2832A>T (p.Glu944Asp) c.1116A>T (p.Glu372Asp) | dbSNP |
2 | g.29197652T>C | CA425433941 | ALK,CLIP4 | c.*646T>C (n.*646T>C) c.3963A>G (p.Glu1321=) c.1190A>G n.840A>G c.759A>G (p.Glu253=) c.843A>G (p.Glu281=) c.2832A>G (p.Glu944=) c.1116A>G (p.Glu372=) | dbSNP |
2 | g.29197652T>G | CA346466378 | ALK,CLIP4 | c.*646T>G (n.*646T>G) c.3963A>C (p.Glu1321Asp) c.1190A>C n.840A>C c.759A>C (p.Glu253Asp) c.843A>C (p.Glu281Asp) c.2832A>C (p.Glu944Asp) c.1116A>C (p.Glu372Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197652T= | CA1241075460 | ALK,CLIP4 | c.*646T= (n.*646T=) c.3963A= (p.Glu1321=) c.1190A= n.840A= c.759A= (p.Glu253=) c.843A= (p.Glu281=) c.2832A= (p.Glu944=) c.1116A= (p.Glu372=) | |
2 | g.29197653T>A | CA346466387 | ALK,CLIP4 | c.*647T>A (n.*647T>A) c.3962A>T (p.Glu1321Val) c.1189A>T n.839A>T c.758A>T (p.Glu253Val) c.842A>T (p.Glu281Val) c.2831A>T (p.Glu944Val) c.1115A>T (p.Glu372Val) | COSMIC |
2 | g.29197653T>C | CA346466392 | ALK,CLIP4 | c.*647T>C (n.*647T>C) c.3962A>G (p.Glu1321Gly) c.1189A>G n.839A>G c.758A>G (p.Glu253Gly) c.842A>G (p.Glu281Gly) c.2831A>G (p.Glu944Gly) c.1115A>G (p.Glu372Gly) | |
2 | g.29197653T>G | CA346466390 | ALK,CLIP4 | c.*647T>G (n.*647T>G) c.3962A>C (p.Glu1321Ala) c.1189A>C n.839A>C c.758A>C (p.Glu253Ala) c.842A>C (p.Glu281Ala) c.2831A>C (p.Glu944Ala) c.1115A>C (p.Glu372Ala) | |
2 | g.29197654C>A | CA346466394 | ALK,CLIP4 | c.*648C>A (n.*648C>A) c.3961G>T (p.Glu1321Ter) c.1188G>T n.838G>T c.757G>T (p.Glu253Ter) c.841G>T (p.Glu281Ter) c.2830G>T (p.Glu944Ter) c.1114G>T (p.Glu372Ter) | dbSNP |
2 | g.29197654C>G | CA346466395 | ALK,CLIP4 | c.*648C>G (n.*648C>G) c.3961G>C (p.Glu1321Gln) c.1188G>C n.838G>C c.757G>C (p.Glu253Gln) c.841G>C (p.Glu281Gln) c.2830G>C (p.Glu944Gln) c.1114G>C (p.Glu372Gln) | dbSNP |
2 | g.29197654C>T | CA346466396 | ALK,CLIP4 | c.*648C>T (n.*648C>T) c.3961G>A (p.Glu1321Lys) c.1188G>A n.838G>A c.757G>A (p.Glu253Lys) c.841G>A (p.Glu281Lys) c.2830G>A (p.Glu944Lys) c.1114G>A (p.Glu372Lys) | dbSNP |
2 | g.29197655C>A | CA346466400 | ALK,CLIP4 | c.*649C>A (n.*649C>A) c.3960G>T (p.Trp1320Cys) c.1187G>T n.837G>T c.756G>T (p.Trp252Cys) c.840G>T (p.Trp280Cys) c.2829G>T (p.Trp943Cys) c.1113G>T (p.Trp371Cys) | dbSNP |
2 | g.29197655C>G | CA346466415 | ALK,CLIP4 | c.*649C>G (n.*649C>G) c.3960G>C (p.Trp1320Cys) c.1187G>C n.837G>C c.756G>C (p.Trp252Cys) c.840G>C (p.Trp280Cys) c.2829G>C (p.Trp943Cys) c.1113G>C (p.Trp371Cys) | dbSNP |
2 | g.29197655C>T | CA346466421 | ALK,CLIP4 | c.*649C>T (n.*649C>T) c.3960G>A (p.Trp1320Ter) c.1187G>A n.837G>A c.756G>A (p.Trp252Ter) c.840G>A (p.Trp280Ter) c.2829G>A (p.Trp943Ter) c.1113G>A (p.Trp371Ter) | dbSNP |
2 | g.29197656C>A | CA346466424 | ALK,CLIP4 | c.*650C>A (n.*650C>A) c.3959G>T (p.Trp1320Leu) c.1186G>T n.836G>T c.755G>T (p.Trp252Leu) c.839G>T (p.Trp280Leu) c.2828G>T (p.Trp943Leu) c.1112G>T (p.Trp371Leu) | dbSNP |
2 | g.29197656C>G | CA346466431 | ALK,CLIP4 | c.*650C>G (n.*650C>G) c.3959G>C (p.Trp1320Ser) c.1186G>C n.836G>C c.755G>C (p.Trp252Ser) c.839G>C (p.Trp280Ser) c.2828G>C (p.Trp943Ser) c.1112G>C (p.Trp371Ser) | dbSNP |
2 | g.29197656C>T | CA346466433 | ALK,CLIP4 | c.*650C>T (n.*650C>T) c.3959G>A (p.Trp1320Ter) c.1186G>A n.836G>A c.755G>A (p.Trp252Ter) c.839G>A (p.Trp280Ter) c.2828G>A (p.Trp943Ter) c.1112G>A (p.Trp371Ter) | ClinVar dbSNP |
2 | g.29197657A= | CA1241075464 | ALK,CLIP4 | c.*651A= (n.*651A=) c.3958T= (p.Trp1320=) c.1185T= n.835T= c.754T= (p.Trp252=) c.838T= (p.Trp280=) c.2827T= (p.Trp943=) c.1111T= (p.Trp371=) | |
2 | g.29197657A>C | CA346466436 | ALK,CLIP4 | c.*651A>C (n.*651A>C) c.3958T>G (p.Trp1320Gly) c.1185T>G n.835T>G c.754T>G (p.Trp252Gly) c.838T>G (p.Trp280Gly) c.2827T>G (p.Trp943Gly) c.1111T>G (p.Trp371Gly) | dbSNP |
2 | g.29197657A>G | CA1593707 | ALK,CLIP4 | c.*651A>G (n.*651A>G) c.3958T>C (p.Trp1320Arg) c.1185T>C n.835T>C c.754T>C (p.Trp252Arg) c.838T>C (p.Trp280Arg) c.2827T>C (p.Trp943Arg) c.1111T>C (p.Trp371Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197657A>T | CA346466439 | ALK,CLIP4 | c.*651A>T (n.*651A>T) c.3958T>A (p.Trp1320Arg) c.1185T>A n.835T>A c.754T>A (p.Trp252Arg) c.838T>A (p.Trp280Arg) c.2827T>A (p.Trp943Arg) c.1111T>A (p.Trp371Arg) | dbSNP gnomAD v4 |
2 | g.29197658T>A | CA425433942 | ALK,CLIP4 | c.*652T>A (n.*652T>A) c.3957A>T (p.Leu1319=) c.1184A>T n.834A>T c.753A>T (p.Leu251=) c.837A>T (p.Leu279=) c.2826A>T (p.Leu942=) c.1110A>T (p.Leu370=) | dbSNP |
2 | g.29197658T>C | CA1593708 | ALK,CLIP4 | c.*652T>C (n.*652T>C) c.3957A>G (p.Leu1319=) c.1184A>G n.834A>G c.753A>G (p.Leu251=) c.837A>G (p.Leu279=) c.2826A>G (p.Leu942=) c.1110A>G (p.Leu370=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29197658T>G | CA425433943 | ALK,CLIP4 | c.*652T>G (n.*652T>G) c.3957A>C (p.Leu1319=) c.1184A>C n.834A>C c.753A>C (p.Leu251=) c.837A>C (p.Leu279=) c.2826A>C (p.Leu942=) c.1110A>C (p.Leu370=) | ClinVar |
2 | g.29197658T= | CA1241075470 | ALK,CLIP4 | c.*652T= (n.*652T=) c.3957A= (p.Leu1319=) c.1184A= n.834A= c.753A= (p.Leu251=) c.837A= (p.Leu279=) c.2826A= (p.Leu942=) c.1110A= (p.Leu370=) | |
2 | g.29197659A>C | CA346466445 | ALK,CLIP4 | c.*653A>C (n.*653A>C) c.3956T>G (p.Leu1319Arg) c.1183T>G n.833T>G c.752T>G (p.Leu251Arg) c.836T>G (p.Leu279Arg) c.2825T>G (p.Leu942Arg) c.1109T>G (p.Leu370Arg) | |
2 | g.29197659A>G | CA346466446 | ALK,CLIP4 | c.*653A>G (n.*653A>G) c.3956T>C (p.Leu1319Pro) c.1183T>C n.833T>C c.752T>C (p.Leu251Pro) c.836T>C (p.Leu279Pro) c.2825T>C (p.Leu942Pro) c.1109T>C (p.Leu370Pro) | |
2 | g.29197659A>T | CA346466448 | ALK,CLIP4 | c.*653A>T (n.*653A>T) c.3956T>A (p.Leu1319Gln) c.1183T>A n.833T>A c.752T>A (p.Leu251Gln) c.836T>A (p.Leu279Gln) c.2825T>A (p.Leu942Gln) c.1109T>A (p.Leu370Gln) | |
2 | g.29197663_29197665del | CA2739292152 | ALK,CLIP4 | c.*657_*659del (n.*657_*659del) c.3954_3956del (p.Leu1319del) c.1181_1183del n.831_833del c.750_752del (p.Leu251del) c.834_836del (p.Leu279del) c.2823_2825del (p.Leu942del) c.1107_1109del (p.Leu370del) | |
2 | g.29197660G>A | CA425433944 | ALK,CLIP4 | c.*654G>A (n.*654G>A) c.3955C>T (p.Leu1319=) c.1182C>T n.832C>T c.751C>T (p.Leu251=) c.835C>T (p.Leu279=) c.2824C>T (p.Leu942=) c.1108C>T (p.Leu370=) | dbSNP |
2 | g.29197660G>C | CA346466452 | ALK,CLIP4 | c.*654G>C (n.*654G>C) c.3955C>G (p.Leu1319Val) c.1182C>G n.832C>G c.751C>G (p.Leu251Val) c.835C>G (p.Leu279Val) c.2824C>G (p.Leu942Val) c.1108C>G (p.Leu370Val) | dbSNP |
2 | g.29197660G>T | CA346466454 | ALK,CLIP4 | c.*654G>T (n.*654G>T) c.3955C>A (p.Leu1319Ile) c.1182C>A n.832C>A c.751C>A (p.Leu251Ile) c.835C>A (p.Leu279Ile) c.2824C>A (p.Leu942Ile) c.1108C>A (p.Leu370Ile) | |
2 | g.29197661C>A | CA425433945 | ALK,CLIP4 | c.*655C>A (n.*655C>A) c.3954G>T (p.Leu1318=) c.1181G>T n.831G>T c.750G>T (p.Leu250=) c.834G>T (p.Leu278=) c.2823G>T (p.Leu941=) c.1107G>T (p.Leu369=) | dbSNP |
2 | g.29197661C>G | CA425433946 | ALK,CLIP4 | c.*655C>G (n.*655C>G) c.3954G>C (p.Leu1318=) c.1181G>C n.831G>C c.750G>C (p.Leu250=) c.834G>C (p.Leu278=) c.2823G>C (p.Leu941=) c.1107G>C (p.Leu369=) | ClinVar dbSNP |
2 | g.29197661C>T | CA425433947 | ALK,CLIP4 | c.*655C>T (n.*655C>T) c.3954G>A (p.Leu1318=) c.1181G>A n.831G>A c.750G>A (p.Leu250=) c.834G>A (p.Leu278=) c.2823G>A (p.Leu941=) c.1107G>A (p.Leu369=) | dbSNP |
2 | g.29197662A>C | CA346466455 | ALK,CLIP4 | c.*656A>C (n.*656A>C) c.3953T>G (p.Leu1318Arg) c.1180T>G n.830T>G c.749T>G (p.Leu250Arg) c.833T>G (p.Leu278Arg) c.2822T>G (p.Leu941Arg) c.1106T>G (p.Leu369Arg) | |
2 | g.29197662A>G | CA346466457 | ALK,CLIP4 | c.*656A>G (n.*656A>G) c.3953T>C (p.Leu1318Pro) c.1180T>C n.830T>C c.749T>C (p.Leu250Pro) c.833T>C (p.Leu278Pro) c.2822T>C (p.Leu941Pro) c.1106T>C (p.Leu369Pro) | ClinVar dbSNP |
2 | g.29197662A>T | CA346466460 | ALK,CLIP4 | c.*656A>T (n.*656A>T) c.3953T>A (p.Leu1318Gln) c.1180T>A n.830T>A c.749T>A (p.Leu250Gln) c.833T>A (p.Leu278Gln) c.2822T>A (p.Leu941Gln) c.1106T>A (p.Leu369Gln) | dbSNP |
2 | g.29197663G>A | CA425433948 | ALK,CLIP4 | c.*657G>A (n.*657G>A) c.3952C>T (p.Leu1318=) c.1179C>T n.829C>T c.748C>T (p.Leu250=) c.832C>T (p.Leu278=) c.2821C>T (p.Leu941=) c.1105C>T (p.Leu369=) | dbSNP |
2 | g.29197663G>C | CA346466463 | ALK,CLIP4 | c.*657G>C (n.*657G>C) c.3952C>G (p.Leu1318Val) c.1179C>G n.829C>G c.748C>G (p.Leu250Val) c.832C>G (p.Leu278Val) c.2821C>G (p.Leu941Val) c.1105C>G (p.Leu369Val) | dbSNP |
2 | g.29197663G>T | CA346466464 | ALK,CLIP4 | c.*657G>T (n.*657G>T) c.3952C>A (p.Leu1318Met) c.1179C>A n.829C>A c.748C>A (p.Leu250Met) c.832C>A (p.Leu278Met) c.2821C>A (p.Leu941Met) c.1105C>A (p.Leu369Met) | dbSNP COSMIC |
2 | g.29197664C>A | CA425433950 | ALK,CLIP4 | c.*658C>A (n.*658C>A) c.3951G>T (p.Val1317=) c.1178G>T n.828G>T c.747G>T (p.Val249=) c.831G>T (p.Val277=) c.2820G>T (p.Val940=) c.1104G>T (p.Val368=) | dbSNP |
2 | g.29197664C>G | CA425433951 | ALK,CLIP4 | c.*658C>G (n.*658C>G) c.3951G>C (p.Val1317=) c.1178G>C n.828G>C c.747G>C (p.Val249=) c.831G>C (p.Val277=) c.2820G>C (p.Val940=) c.1104G>C (p.Val368=) | dbSNP |
2 | g.29197664C>T | CA425433949 | ALK,CLIP4 | c.*658C>T (n.*658C>T) c.3951G>A (p.Val1317=) c.1178G>A n.828G>A c.747G>A (p.Val249=) c.831G>A (p.Val277=) c.2820G>A (p.Val940=) c.1104G>A (p.Val368=) | ClinVar dbSNP gnomAD v4 |
2 | g.29197665A= | CA1241075472 | ALK,CLIP4 | c.*659A= (n.*659A=) c.3950T= (p.Val1317=) c.1177T= n.827T= c.746T= (p.Val249=) c.830T= (p.Val277=) c.2819T= (p.Val940=) c.1103T= (p.Val368=) | |
2 | g.29197665A>C | CA346466465 | ALK,CLIP4 | c.*659A>C (n.*659A>C) c.3950T>G (p.Val1317Gly) c.1177T>G n.827T>G c.746T>G (p.Val249Gly) c.830T>G (p.Val277Gly) c.2819T>G (p.Val940Gly) c.1103T>G (p.Val368Gly) | dbSNP |
2 | g.29197665A>G | CA346466466 | ALK,CLIP4 | c.*659A>G (n.*659A>G) c.3950T>C (p.Val1317Ala) c.1177T>C n.827T>C c.746T>C (p.Val249Ala) c.830T>C (p.Val277Ala) c.2819T>C (p.Val940Ala) c.1103T>C (p.Val368Ala) | |
2 | g.29197665A>T | CA346466467 | ALK,CLIP4 | c.*659A>T (n.*659A>T) c.3950T>A (p.Val1317Glu) c.1177T>A n.827T>A c.746T>A (p.Val249Glu) c.830T>A (p.Val277Glu) c.2819T>A (p.Val940Glu) c.1103T>A (p.Val368Glu) | dbSNP |
2 | g.29197666C>A | CA346466469 | ALK,CLIP4 | c.*660C>A (n.*660C>A) c.3949G>T (p.Val1317Leu) c.1176G>T n.826G>T c.745G>T (p.Val249Leu) c.829G>T (p.Val277Leu) c.2818G>T (p.Val940Leu) c.1102G>T (p.Val368Leu) | dbSNP |
2 | g.29197666C= | CA1241075477 | ALK,CLIP4 | c.*660C= (n.*660C=) c.3949G= (p.Val1317=) c.1176G= n.826G= c.745G= (p.Val249=) c.829G= (p.Val277=) c.2818G= (p.Val940=) c.1102G= (p.Val368=) | |
2 | g.29197666C>G | CA1593709 | ALK,CLIP4 | c.*660C>G (n.*660C>G) c.3949G>C (p.Val1317Leu) c.1176G>C n.826G>C c.745G>C (p.Val249Leu) c.829G>C (p.Val277Leu) c.2818G>C (p.Val940Leu) c.1102G>C (p.Val368Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29197666C>T | CA346466473 | ALK,CLIP4 | c.*660C>T (n.*660C>T) c.3949G>A (p.Val1317Met) c.1176G>A n.826G>A c.745G>A (p.Val249Met) c.829G>A (p.Val277Met) c.2818G>A (p.Val940Met) c.1102G>A (p.Val368Met) | ClinVar dbSNP |
2 | g.29197667T>A | CA425433952 | ALK,CLIP4 | c.*661T>A (n.*661T>A) c.3948A>T (p.Gly1316=) c.1175A>T n.825A>T c.744A>T (p.Gly248=) c.828A>T (p.Gly276=) c.2817A>T (p.Gly939=) c.1101A>T (p.Gly367=) | gnomAD v4 |
2 | g.29197667T>C | CA425433953 | ALK,CLIP4 | c.*661T>C (n.*661T>C) c.3948A>G (p.Gly1316=) c.1175A>G n.825A>G c.744A>G (p.Gly248=) c.828A>G (p.Gly276=) c.2817A>G (p.Gly939=) c.1101A>G (p.Gly367=) | ClinVar dbSNP |
2 | g.29197667T>G | CA425433954 | ALK,CLIP4 | c.*661T>G (n.*661T>G) c.3948A>C (p.Gly1316=) c.1175A>C n.825A>C c.744A>C (p.Gly248=) c.828A>C (p.Gly276=) c.2817A>C (p.Gly939=) c.1101A>C (p.Gly367=) | |
2 | g.29197668C>A | CA346466488 | ALK,CLIP4 | c.*662C>A (n.*662C>A) c.3947G>T (p.Gly1316Val) c.1174G>T n.824G>T c.743G>T (p.Gly248Val) c.827G>T (p.Gly276Val) c.2816G>T (p.Gly939Val) c.1100G>T (p.Gly367Val) | dbSNP |
2 | g.29197668C= | CA1241075481 | ALK,CLIP4 | c.*662C= (n.*662C=) c.3947G= (p.Gly1316=) c.1174G= n.824G= c.743G= (p.Gly248=) c.827G= (p.Gly276=) c.2816G= (p.Gly939=) c.1100G= (p.Gly367=) | |
2 | g.29197668C>G | CA346466489 | ALK,CLIP4 | c.*662C>G (n.*662C>G) c.3947G>C (p.Gly1316Ala) c.1174G>C n.824G>C c.743G>C (p.Gly248Ala) c.827G>C (p.Gly276Ala) c.2816G>C (p.Gly939Ala) c.1100G>C (p.Gly367Ala) | dbSNP |
2 | g.29197668C>T | CA346466490 | ALK,CLIP4 | c.*662C>T (n.*662C>T) c.3947G>A (p.Gly1316Glu) c.1174G>A n.824G>A c.743G>A (p.Gly248Glu) c.827G>A (p.Gly276Glu) c.2816G>A (p.Gly939Glu) c.1100G>A (p.Gly367Glu) | ClinVar dbSNP |
2 | g.29197669del | CA2698955014 | ALK,CLIP4 | c.*663del (n.*663del) c.3947del (p.Gly1316GlufsTer?) c.1174del n.824del c.743del (p.Gly248GlufsTer?) c.827del (p.Gly276GlufsTer?) c.2816del (p.Gly939GlufsTer?) c.1100del (p.Gly367GlufsTer?) | dbSNP |
2 | g.29197669C>A | CA346466493 | ALK,CLIP4 | c.*663C>A (n.*663C>A) c.3946G>T (p.Gly1316Ter) c.1173G>T n.823G>T c.742G>T (p.Gly248Ter) c.826G>T (p.Gly276Ter) c.2815G>T (p.Gly939Ter) c.1099G>T (p.Gly367Ter) | ClinVar dbSNP |
2 | g.29197669C>G | CA346466495 | ALK,CLIP4 | c.*663C>G (n.*663C>G) c.3946G>C (p.Gly1316Arg) c.1173G>C n.823G>C c.742G>C (p.Gly248Arg) c.826G>C (p.Gly276Arg) c.2815G>C (p.Gly939Arg) c.1099G>C (p.Gly367Arg) | dbSNP |
2 | g.29197669C>T | CA346466497 | ALK,CLIP4 | c.*663C>T (n.*663C>T) c.3946G>A (p.Gly1316Arg) c.1173G>A n.823G>A c.742G>A (p.Gly248Arg) c.826G>A (p.Gly276Arg) c.2815G>A (p.Gly939Arg) c.1099G>A (p.Gly367Arg) | dbSNP |
2 | g.29197670A= | CA1241075482 | ALK,CLIP4 | c.*664A= (n.*664A=) c.3945T= (p.Phe1315=) c.1172T= n.822T= c.741T= (p.Phe247=) c.825T= (p.Phe275=) c.2814T= (p.Phe938=) c.1098T= (p.Phe366=) | |
2 | g.29197670A>C | CA346466498 | ALK,CLIP4 | c.*664A>C (n.*664A>C) c.3945T>G (p.Phe1315Leu) c.1172T>G n.822T>G c.741T>G (p.Phe247Leu) c.825T>G (p.Phe275Leu) c.2814T>G (p.Phe938Leu) c.1098T>G (p.Phe366Leu) | dbSNP |
2 | g.29197670A>G | CA425433955 | ALK,CLIP4 | c.*664A>G (n.*664A>G) c.3945T>C (p.Phe1315=) c.1172T>C n.822T>C c.741T>C (p.Phe247=) c.825T>C (p.Phe275=) c.2814T>C (p.Phe938=) c.1098T>C (p.Phe366=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29197670A>T | CA346466499 | ALK,CLIP4 | c.*664A>T (n.*664A>T) c.3945T>A (p.Phe1315Leu) c.1172T>A n.822T>A c.741T>A (p.Phe247Leu) c.825T>A (p.Phe275Leu) c.2814T>A (p.Phe938Leu) c.1098T>A (p.Phe366Leu) | dbSNP |
2 | g.29197672dup | CA2582342359 | ALK,CLIP4 | c.*666dup (n.*666dup) c.3945dup (p.Gly1316TrpfsTer?) c.1172dup n.822dup c.741dup (p.Gly248TrpfsTer?) c.825dup (p.Gly276TrpfsTer?) c.2814dup (p.Gly939TrpfsTer?) c.1098dup (p.Gly367TrpfsTer?) | ClinVar |
2 | g.29197671A>C | CA346466502 | ALK,CLIP4 | c.*665A>C (n.*665A>C) c.3944T>G (p.Phe1315Cys) c.1171T>G n.821T>G c.740T>G (p.Phe247Cys) c.824T>G (p.Phe275Cys) c.2813T>G (p.Phe938Cys) c.1097T>G (p.Phe366Cys) | dbSNP gnomAD v4 |
2 | g.29197671A>G | CA346466506 | ALK,CLIP4 | c.*665A>G (n.*665A>G) c.3944T>C (p.Phe1315Ser) c.1171T>C n.821T>C c.740T>C (p.Phe247Ser) c.824T>C (p.Phe275Ser) c.2813T>C (p.Phe938Ser) c.1097T>C (p.Phe366Ser) | ClinVar dbSNP |
2 | g.29197671A>T | CA346466510 | ALK,CLIP4 | c.*665A>T (n.*665A>T) c.3944T>A (p.Phe1315Tyr) c.1171T>A n.821T>A c.740T>A (p.Phe247Tyr) c.824T>A (p.Phe275Tyr) c.2813T>A (p.Phe938Tyr) c.1097T>A (p.Phe366Tyr) | dbSNP |
2 | g.29197672A>C | CA346466520 | ALK,CLIP4 | c.*666A>C (n.*666A>C) c.3943T>G (p.Phe1315Val) c.1170T>G n.820T>G c.739T>G (p.Phe247Val) c.823T>G (p.Phe275Val) c.2812T>G (p.Phe938Val) c.1096T>G (p.Phe366Val) | |
2 | g.29197672A>G | CA346466517 | ALK,CLIP4 | c.*666A>G (n.*666A>G) c.3943T>C (p.Phe1315Leu) c.1170T>C n.820T>C c.739T>C (p.Phe247Leu) c.823T>C (p.Phe275Leu) c.2812T>C (p.Phe938Leu) c.1096T>C (p.Phe366Leu) | dbSNP |
2 | g.29197672A>T | CA346466512 | ALK,CLIP4 | c.*666A>T (n.*666A>T) c.3943T>A (p.Phe1315Ile) c.1170T>A n.820T>A c.739T>A (p.Phe247Ile) c.823T>A (p.Phe275Ile) c.2812T>A (p.Phe938Ile) c.1096T>A (p.Phe366Ile) | dbSNP |
2 | g.29197673G>A | CA425433956 | ALK,CLIP4 | c.*667G>A (n.*667G>A) c.3942C>T (p.Ser1314=) c.1169C>T n.819C>T c.738C>T (p.Ser246=) c.822C>T (p.Ser274=) c.2811C>T (p.Ser937=) c.1095C>T (p.Ser365=) | dbSNP COSMIC |
2 | g.29197673G>C | CA425433957 | ALK,CLIP4 | c.*667G>C (n.*667G>C) c.3942C>G (p.Ser1314=) c.1169C>G n.819C>G c.738C>G (p.Ser246=) c.822C>G (p.Ser274=) c.2811C>G (p.Ser937=) c.1095C>G (p.Ser365=) | ClinVar dbSNP |
2 | g.29197673G>T | CA425433958 | ALK,CLIP4 | c.*667G>T (n.*667G>T) c.3942C>A (p.Ser1314=) c.1169C>A n.819C>A c.738C>A (p.Ser246=) c.822C>A (p.Ser274=) c.2811C>A (p.Ser937=) c.1095C>A (p.Ser365=) | dbSNP |
2 | g.29197674G>A | CA346466525 | ALK,CLIP4 | c.*668G>A (n.*668G>A) c.3941C>T (p.Ser1314Phe) c.1168C>T n.818C>T c.737C>T (p.Ser246Phe) c.821C>T (p.Ser274Phe) c.2810C>T (p.Ser937Phe) c.1094C>T (p.Ser365Phe) | |
2 | g.29197674G>C | CA346466530 | ALK,CLIP4 | c.*668G>C (n.*668G>C) c.3941C>G (p.Ser1314Cys) c.1168C>G n.818C>G c.737C>G (p.Ser246Cys) c.821C>G (p.Ser274Cys) c.2810C>G (p.Ser937Cys) c.1094C>G (p.Ser365Cys) | ClinVar |
2 | g.29197674G>T | CA346466558 | ALK,CLIP4 | c.*668G>T (n.*668G>T) c.3941C>A (p.Ser1314Tyr) c.1168C>A n.818C>A c.737C>A (p.Ser246Tyr) c.821C>A (p.Ser274Tyr) c.2810C>A (p.Ser937Tyr) c.1094C>A (p.Ser365Tyr) | |
2 | g.29197675A>C | CA346466561 | ALK,CLIP4 | c.*669A>C (n.*669A>C) c.3940T>G (p.Ser1314Ala) c.1167T>G n.817T>G c.736T>G (p.Ser246Ala) c.820T>G (p.Ser274Ala) c.2809T>G (p.Ser937Ala) c.1093T>G (p.Ser365Ala) | dbSNP |
2 | g.29197675A>G | CA346466565 | ALK,CLIP4 | c.*669A>G (n.*669A>G) c.3940T>C (p.Ser1314Pro) c.1167T>C n.817T>C c.736T>C (p.Ser246Pro) c.820T>C (p.Ser274Pro) c.2809T>C (p.Ser937Pro) c.1093T>C (p.Ser365Pro) | dbSNP |
2 | g.29197675A>T | CA346466569 | ALK,CLIP4 | c.*669A>T (n.*669A>T) c.3940T>A (p.Ser1314Thr) c.1167T>A n.817T>A c.736T>A (p.Ser246Thr) c.820T>A (p.Ser274Thr) c.2809T>A (p.Ser937Thr) c.1093T>A (p.Ser365Thr) | dbSNP |
2 | g.29197676C>A | CA16610886 | ALK,CLIP4 | c.*670C>A (n.*670C>A) c.3939G>T (p.Trp1313Cys) c.1166G>T n.816G>T c.735G>T (p.Trp245Cys) c.819G>T (p.Trp273Cys) c.2808G>T (p.Trp936Cys) c.1092G>T (p.Trp364Cys) | ClinVar dbSNP |
2 | g.29197676C= | CA1241075486 | ALK,CLIP4 | c.*670C= (n.*670C=) c.3939G= (p.Trp1313=) c.1166G= n.816G= c.735G= (p.Trp245=) c.819G= (p.Trp273=) c.2808G= (p.Trp936=) c.1092G= (p.Trp364=) | |
2 | g.29197676C>G | CA346466576 | ALK,CLIP4 | c.*670C>G (n.*670C>G) c.3939G>C (p.Trp1313Cys) c.1166G>C n.816G>C c.735G>C (p.Trp245Cys) c.819G>C (p.Trp273Cys) c.2808G>C (p.Trp936Cys) c.1092G>C (p.Trp364Cys) | |
2 | g.29197676C>T | CA346466578 | ALK,CLIP4 | c.*670C>T (n.*670C>T) c.3939G>A (p.Trp1313Ter) c.1166G>A n.816G>A c.735G>A (p.Trp245Ter) c.819G>A (p.Trp273Ter) c.2808G>A (p.Trp936Ter) c.1092G>A (p.Trp364Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197677C>A | CA346466581 | ALK,CLIP4 | c.*671C>A (n.*671C>A) c.3939-1G>T (n.3939-1G>T) c.1166-1G>T n.816-1G>T c.735-1G>T (n.735-1G>T) c.819-1G>T (n.819-1G>T) c.2808-1G>T (n.2808-1G>T) c.1092-1G>T (n.1092-1G>T) | dbSNP |
2 | g.29197677C>G | CA346466583 | ALK,CLIP4 | c.*671C>G (n.*671C>G) c.3939-1G>C (n.3939-1G>C) c.1166-1G>C n.816-1G>C c.735-1G>C (n.735-1G>C) c.819-1G>C (n.819-1G>C) c.2808-1G>C (n.2808-1G>C) c.1092-1G>C (n.1092-1G>C) | dbSNP |
2 | g.29197677C>T | CA346466586 | ALK,CLIP4 | c.*671C>T (n.*671C>T) c.3939-1G>A (n.3939-1G>A) c.1166-1G>A n.816-1G>A c.735-1G>A (n.735-1G>A) c.819-1G>A (n.819-1G>A) c.2808-1G>A (n.2808-1G>A) c.1092-1G>A (n.1092-1G>A) | dbSNP |
2 | g.29197678T>A | CA346466596 | ALK,CLIP4 | c.*672T>A (n.*672T>A) c.3939-2A>T (n.3939-2A>T) c.1166-2A>T n.816-2A>T c.735-2A>T (n.735-2A>T) c.819-2A>T (n.819-2A>T) c.2808-2A>T (n.2808-2A>T) c.1092-2A>T (n.1092-2A>T) | dbSNP |
2 | g.29197678T>C | CA346466592 | ALK,CLIP4 | c.*672T>C (n.*672T>C) c.3939-2A>G (n.3939-2A>G) c.1166-2A>G n.816-2A>G c.735-2A>G (n.735-2A>G) c.819-2A>G (n.819-2A>G) c.2808-2A>G (n.2808-2A>G) c.1092-2A>G (n.1092-2A>G) | dbSNP |
2 | g.29197678T>G | CA346466590 | ALK,CLIP4 | c.*672T>G (n.*672T>G) c.3939-2A>C (n.3939-2A>C) c.1166-2A>C n.816-2A>C c.735-2A>C (n.735-2A>C) c.819-2A>C (n.819-2A>C) c.2808-2A>C (n.2808-2A>C) c.1092-2A>C (n.1092-2A>C) | |
2 | g.29197679G>A | CA2580611261 | ALK,CLIP4 | c.*673G>A (n.*673G>A) c.3939-3C>T (n.3939-3C>T) c.1166-3C>T n.816-3C>T c.735-3C>T (n.735-3C>T) c.819-3C>T (n.819-3C>T) c.2808-3C>T (n.2808-3C>T) c.1092-3C>T (n.1092-3C>T) | ClinVar dbSNP gnomAD v4 |
2 | g.29197679G>C | CA2698955118 | ALK,CLIP4 | c.*673G>C (n.*673G>C) c.3939-3C>G (n.3939-3C>G) c.1166-3C>G n.816-3C>G c.735-3C>G (n.735-3C>G) c.819-3C>G (n.819-3C>G) c.2808-3C>G (n.2808-3C>G) c.1092-3C>G (n.1092-3C>G) | dbSNP |
2 | g.29197679G>T | CA2698955117 | ALK,CLIP4 | c.*673G>T (n.*673G>T) c.3939-3C>A (n.3939-3C>A) c.1166-3C>A n.816-3C>A c.735-3C>A (n.735-3C>A) c.819-3C>A (n.819-3C>A) c.2808-3C>A (n.2808-3C>A) c.1092-3C>A (n.1092-3C>A) | dbSNP |
2 | g.29197680G>A | CA2698955121 | ALK,CLIP4 | c.*674G>A (n.*674G>A) c.3939-4C>T (n.3939-4C>T) c.1166-4C>T n.816-4C>T c.735-4C>T (n.735-4C>T) c.819-4C>T (n.819-4C>T) c.2808-4C>T (n.2808-4C>T) c.1092-4C>T (n.1092-4C>T) | ClinVar dbSNP |
2 | g.29197680G>C | CA2698955123 | ALK,CLIP4 | c.*674G>C (n.*674G>C) c.3939-4C>G (n.3939-4C>G) c.1166-4C>G n.816-4C>G c.735-4C>G (n.735-4C>G) c.819-4C>G (n.819-4C>G) c.2808-4C>G (n.2808-4C>G) c.1092-4C>G (n.1092-4C>G) | dbSNP |
2 | g.29197680G>T | CA2576925448 | ALK,CLIP4 | c.*674G>T (n.*674G>T) c.3939-4C>A (n.3939-4C>A) c.1166-4C>A n.816-4C>A c.735-4C>A (n.735-4C>A) c.819-4C>A (n.819-4C>A) c.2808-4C>A (n.2808-4C>A) c.1092-4C>A (n.1092-4C>A) | dbSNP |
2 | g.29197681G>A | CA915943707 | ALK,CLIP4 | c.*675G>A (n.*675G>A) c.3939-5C>T (n.3939-5C>T) c.1166-5C>T n.816-5C>T c.735-5C>T (n.735-5C>T) c.819-5C>T (n.819-5C>T) c.2808-5C>T (n.2808-5C>T) c.1092-5C>T (n.1092-5C>T) | ClinVar dbSNP gnomAD v4 |
2 | g.29197681G>C | CA2698809444 | ALK,CLIP4 | c.*675G>C (n.*675G>C) c.3939-5C>G (n.3939-5C>G) c.1166-5C>G n.816-5C>G c.735-5C>G (n.735-5C>G) c.819-5C>G (n.819-5C>G) c.2808-5C>G (n.2808-5C>G) c.1092-5C>G (n.1092-5C>G) | dbSNP |
2 | g.29197681G= | CA1241075491 | ALK,CLIP4 | c.*675G= (n.*675G=) c.3939-5C= (n.3939-5C=) c.1166-5C= n.816-5C= c.735-5C= (n.735-5C=) c.819-5C= (n.819-5C=) c.2808-5C= (n.2808-5C=) c.1092-5C= (n.1092-5C=) | |
2 | g.29197682C>A | CA2698955125 | ALK,CLIP4 | c.*676C>A (n.*676C>A) c.3939-6G>T (n.3939-6G>T) c.1166-6G>T n.816-6G>T c.735-6G>T (n.735-6G>T) c.819-6G>T (n.819-6G>T) c.2808-6G>T (n.2808-6G>T) c.1092-6G>T (n.1092-6G>T) | dbSNP |
2 | g.29197682C>G | CA2698955146 | ALK,CLIP4 | c.*676C>G (n.*676C>G) c.3939-6G>C (n.3939-6G>C) c.1166-6G>C n.816-6G>C c.735-6G>C (n.735-6G>C) c.819-6G>C (n.819-6G>C) c.2808-6G>C (n.2808-6G>C) c.1092-6G>C (n.1092-6G>C) | dbSNP |
2 | g.29197682C>T | CA2658458236 | ALK,CLIP4 | c.*676C>T (n.*676C>T) c.3939-6G>A (n.3939-6G>A) c.1166-6G>A n.816-6G>A c.735-6G>A (n.735-6G>A) c.819-6G>A (n.819-6G>A) c.2808-6G>A (n.2808-6G>A) c.1092-6G>A (n.1092-6G>A) | dbSNP gnomAD v4 |
2 | g.29197683A>C | CA2698955163 | ALK,CLIP4 | c.*677A>C (n.*677A>C) c.3939-7T>G (n.3939-7T>G) c.1166-7T>G n.816-7T>G c.735-7T>G (n.735-7T>G) c.819-7T>G (n.819-7T>G) c.2808-7T>G (n.2808-7T>G) c.1092-7T>G (n.1092-7T>G) | dbSNP |
2 | g.29197683A>G | CA2658458237 | ALK,CLIP4 | c.*677A>G (n.*677A>G) c.3939-7T>C (n.3939-7T>C) c.1166-7T>C n.816-7T>C c.735-7T>C (n.735-7T>C) c.819-7T>C (n.819-7T>C) c.2808-7T>C (n.2808-7T>C) c.1092-7T>C (n.1092-7T>C) | ClinVar gnomAD v4 |
2 | g.29197684T>C | CA1593710 | ALK,CLIP4 | c.*678T>C (n.*678T>C) c.3939-8A>G (n.3939-8A>G) c.1166-8A>G n.816-8A>G c.735-8A>G (n.735-8A>G) c.819-8A>G (n.819-8A>G) c.2808-8A>G (n.2808-8A>G) c.1092-8A>G (n.1092-8A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197684T>G | CA2499215867 | ALK,CLIP4 | c.*678T>G (n.*678T>G) c.3939-8A>C (n.3939-8A>C) c.1166-8A>C n.816-8A>C c.735-8A>C (n.735-8A>C) c.819-8A>C (n.819-8A>C) c.2808-8A>C (n.2808-8A>C) c.1092-8A>C (n.1092-8A>C) | ClinVar dbSNP |
2 | g.29197684T= | CA1241075496 | ALK,CLIP4 | c.*678T= (n.*678T=) c.3939-8A= (n.3939-8A=) c.1166-8A= n.816-8A= c.735-8A= (n.735-8A=) c.819-8A= (n.819-8A=) c.2808-8A= (n.2808-8A=) c.1092-8A= (n.1092-8A=) | |
2 | g.29197685G>A | CA1593711 | ALK,CLIP4 | c.*679G>A (n.*679G>A) c.3939-9C>T (n.3939-9C>T) c.1166-9C>T n.816-9C>T c.735-9C>T (n.735-9C>T) c.819-9C>T (n.819-9C>T) c.2808-9C>T (n.2808-9C>T) c.1092-9C>T (n.1092-9C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197685G>C | CA2698771051 | ALK,CLIP4 | c.*679G>C (n.*679G>C) c.3939-9C>G (n.3939-9C>G) c.1166-9C>G n.816-9C>G c.735-9C>G (n.735-9C>G) c.819-9C>G (n.819-9C>G) c.2808-9C>G (n.2808-9C>G) c.1092-9C>G (n.1092-9C>G) | dbSNP |
2 | g.29197685G= | CA1241075499 | ALK,CLIP4 | c.*679G= (n.*679G=) c.3939-9C= (n.3939-9C=) c.1166-9C= n.816-9C= c.735-9C= (n.735-9C=) c.819-9C= (n.819-9C=) c.2808-9C= (n.2808-9C=) c.1092-9C= (n.1092-9C=) | |
2 | g.29197685G>T | CA2698771052 | ALK,CLIP4 | c.*679G>T (n.*679G>T) c.3939-9C>A (n.3939-9C>A) c.1166-9C>A n.816-9C>A c.735-9C>A (n.735-9C>A) c.819-9C>A (n.819-9C>A) c.2808-9C>A (n.2808-9C>A) c.1092-9C>A (n.1092-9C>A) | dbSNP |
2 | g.29197686G>A | CA2698955167 | ALK,CLIP4 | c.*680G>A (n.*680G>A) c.3939-10C>T (n.3939-10C>T) c.1166-10C>T n.816-10C>T c.735-10C>T (n.735-10C>T) c.819-10C>T (n.819-10C>T) c.2808-10C>T (n.2808-10C>T) c.1092-10C>T (n.1092-10C>T) | dbSNP |
2 | g.29197686G>C | CA2573134633 | ALK,CLIP4 | c.*680G>C (n.*680G>C) c.3939-10C>G (n.3939-10C>G) c.1166-10C>G n.816-10C>G c.735-10C>G (n.735-10C>G) c.819-10C>G (n.819-10C>G) c.2808-10C>G (n.2808-10C>G) c.1092-10C>G (n.1092-10C>G) | ClinVar dbSNP |
2 | g.29197686G>T | CA2698955166 | ALK,CLIP4 | c.*680G>T (n.*680G>T) c.3939-10C>A (n.3939-10C>A) c.1166-10C>A n.816-10C>A c.735-10C>A (n.735-10C>A) c.819-10C>A (n.819-10C>A) c.2808-10C>A (n.2808-10C>A) c.1092-10C>A (n.1092-10C>A) | dbSNP |
2 | g.29197687G>A | CA2658458239 | ALK,CLIP4 | c.*681G>A (n.*681G>A) c.3939-11C>T (n.3939-11C>T) c.1166-11C>T n.816-11C>T c.735-11C>T (n.735-11C>T) c.819-11C>T (n.819-11C>T) c.2808-11C>T (n.2808-11C>T) c.1092-11C>T (n.1092-11C>T) | dbSNP gnomAD v4 |
2 | g.29197687G>C | CA1593712 | ALK,CLIP4 | c.*681G>C (n.*681G>C) c.3939-11C>G (n.3939-11C>G) c.1166-11C>G n.816-11C>G c.735-11C>G (n.735-11C>G) c.819-11C>G (n.819-11C>G) c.2808-11C>G (n.2808-11C>G) c.1092-11C>G (n.1092-11C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29197687G= | CA1241075503 | ALK,CLIP4 | c.*681G= (n.*681G=) c.3939-11C= (n.3939-11C=) c.1166-11C= n.816-11C= c.735-11C= (n.735-11C=) c.819-11C= (n.819-11C=) c.2808-11C= (n.2808-11C=) c.1092-11C= (n.1092-11C=) | |
2 | g.29197688A>C | CA2698955171 | ALK,CLIP4 | c.*682A>C (n.*682A>C) c.3939-12T>G (n.3939-12T>G) c.1166-12T>G n.816-12T>G c.735-12T>G (n.735-12T>G) c.819-12T>G (n.819-12T>G) c.2808-12T>G (n.2808-12T>G) c.1092-12T>G (n.1092-12T>G) | dbSNP |
2 | g.29197688A>G | CA2698955190 | ALK,CLIP4 | c.*682A>G (n.*682A>G) c.3939-12T>C (n.3939-12T>C) c.1166-12T>C n.816-12T>C c.735-12T>C (n.735-12T>C) c.819-12T>C (n.819-12T>C) c.2808-12T>C (n.2808-12T>C) c.1092-12T>C (n.1092-12T>C) | dbSNP |
2 | g.29197688A>T | CA2698955189 | ALK,CLIP4 | c.*682A>T (n.*682A>T) c.3939-12T>A (n.3939-12T>A) c.1166-12T>A n.816-12T>A c.735-12T>A (n.735-12T>A) c.819-12T>A (n.819-12T>A) c.2808-12T>A (n.2808-12T>A) c.1092-12T>A (n.1092-12T>A) | dbSNP |