| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.25209894G>A | CA2581077155 | KRAS | c.129C>T (p.Phe43=) c.468C>T (p.Phe156=) c.*439C>T (n.*439C>T) c.*166C>T (n.*166C>T) n.942C>T c.271C>T c.*429C>T (n.*429C>T) c.270C>T (p.Phe90=) c.393C>T (p.Phe131=) c.*22C>T (n.*22C>T) | |
| 12 | g.25209894G>C | CA279964 | KRAS | c.129C>G (p.Phe43Leu) c.468C>G (p.Phe156Leu) c.*439C>G (n.*439C>G) c.*166C>G (n.*166C>G) n.942C>G c.271C>G c.*429C>G (n.*429C>G) c.270C>G (p.Phe90Leu) c.393C>G (p.Phe131Leu) c.*22C>G (n.*22C>G) | ClinVar dbSNP COSMIC |
| 12 | g.25209894G= | CA2022884701 | KRAS | c.129C= (p.Phe43=) c.468C= (p.Phe156=) c.*439C= (n.*439C=) c.*166C= (n.*166C=) n.942C= c.271C= c.*429C= (n.*429C=) c.270C= (p.Phe90=) c.393C= (p.Phe131=) c.*22C= (n.*22C=) | |
| 12 | g.25209894G>T | CA384148507 | KRAS | c.129C>A (p.Phe43Leu) c.468C>A (p.Phe156Leu) c.*439C>A (n.*439C>A) c.*166C>A (n.*166C>A) n.942C>A c.271C>A c.*429C>A (n.*429C>A) c.270C>A (p.Phe90Leu) c.393C>A (p.Phe131Leu) c.*22C>A (n.*22C>A) | |
| 12 | g.25209895A>C | CA384148510 | KRAS | c.128T>G (p.Phe43Cys) c.467T>G (p.Phe156Cys) c.*438T>G (n.*438T>G) c.*165T>G (n.*165T>G) n.941T>G c.270T>G c.*428T>G (n.*428T>G) c.269T>G (p.Phe90Cys) c.392T>G (p.Phe131Cys) c.*21T>G (n.*21T>G) | |
| 12 | g.25209895A>G | CA384148508 | KRAS | c.128T>C (p.Phe43Ser) c.467T>C (p.Phe156Ser) c.*438T>C (n.*438T>C) c.*165T>C (n.*165T>C) n.941T>C c.270T>C c.*428T>C (n.*428T>C) c.269T>C (p.Phe90Ser) c.392T>C (p.Phe131Ser) c.*21T>C (n.*21T>C) | ClinVar |
| 12 | g.25209895A>T | CA384148509 | KRAS | c.128T>A (p.Phe43Tyr) c.467T>A (p.Phe156Tyr) c.*438T>A (n.*438T>A) c.*165T>A (n.*165T>A) n.941T>A c.270T>A c.*428T>A (n.*428T>A) c.269T>A (p.Phe90Tyr) c.392T>A (p.Phe131Tyr) c.*21T>A (n.*21T>A) | |
| 12 | g.25209896A= | CA2022884707 | KRAS | c.127T= (p.Phe43=) c.466T= (p.Phe156=) c.*437T= (n.*437T=) c.*164T= (n.*164T=) n.940T= c.269T= c.*427T= (n.*427T=) c.268T= (p.Phe90=) c.391T= (p.Phe131=) c.*20T= (n.*20T=) | |
| 12 | g.25209896A>C | CA261709 | KRAS | c.127T>G (p.Phe43Val) c.466T>G (p.Phe156Val) c.*437T>G (n.*437T>G) c.*164T>G (n.*164T>G) n.940T>G c.269T>G c.*427T>G (n.*427T>G) c.268T>G (p.Phe90Val) c.391T>G (p.Phe131Val) c.*20T>G (n.*20T>G) | ClinVar dbSNP |
| 12 | g.25209896A>G | CA384148511 | KRAS | c.127T>C (p.Phe43Leu) c.466T>C (p.Phe156Leu) c.*437T>C (n.*437T>C) c.*164T>C (n.*164T>C) n.940T>C c.269T>C c.*427T>C (n.*427T>C) c.268T>C (p.Phe90Leu) c.391T>C (p.Phe131Leu) c.*20T>C (n.*20T>C) | COSMIC |
| 12 | g.25209896A>T | CA273160 | KRAS | c.127T>A (p.Phe43Ile) c.466T>A (p.Phe156Ile) c.*437T>A (n.*437T>A) c.*164T>A (n.*164T>A) n.940T>A c.269T>A c.*427T>A (n.*427T>A) c.268T>A (p.Phe90Ile) c.391T>A (p.Phe131Ile) c.*20T>A (n.*20T>A) | ClinVar dbSNP |
| 12 | g.25209897G>C | CA2697559136 | KRAS | c.126C>G (p.Ala42=) c.465C>G (p.Ala155=) c.*436C>G (n.*436C>G) c.*163C>G (n.*163C>G) n.939C>G c.268C>G c.*426C>G (n.*426C>G) c.267C>G (p.Ala89=) c.390C>G (p.Ala130=) c.*19C>G (n.*19C>G) | ClinVar |
| 12 | g.25209897G>T | CA2978503551 | KRAS | c.126C>A (p.Ala42=) c.465C>A (p.Ala155=) c.*436C>A (n.*436C>A) c.*163C>A (n.*163C>A) n.939C>A c.268C>A c.*426C>A (n.*426C>A) c.267C>A (p.Ala89=) c.390C>A (p.Ala130=) c.*19C>A (n.*19C>A) | |
| 12 | g.25209898G>A | CA384148513 | KRAS | c.125C>T (p.Ala42Val) c.464C>T (p.Ala155Val) c.*435C>T (n.*435C>T) c.*162C>T (n.*162C>T) n.938C>T c.267C>T c.*425C>T (n.*425C>T) c.266C>T (p.Ala89Val) c.389C>T (p.Ala130Val) c.*18C>T (n.*18C>T) | |
| 12 | g.25209898G>C | CA6486828 | KRAS | c.125C>G (p.Ala42Gly) c.464C>G (p.Ala155Gly) c.*435C>G (n.*435C>G) c.*162C>G (n.*162C>G) n.938C>G c.267C>G c.*425C>G (n.*425C>G) c.266C>G (p.Ala89Gly) c.389C>G (p.Ala130Gly) c.*18C>G (n.*18C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.25209898G= | CA2022884713 | KRAS | c.125C= (p.Ala42=) c.464C= (p.Ala155=) c.*435C= (n.*435C=) c.*162C= (n.*162C=) n.938C= c.267C= c.*425C= (n.*425C=) c.266C= (p.Ala89=) c.389C= (p.Ala130=) c.*18C= (n.*18C=) | |
| 12 | g.25209898G>T | CA384148512 | KRAS | c.125C>A (p.Ala42Asp) c.464C>A (p.Ala155Asp) c.*435C>A (n.*435C>A) c.*162C>A (n.*162C>A) n.938C>A c.267C>A c.*425C>A (n.*425C>A) c.266C>A (p.Ala89Asp) c.389C>A (p.Ala130Asp) c.*18C>A (n.*18C>A) | |
| 12 | g.25209899C>A | CA384148514 | KRAS | c.124G>T (p.Ala42Ser) c.463G>T (p.Ala155Ser) c.*434G>T (n.*434G>T) c.*161G>T (n.*161G>T) n.937G>T c.266G>T c.*424G>T (n.*424G>T) c.265G>T (p.Ala89Ser) c.388G>T (p.Ala130Ser) c.*17G>T (n.*17G>T) | |
| 12 | g.25209899C>G | CA384148515 | KRAS | c.124G>C (p.Ala42Pro) c.463G>C (p.Ala155Pro) c.*434G>C (n.*434G>C) c.*161G>C (n.*161G>C) n.937G>C c.266G>C c.*424G>C (n.*424G>C) c.265G>C (p.Ala89Pro) c.388G>C (p.Ala130Pro) c.*17G>C (n.*17G>C) | |
| 12 | g.25209899C>T | CA384148516 | KRAS | c.124G>A (p.Ala42Thr) c.463G>A (p.Ala155Thr) c.*434G>A (n.*434G>A) c.*161G>A (n.*161G>A) n.937G>A c.266G>A c.*424G>A (n.*424G>A) c.265G>A (p.Ala89Thr) c.388G>A (p.Ala130Thr) c.*17G>A (n.*17G>A) | |
| 12 | g.25209904_25209906del | CA645572083 | KRAS | c.122_124del (p.Asp41del) c.461_463del (p.Asp154del) c.*432_*434del (n.*432_*434del) c.*159_*161del (n.*159_*161del) n.935_937del c.264_266del c.*422_*424del (n.*422_*424del) c.263_265del (p.Asp88del) c.386_388del (p.Asp129del) c.*15_*17del (n.*15_*17del) | gnomAD v4 COSMIC |
| 12 | g.25209900A= | CA2022884716 | KRAS | c.123T= (p.Asp41=) c.462T= (p.Asp154=) c.*433T= (n.*433T=) c.*160T= (n.*160T=) n.936T= c.265T= c.*423T= (n.*423T=) c.264T= (p.Asp88=) c.387T= (p.Asp129=) c.*16T= (n.*16T=) | |
| 12 | g.25209900A>C | CA384148517 | KRAS | c.123T>G (p.Asp41Glu) c.462T>G (p.Asp154Glu) c.*433T>G (n.*433T>G) c.*160T>G (n.*160T>G) n.936T>G c.265T>G c.*423T>G (n.*423T>G) c.264T>G (p.Asp88Glu) c.387T>G (p.Asp129Glu) c.*16T>G (n.*16T>G) | |
| 12 | g.25209900A>G | CA6486829 | KRAS | c.123T>C (p.Asp41=) c.462T>C (p.Asp154=) c.*433T>C (n.*433T>C) c.*160T>C (n.*160T>C) n.936T>C c.265T>C c.*423T>C (n.*423T>C) c.264T>C (p.Asp88=) c.387T>C (p.Asp129=) c.*16T>C (n.*16T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.25209900A>T | CA384148518 | KRAS | c.123T>A (p.Asp41Glu) c.462T>A (p.Asp154Glu) c.*433T>A (n.*433T>A) c.*160T>A (n.*160T>A) n.936T>A c.265T>A c.*423T>A (n.*423T>A) c.264T>A (p.Asp88Glu) c.387T>A (p.Asp129Glu) c.*16T>A (n.*16T>A) | |
| 12 | g.25209901T>A | CA384148519 | KRAS | c.122A>T (p.Asp41Val) c.461A>T (p.Asp154Val) c.*432A>T (n.*432A>T) c.*159A>T (n.*159A>T) n.935A>T c.264A>T c.*422A>T (n.*422A>T) c.263A>T (p.Asp88Val) c.386A>T (p.Asp129Val) c.*15A>T (n.*15A>T) | |
| 12 | g.25209901T>C | CA384148521 | KRAS | c.122A>G (p.Asp41Gly) c.461A>G (p.Asp154Gly) c.*432A>G (n.*432A>G) c.*159A>G (n.*159A>G) n.935A>G c.264A>G c.*422A>G (n.*422A>G) c.263A>G (p.Asp88Gly) c.386A>G (p.Asp129Gly) c.*15A>G (n.*15A>G) | ClinVar dbSNP |
| 12 | g.25209901T>G | CA384148520 | KRAS | c.122A>C (p.Asp41Ala) c.461A>C (p.Asp154Ala) c.*432A>C (n.*432A>C) c.*159A>C (n.*159A>C) n.935A>C c.264A>C c.*422A>C (n.*422A>C) c.263A>C (p.Asp88Ala) c.386A>C (p.Asp129Ala) c.*15A>C (n.*15A>C) | |
| 12 | g.25209902C>A | CA384148522 | KRAS | c.121G>T (p.Asp41Tyr) c.460G>T (p.Asp154Tyr) c.*431G>T (n.*431G>T) c.*158G>T (n.*158G>T) n.934G>T c.263G>T c.*421G>T (n.*421G>T) c.262G>T (p.Asp88Tyr) c.385G>T (p.Asp129Tyr) c.*14G>T (n.*14G>T) | |
| 12 | g.25209902C>G | CA384148523 | KRAS | c.121G>C (p.Asp41His) c.460G>C (p.Asp154His) c.*431G>C (n.*431G>C) c.*158G>C (n.*158G>C) n.934G>C c.263G>C c.*421G>C (n.*421G>C) c.262G>C (p.Asp88His) c.385G>C (p.Asp129His) c.*14G>C (n.*14G>C) | |
| 12 | g.25209902C>T | CA384148524 | KRAS | c.121G>A (p.Asp41Asn) c.460G>A (p.Asp154Asn) c.*431G>A (n.*431G>A) c.*158G>A (n.*158G>A) n.934G>A c.263G>A c.*421G>A (n.*421G>A) c.262G>A (p.Asp88Asn) c.385G>A (p.Asp129Asn) c.*14G>A (n.*14G>A) | |
| 12 | g.25209903A>C | CA384148525 | KRAS | c.120T>G (p.Asp40Glu) c.459T>G (p.Asp153Glu) c.*430T>G (n.*430T>G) c.*157T>G (n.*157T>G) n.933T>G c.262T>G c.*420T>G (n.*420T>G) c.261T>G (p.Asp87Glu) c.384T>G (p.Asp128Glu) c.*13T>G (n.*13T>G) | |
| 12 | g.25209903A>G | CA2794888727 | KRAS | c.120T>C (p.Asp40=) c.459T>C (p.Asp153=) c.*430T>C (n.*430T>C) c.*157T>C (n.*157T>C) n.933T>C c.262T>C c.*420T>C (n.*420T>C) c.261T>C (p.Asp87=) c.384T>C (p.Asp128=) c.*13T>C (n.*13T>C) | |
| 12 | g.25209903A>T | CA384148526 | KRAS | c.120T>A (p.Asp40Glu) c.459T>A (p.Asp153Glu) c.*430T>A (n.*430T>A) c.*157T>A (n.*157T>A) n.933T>A c.262T>A c.*420T>A (n.*420T>A) c.261T>A (p.Asp87Glu) c.384T>A (p.Asp128Glu) c.*13T>A (n.*13T>A) | |
| 12 | g.25209904T>A | CA256478 | KRAS | c.119A>T (p.Asp40Val) c.458A>T (p.Asp153Val) c.*429A>T (n.*429A>T) c.*156A>T (n.*156A>T) n.932A>T c.261A>T c.*419A>T (n.*419A>T) c.260A>T (p.Asp87Val) c.383A>T (p.Asp128Val) c.*12A>T (n.*12A>T) | ClinVar dbSNP COSMIC |
| 12 | g.25209904T>C | CA261707 | KRAS | c.119A>G (p.Asp40Gly) c.458A>G (p.Asp153Gly) c.*429A>G (n.*429A>G) c.*156A>G (n.*156A>G) n.932A>G c.261A>G c.*419A>G (n.*419A>G) c.260A>G (p.Asp87Gly) c.383A>G (p.Asp128Gly) c.*12A>G (n.*12A>G) | ClinVar dbSNP gnomAD v4 |
| 12 | g.25209904T>G | CA384148527 | KRAS | c.119A>C (p.Asp40Ala) c.458A>C (p.Asp153Ala) c.*429A>C (n.*429A>C) c.*156A>C (n.*156A>C) n.932A>C c.261A>C c.*419A>C (n.*419A>C) c.260A>C (p.Asp87Ala) c.383A>C (p.Asp128Ala) c.*12A>C (n.*12A>C) | |
| 12 | g.25209904T= | CA2022884725 | KRAS | c.119A= (p.Asp40=) c.458A= (p.Asp153=) c.*429A= (n.*429A=) c.*156A= (n.*156A=) n.932A= c.261A= c.*419A= (n.*419A=) c.260A= (p.Asp87=) c.383A= (p.Asp128=) c.*12A= (n.*12A=) | |
| 12 | g.25209905del | CA2575103843 | KRAS | c.118del (p.Asp40MetfsTer7) c.457del (p.Asp153MetfsTer7) c.*428del (n.*428del) c.*155del (n.*155del) n.931del c.260del c.*418del (n.*418del) c.259del (p.Asp87MetfsTer7) c.382del (p.Asp128MetfsTer7) c.*11del (n.*11del) | |
| 12 | g.25209905C>A | CA384148528 | KRAS | c.118G>T (p.Asp40Tyr) c.457G>T (p.Asp153Tyr) c.*428G>T (n.*428G>T) c.*155G>T (n.*155G>T) n.931G>T c.260G>T c.*418G>T (n.*418G>T) c.259G>T (p.Asp87Tyr) c.382G>T (p.Asp128Tyr) c.*11G>T (n.*11G>T) | dbSNP |
| 12 | g.25209905C= | CA2022884728 | KRAS | c.118G= (p.Asp40=) c.457G= (p.Asp153=) c.*428G= (n.*428G=) c.*155G= (n.*155G=) n.931G= c.260G= c.*418G= (n.*418G=) c.259G= (p.Asp87=) c.382G= (p.Asp128=) c.*11G= (n.*11G=) | |
| 12 | g.25209905C>G | CA384148529 | KRAS | c.118G>C (p.Asp40His) c.457G>C (p.Asp153His) c.*428G>C (n.*428G>C) c.*155G>C (n.*155G>C) n.931G>C c.260G>C c.*418G>C (n.*418G>C) c.259G>C (p.Asp87His) c.382G>C (p.Asp128His) c.*11G>C (n.*11G>C) | |
| 12 | g.25209905C>T | CA384148530 | KRAS | c.118G>A (p.Asp40Asn) c.457G>A (p.Asp153Asn) c.*428G>A (n.*428G>A) c.*155G>A (n.*155G>A) n.931G>A c.260G>A c.*418G>A (n.*418G>A) c.259G>A (p.Asp87Asn) c.382G>A (p.Asp128Asn) c.*11G>A (n.*11G>A) | ClinVar dbSNP COSMIC |
| 12 | g.25209906A= | CA2022884733 | KRAS | c.117T= (p.Val39=) c.456T= (p.Val152=) c.*427T= (n.*427T=) c.*154T= (n.*154T=) n.930T= c.259T= c.*417T= (n.*417T=) c.258T= (p.Val86=) c.381T= (p.Val127=) c.*10T= (n.*10T=) | |
| 12 | g.25209906A>C | CA6486830 | KRAS | c.117T>G (p.Val39=) c.456T>G (p.Val152=) c.*427T>G (n.*427T>G) c.*154T>G (n.*154T>G) n.930T>G c.259T>G c.*417T>G (n.*417T>G) c.258T>G (p.Val86=) c.381T>G (p.Val127=) c.*10T>G (n.*10T>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.25209906A>G | CA686714911 | KRAS | c.117T>C (p.Val39=) c.456T>C (p.Val152=) c.*427T>C (n.*427T>C) c.*154T>C (n.*154T>C) n.930T>C c.259T>C c.*417T>C (n.*417T>C) c.258T>C (p.Val86=) c.381T>C (p.Val127=) c.*10T>C (n.*10T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.25209907A= | CA2022884736 | KRAS | c.116T= (p.Val39=) c.455T= (p.Val152=) c.*426T= (n.*426T=) c.*153T= (n.*153T=) n.929T= c.258T= c.*416T= (n.*416T=) c.257T= (p.Val86=) c.380T= (p.Val127=) c.*9T= (n.*9T=) | |
| 12 | g.25209907A>C | CA256482 | KRAS | c.116T>G (p.Val39Gly) c.455T>G (p.Val152Gly) c.*426T>G (n.*426T>G) c.*153T>G (n.*153T>G) n.929T>G c.258T>G c.*416T>G (n.*416T>G) c.257T>G (p.Val86Gly) c.380T>G (p.Val127Gly) c.*9T>G (n.*9T>G) | ClinVar dbSNP |
| 12 | g.25209907A>G | CA384148531 | KRAS | c.116T>C (p.Val39Ala) c.455T>C (p.Val152Ala) c.*426T>C (n.*426T>C) c.*153T>C (n.*153T>C) n.929T>C c.258T>C c.*416T>C (n.*416T>C) c.257T>C (p.Val86Ala) c.380T>C (p.Val127Ala) c.*9T>C (n.*9T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.25209907A>T | CA384148532 | KRAS | c.116T>A (p.Val39Asp) c.455T>A (p.Val152Asp) c.*426T>A (n.*426T>A) c.*153T>A (n.*153T>A) n.929T>A c.258T>A c.*416T>A (n.*416T>A) c.257T>A (p.Val86Asp) c.380T>A (p.Val127Asp) c.*9T>A (n.*9T>A) |