Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.29226975A= | CA1241092854 | ALK | c.3014T= (p.Ile1005=) c.180T= c.1883T= (p.Ile628=) c.167T= (p.Ile56=) n.3870T= | |
2 | g.29226975A>C | CA346467637 | ALK | c.3014T>G (p.Ile1005Ser) c.180T>G c.1883T>G (p.Ile628Ser) c.167T>G (p.Ile56Ser) n.3870T>G | dbSNP |
2 | g.29226975A>G | CA346467638 | ALK | c.3014T>C (p.Ile1005Thr) c.180T>C c.1883T>C (p.Ile628Thr) c.167T>C (p.Ile56Thr) n.3870T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29226975A>T | CA346467639 | ALK | c.3014T>A (p.Ile1005Asn) c.180T>A c.1883T>A (p.Ile628Asn) c.167T>A (p.Ile56Asn) n.3870T>A | dbSNP |
2 | g.29226976T>A | CA346467640 | ALK | c.3013A>T (p.Ile1005Phe) c.179A>T c.1882A>T (p.Ile628Phe) c.166A>T (p.Ile56Phe) n.3869A>T | dbSNP |
2 | g.29226976T>C | CA346467641 | ALK | c.3013A>G (p.Ile1005Val) c.179A>G c.1882A>G (p.Ile628Val) c.166A>G (p.Ile56Val) n.3869A>G | ClinVar dbSNP gnomAD v4 |
2 | g.29226976T>G | CA346467642 | ALK | c.3013A>C (p.Ile1005Leu) c.179A>C c.1882A>C (p.Ile628Leu) c.166A>C (p.Ile56Leu) n.3869A>C | dbSNP |
2 | g.29226976T= | CA1241092855 | ALK | c.3013A= (p.Ile1005=) c.179A= c.1882A= (p.Ile628=) c.166A= (p.Ile56=) n.3869A= | |
2 | g.29226977G>A | CA425435958 | ALK | c.3012C>T (p.Val1004=) c.178C>T c.1881C>T (p.Val627=) c.165C>T (p.Val55=) n.3868C>T | dbSNP |
2 | g.29226977G>C | CA425435959 | ALK | c.3012C>G (p.Val1004=) c.178C>G c.1881C>G (p.Val627=) c.165C>G (p.Val55=) n.3868C>G | ClinVar dbSNP |
2 | g.29226977G= | CA1241092856 | ALK | c.3012C= (p.Val1004=) c.178C= c.1881C= (p.Val627=) c.165C= (p.Val55=) n.3868C= | |
2 | g.29226977G>T | CA425435960 | ALK | c.3012C>A (p.Val1004=) c.178C>A c.1881C>A (p.Val627=) c.165C>A (p.Val55=) n.3868C>A | |
2 | g.29226978A>C | CA346467643 | ALK | c.3011T>G (p.Val1004Gly) c.177T>G c.1880T>G (p.Val627Gly) c.164T>G (p.Val55Gly) n.3867T>G | |
2 | g.29226978A>G | CA346467645 | ALK | c.3011T>C (p.Val1004Ala) c.177T>C c.1880T>C (p.Val627Ala) c.164T>C (p.Val55Ala) n.3867T>C | ClinVar dbSNP |
2 | g.29226978A>T | CA346467644 | ALK | c.3011T>A (p.Val1004Asp) c.177T>A c.1880T>A (p.Val627Asp) c.164T>A (p.Val55Asp) n.3867T>A | |
2 | g.29226979C>A | CA346467646 | ALK | c.3010G>T (p.Val1004Phe) c.176G>T c.1879G>T (p.Val627Phe) c.163G>T (p.Val55Phe) n.3866G>T | dbSNP |
2 | g.29226979C>G | CA346467647 | ALK | c.3010G>C (p.Val1004Leu) c.176G>C c.1879G>C (p.Val627Leu) c.163G>C (p.Val55Leu) n.3866G>C | dbSNP |
2 | g.29226979C>T | CA346467648 | ALK | c.3010G>A (p.Val1004Ile) c.176G>A c.1879G>A (p.Val627Ile) c.163G>A (p.Val55Ile) n.3866G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29226980dup | CA2843288605 | ALK | c.3010dup (p.Val1004GlyfsTer6) c.176dup c.1879dup (p.Val627GlyfsTer6) c.163dup (p.Val55GlyfsTer6) n.3866dup | |
2 | g.29226980C>A | CA346467649 | ALK | c.3009G>T (p.Lys1003Asn) c.175G>T c.1878G>T (p.Lys626Asn) c.162G>T (p.Lys54Asn) n.3865G>T | |
2 | g.29226980C= | CA1241092857 | ALK | c.3009G= (p.Lys1003=) c.175G= c.1878G= (p.Lys626=) c.162G= (p.Lys54=) n.3865G= | |
2 | g.29226980C>G | CA346467650 | ALK | c.3009G>C (p.Lys1003Asn) c.175G>C c.1878G>C (p.Lys626Asn) c.162G>C (p.Lys54Asn) n.3865G>C | |
2 | g.29226980C>T | CA425435962 | ALK | c.3009G>A (p.Lys1003=) c.175G>A c.1878G>A (p.Lys626=) c.162G>A (p.Lys54=) n.3865G>A | |
2 | g.29226981T>A | CA346467651 | ALK | c.3008A>T (p.Lys1003Met) c.174A>T c.1877A>T (p.Lys626Met) c.161A>T (p.Lys54Met) n.3864A>T | ClinVar dbSNP gnomAD v4 |
2 | g.29226981T>C | CA346467652 | ALK | c.3008A>G (p.Lys1003Arg) c.174A>G c.1877A>G (p.Lys626Arg) c.161A>G (p.Lys54Arg) n.3864A>G | ClinVar dbSNP gnomAD v4 |
2 | g.29226981T>G | CA346467653 | ALK | c.3008A>C (p.Lys1003Thr) c.174A>C c.1877A>C (p.Lys626Thr) c.161A>C (p.Lys54Thr) n.3864A>C | |
2 | g.29226981T= | CA1241092858 | ALK | c.3008A= (p.Lys1003=) c.174A= c.1877A= (p.Lys626=) c.161A= (p.Lys54=) n.3864A= | |
2 | g.29226981_29226982dup | CA767493682 | ALK | c.3007_3008dup (p.Val1004ArgfsTer?) c.173_174dup c.1876_1877dup (p.Val627ArgfsTer?) c.160_161dup (p.Val55ArgfsTer?) n.3863_3864dup | dbSNP gnomAD v3 gnomAD v4 |
2 | g.29226982T>A | CA346467654 | ALK | c.3007A>T (p.Lys1003Ter) c.173A>T c.1876A>T (p.Lys626Ter) c.160A>T (p.Lys54Ter) n.3863A>T | dbSNP |
2 | g.29226982T>C | CA1594113 | ALK | c.3007A>G (p.Lys1003Glu) c.173A>G c.1876A>G (p.Lys626Glu) c.160A>G (p.Lys54Glu) n.3863A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29226982T>G | CA346467655 | ALK | c.3007A>C (p.Lys1003Gln) c.173A>C c.1876A>C (p.Lys626Gln) c.160A>C (p.Lys54Gln) n.3863A>C | ClinVar |
2 | g.29226982T= | CA1241092859 | ALK | c.3007A= (p.Lys1003=) c.173A= c.1876A= (p.Lys626=) c.160A= (p.Lys54=) n.3863A= | |
2 | g.29226983G>A | CA425435966 | ALK | c.3006C>T (p.His1002=) c.172C>T c.1875C>T (p.His625=) c.159C>T (p.His53=) n.3862C>T | gnomAD v4 |
2 | g.29226983G>C | CA346467656 | ALK | c.3006C>G (p.His1002Gln) c.172C>G c.1875C>G (p.His625Gln) c.159C>G (p.His53Gln) n.3862C>G | dbSNP |
2 | g.29226983G= | CA1241092860 | ALK | c.3006C= (p.His1002=) c.172C= c.1875C= (p.His625=) c.159C= (p.His53=) n.3862C= | |
2 | g.29226983G>T | CA346467657 | ALK | c.3006C>A (p.His1002Gln) c.172C>A c.1875C>A (p.His625Gln) c.159C>A (p.His53Gln) n.3862C>A | dbSNP gnomAD v2 gnomAD v4 |
2 | g.29226984T>A | CA346467658 | ALK | c.3005A>T (p.His1002Leu) c.171A>T c.1874A>T (p.His625Leu) c.158A>T (p.His53Leu) n.3861A>T | dbSNP |
2 | g.29226984T>C | CA346467659 | ALK | c.3005A>G (p.His1002Arg) c.171A>G c.1874A>G (p.His625Arg) c.158A>G (p.His53Arg) n.3861A>G | |
2 | g.29226984T>G | CA1594114 | ALK | c.3005A>C (p.His1002Pro) c.171A>C c.1874A>C (p.His625Pro) c.158A>C (p.His53Pro) n.3861A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29226984T= | CA1241092861 | ALK | c.3005A= (p.His1002=) c.171A= c.1874A= (p.His625=) c.158A= (p.His53=) n.3861A= | |
2 | g.29226985G>A | CA1594115 | ALK | c.3004C>T (p.His1002Tyr) c.170C>T c.1873C>T (p.His625Tyr) c.157C>T (p.His53Tyr) n.3860C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29226985G>C | CA346467660 | ALK | c.3004C>G (p.His1002Asp) c.170C>G c.1873C>G (p.His625Asp) c.157C>G (p.His53Asp) n.3860C>G | dbSNP |
2 | g.29226985G= | CA1241092862 | ALK | c.3004C= (p.His1002=) c.170C= c.1873C= (p.His625=) c.157C= (p.His53=) n.3860C= | |
2 | g.29226985G>T | CA346467661 | ALK | c.3004C>A (p.His1002Asn) c.170C>A c.1873C>A (p.His625Asn) c.157C>A (p.His53Asn) n.3860C>A | |
2 | g.29226986G>A | CA425435968 | ALK | c.3003C>T (p.Ser1001=) c.169C>T c.1872C>T (p.Ser624=) c.156C>T (p.Ser52=) n.3859C>T | dbSNP |
2 | g.29226986G>C | CA346467662 | ALK | c.3003C>G (p.Ser1001Arg) c.169C>G c.1872C>G (p.Ser624Arg) c.156C>G (p.Ser52Arg) n.3859C>G | dbSNP |
2 | g.29226986G>T | CA346467663 | ALK | c.3003C>A (p.Ser1001Arg) c.169C>A c.1872C>A (p.Ser624Arg) c.156C>A (p.Ser52Arg) n.3859C>A | dbSNP |
2 | g.29226987C>A | CA346467664 | ALK | c.3002G>T (p.Ser1001Ile) c.168G>T c.1871G>T (p.Ser624Ile) c.155G>T (p.Ser52Ile) n.3858G>T | dbSNP gnomAD v4 |
2 | g.29226987C= | CA1241092863 | ALK | c.3002G= (p.Ser1001=) c.168G= c.1871G= (p.Ser624=) c.155G= (p.Ser52=) n.3858G= | |
2 | g.29226987C>G | CA346467665 | ALK | c.3002G>C (p.Ser1001Thr) c.168G>C c.1871G>C (p.Ser624Thr) c.155G>C (p.Ser52Thr) n.3858G>C | dbSNP |
2 | g.29226987C>T | CA44634354 | ALK | c.3002G>A (p.Ser1001Asn) c.168G>A c.1871G>A (p.Ser624Asn) c.155G>A (p.Ser52Asn) n.3858G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29226988T>A | CA346467666 | ALK | c.3001A>T (p.Ser1001Cys) c.167A>T c.1870A>T (p.Ser624Cys) c.154A>T (p.Ser52Cys) n.3857A>T | dbSNP |
2 | g.29226988T>C | CA346467667 | ALK | c.3001A>G (p.Ser1001Gly) c.167A>G c.1870A>G (p.Ser624Gly) c.154A>G (p.Ser52Gly) n.3857A>G | ClinVar gnomAD v4 |
2 | g.29226988T>G | CA346467668 | ALK | c.3001A>C (p.Ser1001Arg) c.167A>C c.1870A>C (p.Ser624Arg) c.154A>C (p.Ser52Arg) n.3857A>C | |
2 | g.29226989T>A | CA346467669 | ALK | c.3000A>T (p.Glu1000Asp) c.166A>T c.1869A>T (p.Glu623Asp) c.153A>T (p.Glu51Asp) n.3856A>T | dbSNP |
2 | g.29226989T>C | CA425435971 | ALK | c.3000A>G (p.Glu1000=) c.166A>G c.1869A>G (p.Glu623=) c.153A>G (p.Glu51=) n.3856A>G | ClinVar gnomAD v4 |
2 | g.29226989T>G | CA346467670 | ALK | c.3000A>C (p.Glu1000Asp) c.166A>C c.1869A>C (p.Glu623Asp) c.153A>C (p.Glu51Asp) n.3856A>C | gnomAD v4 |
2 | g.29226990T>A | CA346467672 | ALK | c.2999A>T (p.Glu1000Val) c.165A>T c.1868A>T (p.Glu623Val) c.152A>T (p.Glu51Val) n.3855A>T | dbSNP |
2 | g.29226990T>C | CA1594116 | ALK | c.2999A>G (p.Glu1000Gly) c.165A>G c.1868A>G (p.Glu623Gly) c.152A>G (p.Glu51Gly) n.3855A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29226990T>G | CA346467674 | ALK | c.2999A>C (p.Glu1000Ala) c.165A>C c.1868A>C (p.Glu623Ala) c.152A>C (p.Glu51Ala) n.3855A>C | |
2 | g.29226990T= | CA1241092864 | ALK | c.2999A= (p.Glu1000=) c.165A= c.1868A= (p.Glu623=) c.152A= (p.Glu51=) n.3855A= | |
2 | g.29226991C>A | CA346467675 | ALK | c.2998G>T (p.Glu1000Ter) c.164G>T c.1867G>T (p.Glu623Ter) c.151G>T (p.Glu51Ter) n.3854G>T | |
2 | g.29226991C= | CA1241092865 | ALK | c.2998G= (p.Glu1000=) c.164G= c.1867G= (p.Glu623=) c.151G= (p.Glu51=) n.3854G= | |
2 | g.29226991C>G | CA346467677 | ALK | c.2998G>C (p.Glu1000Gln) c.164G>C c.1867G>C (p.Glu623Gln) c.151G>C (p.Glu51Gln) n.3854G>C | ClinVar dbSNP |
2 | g.29226991C>T | CA346467679 | ALK | c.2998G>A (p.Glu1000Lys) c.164G>A c.1867G>A (p.Glu623Lys) c.151G>A (p.Glu51Lys) n.3854G>A | dbSNP |
2 | g.29226992A>C | CA425435973 | ALK | c.2997T>G (p.Pro999=) c.163T>G c.1866T>G (p.Pro622=) c.150T>G (p.Pro50=) n.3853T>G | ClinVar dbSNP gnomAD v4 |
2 | g.29226992A>G | CA425435974 | ALK | c.2997T>C (p.Pro999=) c.163T>C c.1866T>C (p.Pro622=) c.150T>C (p.Pro50=) n.3853T>C | dbSNP |
2 | g.29226992A>T | CA425435975 | ALK | c.2997T>A (p.Pro999=) c.163T>A c.1866T>A (p.Pro622=) c.150T>A (p.Pro50=) n.3853T>A | dbSNP gnomAD v4 |
2 | g.29226993G>A | CA346467681 | ALK | c.2996C>T (p.Pro999Leu) c.162C>T c.1865C>T (p.Pro622Leu) c.149C>T (p.Pro50Leu) n.3852C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29226993G>C | CA346467682 | ALK | c.2996C>G (p.Pro999Arg) c.162C>G c.1865C>G (p.Pro622Arg) c.149C>G (p.Pro50Arg) n.3852C>G | dbSNP |
2 | g.29226993G= | CA1241092866 | ALK | c.2996C= (p.Pro999=) c.162C= c.1865C= (p.Pro622=) c.149C= (p.Pro50=) n.3852C= | |
2 | g.29226993G>T | CA346467684 | ALK | c.2996C>A (p.Pro999His) c.162C>A c.1865C>A (p.Pro622His) c.149C>A (p.Pro50His) n.3852C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29226994G>A | CA346467685 | ALK | c.2995C>T (p.Pro999Ser) c.161C>T c.1864C>T (p.Pro622Ser) c.148C>T (p.Pro50Ser) n.3851C>T | |
2 | g.29226994G>C | CA346467686 | ALK | c.2995C>G (p.Pro999Ala) c.161C>G c.1864C>G (p.Pro622Ala) c.148C>G (p.Pro50Ala) n.3851C>G | dbSNP |
2 | g.29226994G>T | CA346467687 | ALK | c.2995C>A (p.Pro999Thr) c.161C>A c.1864C>A (p.Pro622Thr) c.148C>A (p.Pro50Thr) n.3851C>A | |
2 | g.29226995G>A | CA425435978 | ALK | c.2994C>T (p.Asp998=) c.160C>T c.1863C>T (p.Asp621=) c.147C>T (p.Asp49=) n.3850C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29226995G>C | CA346467688 | ALK | c.2994C>G (p.Asp998Glu) c.160C>G c.1863C>G (p.Asp621Glu) c.147C>G (p.Asp49Glu) n.3850C>G | dbSNP |
2 | g.29226995G= | CA1241092867 | ALK | c.2994C= (p.Asp998=) c.160C= c.1863C= (p.Asp621=) c.147C= (p.Asp49=) n.3850C= | |
2 | g.29226995G>T | CA346467689 | ALK | c.2994C>A (p.Asp998Glu) c.160C>A c.1863C>A (p.Asp621Glu) c.147C>A (p.Asp49Glu) n.3850C>A | |
2 | g.29226996T>A | CA346467691 | ALK | c.2993A>T (p.Asp998Val) c.159A>T c.1862A>T (p.Asp621Val) c.146A>T (p.Asp49Val) n.3849A>T | ClinVar |
2 | g.29226996T>C | CA346467694 | ALK | c.2993A>G (p.Asp998Gly) c.159A>G c.1862A>G (p.Asp621Gly) c.146A>G (p.Asp49Gly) n.3849A>G | |
2 | g.29226996T>G | CA346467693 | ALK | c.2993A>C (p.Asp998Ala) c.159A>C c.1862A>C (p.Asp621Ala) c.146A>C (p.Asp49Ala) n.3849A>C | ClinVar dbSNP |
2 | g.29226996T= | CA1241092868 | ALK | c.2993A= (p.Asp998=) c.159A= c.1862A= (p.Asp621=) c.146A= (p.Asp49=) n.3849A= | |
2 | g.29226997C>A | CA346467696 | ALK | c.2992G>T (p.Asp998Tyr) c.158G>T c.1861G>T (p.Asp621Tyr) c.145G>T (p.Asp49Tyr) n.3848G>T | |
2 | g.29226997C= | CA1241092869 | ALK | c.2992G= (p.Asp998=) c.158G= c.1861G= (p.Asp621=) c.145G= (p.Asp49=) n.3848G= | |
2 | g.29226997C>G | CA346467698 | ALK | c.2992G>C (p.Asp998His) c.158G>C c.1861G>C (p.Asp621His) c.145G>C (p.Asp49His) n.3848G>C | |
2 | g.29226997C>T | CA346467697 | ALK | c.2992G>A (p.Asp998Asn) c.158G>A c.1861G>A (p.Asp621Asn) c.145G>A (p.Asp49Asn) n.3848G>A | ClinVar dbSNP |
2 | g.29226998C>A | CA346467700 | ALK | c.2991G>T (p.Met997Ile) c.157G>T c.1860G>T (p.Met620Ile) c.144G>T (p.Met48Ile) n.3847G>T | dbSNP gnomAD v4 |
2 | g.29226998C= | CA1241092870 | ALK | c.2991G= (p.Met997=) c.157G= c.1860G= (p.Met620=) c.144G= (p.Met48=) n.3847G= | |
2 | g.29226998C>G | CA346467701 | ALK | c.2991G>C (p.Met997Ile) c.157G>C c.1860G>C (p.Met620Ile) c.144G>C (p.Met48Ile) n.3847G>C | dbSNP |
2 | g.29226998C>T | CA346467703 | ALK | c.2991G>A (p.Met997Ile) c.157G>A c.1860G>A (p.Met620Ile) c.144G>A (p.Met48Ile) n.3847G>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.29226999A>C | CA346467704 | ALK | c.2990T>G (p.Met997Arg) c.156T>G c.1859T>G (p.Met620Arg) c.143T>G (p.Met48Arg) n.3846T>G | dbSNP |
2 | g.29226999A>G | CA346467706 | ALK | c.2990T>C (p.Met997Thr) c.156T>C c.1859T>C (p.Met620Thr) c.143T>C (p.Met48Thr) n.3846T>C | ClinVar gnomAD v4 |
2 | g.29226999A>T | CA346467707 | ALK | c.2990T>A (p.Met997Lys) c.156T>A c.1859T>A (p.Met620Lys) c.143T>A (p.Met48Lys) n.3846T>A | ClinVar dbSNP gnomAD v4 |
2 | g.29227000T>A | CA346467708 | ALK | c.2989A>T (p.Met997Leu) c.155A>T c.1858A>T (p.Met620Leu) c.142A>T (p.Met48Leu) n.3845A>T | |
2 | g.29227000T>C | CA346467710 | ALK | c.2989A>G (p.Met997Val) c.155A>G c.1858A>G (p.Met620Val) c.142A>G (p.Met48Val) n.3845A>G | ClinVar |
2 | g.29227000T>G | CA346467713 | ALK | c.2989A>C (p.Met997Leu) c.155A>C c.1858A>C (p.Met620Leu) c.142A>C (p.Met48Leu) n.3845A>C | |
2 | g.29227000T= | CA1241092871 | ALK | c.2989A= (p.Met997=) c.155A= c.1858A= (p.Met620=) c.142A= (p.Met48=) n.3845A= | |
2 | g.29227001G>A | CA425435983 | ALK | c.2988C>T (p.His996=) c.154C>T c.1857C>T (p.His619=) c.141C>T (p.His47=) n.3844C>T | ClinVar dbSNP gnomAD v4 |
2 | g.29227001G>C | CA346467715 | ALK | c.2988C>G (p.His996Gln) c.154C>G c.1857C>G (p.His619Gln) c.141C>G (p.His47Gln) n.3844C>G | dbSNP |
2 | g.29227001G>T | CA346467716 | ALK | c.2988C>A (p.His996Gln) c.154C>A c.1857C>A (p.His619Gln) c.141C>A (p.His47Gln) n.3844C>A | |
2 | g.29227001dup | CA915943770 | ALK | c.2988dup (p.Met997HisfsTer4) c.154dup c.1857dup (p.Met620HisfsTer4) c.141dup (p.Met48HisfsTer4) n.3844dup | ClinVar dbSNP |
2 | g.29227002T>A | CA346467720 | ALK | c.2987A>T (p.His996Leu) c.153A>T c.1856A>T (p.His619Leu) c.140A>T (p.His47Leu) n.3843A>T | dbSNP |
2 | g.29227002T>C | CA1594117 | ALK | c.2987A>G (p.His996Arg) c.153A>G c.1856A>G (p.His619Arg) c.140A>G (p.His47Arg) n.3843A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29227002T>G | CA346467719 | ALK | c.2987A>C (p.His996Pro) c.153A>C c.1856A>C (p.His619Pro) c.140A>C (p.His47Pro) n.3843A>C | dbSNP gnomAD v4 |
2 | g.29227002T= | CA1241092872 | ALK | c.2987A= (p.His996=) c.153A= c.1856A= (p.His619=) c.140A= (p.His47=) n.3843A= | |
2 | g.29227003G>A | CA346467723 | ALK | c.2986C>T (p.His996Tyr) c.152C>T c.1855C>T (p.His619Tyr) c.139C>T (p.His47Tyr) n.3842C>T | dbSNP |
2 | g.29227003G>C | CA346467724 | ALK | c.2986C>G (p.His996Asp) c.152C>G c.1855C>G (p.His619Asp) c.139C>G (p.His47Asp) n.3842C>G | dbSNP |
2 | g.29227003G>T | CA346467726 | ALK | c.2986C>A (p.His996Asn) c.152C>A c.1855C>A (p.His619Asn) c.139C>A (p.His47Asn) n.3842C>A | dbSNP |
2 | g.29227004A>C | CA346467729 | ALK | c.2985T>G (p.Cys995Trp) c.151T>G c.1854T>G (p.Cys618Trp) c.138T>G (p.Cys46Trp) n.3841T>G | |
2 | g.29227004A>G | CA425435988 | ALK | c.2985T>C (p.Cys995=) c.151T>C c.1854T>C (p.Cys618=) c.138T>C (p.Cys46=) n.3841T>C | ClinVar |
2 | g.29227004A>T | CA346467730 | ALK | c.2985T>A (p.Cys995Ter) c.151T>A c.1854T>A (p.Cys618Ter) c.138T>A (p.Cys46Ter) n.3841T>A | dbSNP |
2 | g.29227005C>A | CA346467732 | ALK | c.2984G>T (p.Cys995Phe) c.150G>T c.1853G>T (p.Cys618Phe) c.137G>T (p.Cys46Phe) n.3840G>T | dbSNP |
2 | g.29227005C>G | CA346467734 | ALK | c.2984G>C (p.Cys995Ser) c.150G>C c.1853G>C (p.Cys618Ser) c.137G>C (p.Cys46Ser) n.3840G>C | dbSNP |
2 | g.29227005C>T | CA346467735 | ALK | c.2984G>A (p.Cys995Tyr) c.150G>A c.1853G>A (p.Cys618Tyr) c.137G>A (p.Cys46Tyr) n.3840G>A | dbSNP |
2 | g.29227006A= | CA1241092873 | ALK | c.2983T= (p.Cys995=) c.149T= c.1852T= (p.Cys618=) c.136T= (p.Cys46=) n.3839T= | |
2 | g.29227006A>C | CA346467737 | ALK | c.2983T>G (p.Cys995Gly) c.149T>G c.1852T>G (p.Cys618Gly) c.136T>G (p.Cys46Gly) n.3839T>G | dbSNP |
2 | g.29227006A>G | CA346467739 | ALK | c.2983T>C (p.Cys995Arg) c.149T>C c.1852T>C (p.Cys618Arg) c.136T>C (p.Cys46Arg) n.3839T>C | dbSNP |
2 | g.29227006A>T | CA346467741 | ALK | c.2983T>A (p.Cys995Ser) c.149T>A c.1852T>A (p.Cys618Ser) c.136T>A (p.Cys46Ser) n.3839T>A | dbSNP |
2 | g.29227007T>A | CA346467745 | ALK | c.2982A>T (p.Glu994Asp) c.148A>T c.1851A>T (p.Glu617Asp) c.135A>T (p.Glu45Asp) n.3838A>T | ClinVar dbSNP |
2 | g.29227007T>C | CA425435990 | ALK | c.2982A>G (p.Glu994=) c.148A>G c.1851A>G (p.Glu617=) c.135A>G (p.Glu45=) n.3838A>G | dbSNP |
2 | g.29227007T>G | CA346467743 | ALK | c.2982A>C (p.Glu994Asp) c.148A>C c.1851A>C (p.Glu617Asp) c.135A>C (p.Glu45Asp) n.3838A>C | dbSNP |
2 | g.29227008dup | CA767493735 | ALK | c.2982dup (p.Cys995MetfsTer6) c.148dup c.1851dup (p.Cys618MetfsTer6) c.135dup (p.Cys46MetfsTer6) n.3838dup | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29227008T>A | CA346467747 | ALK | c.2981A>T (p.Glu994Val) c.147A>T c.1850A>T (p.Glu617Val) c.134A>T (p.Glu45Val) n.3837A>T | dbSNP |
2 | g.29227008T>C | CA346467750 | ALK | c.2981A>G (p.Glu994Gly) c.147A>G c.1850A>G (p.Glu617Gly) c.134A>G (p.Glu45Gly) n.3837A>G | dbSNP |
2 | g.29227008T>G | CA346467752 | ALK | c.2981A>C (p.Glu994Ala) c.147A>C c.1850A>C (p.Glu617Ala) c.134A>C (p.Glu45Ala) n.3837A>C | |
2 | g.29227009C>A | CA346467755 | ALK | c.2980G>T (p.Glu994Ter) c.146G>T c.1849G>T (p.Glu617Ter) c.133G>T (p.Glu45Ter) n.3836G>T | dbSNP |
2 | g.29227009C= | CA1241092874 | ALK | c.2980G= (p.Glu994=) c.146G= c.1849G= (p.Glu617=) c.133G= (p.Glu45=) n.3836G= | |
2 | g.29227009C>G | CA346467756 | ALK | c.2980G>C (p.Glu994Gln) c.146G>C c.1849G>C (p.Glu617Gln) c.133G>C (p.Glu45Gln) n.3836G>C | dbSNP |
2 | g.29227009C>T | CA1594118 | ALK | c.2980G>A (p.Glu994Lys) c.146G>A c.1849G>A (p.Glu617Lys) c.133G>A (p.Glu45Lys) n.3836G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29227010G>A | CA1594119 | ALK | c.2979C>T (p.Asp993=) c.145C>T c.1848C>T (p.Asp616=) c.132C>T (p.Asp44=) n.3835C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29227010G>C | CA346467763 | ALK | c.2979C>G (p.Asp993Glu) c.145C>G c.1848C>G (p.Asp616Glu) c.132C>G (p.Asp44Glu) n.3835C>G | dbSNP |
2 | g.29227010G= | CA1241092875 | ALK | c.2979C= (p.Asp993=) c.145C= c.1848C= (p.Asp616=) c.132C= (p.Asp44=) n.3835C= | |
2 | g.29227010G>T | CA346467765 | ALK | c.2979C>A (p.Asp993Glu) c.145C>A c.1848C>A (p.Asp616Glu) c.132C>A (p.Asp44Glu) n.3835C>A | ClinVar dbSNP gnomAD v4 |
2 | g.29227011T>A | CA346467766 | ALK | c.2978A>T (p.Asp993Val) c.144A>T c.1847A>T (p.Asp616Val) c.131A>T (p.Asp44Val) n.3834A>T | ClinVar dbSNP gnomAD v4 |
2 | g.29227011T>C | CA346467767 | ALK | c.2978A>G (p.Asp993Gly) c.144A>G c.1847A>G (p.Asp616Gly) c.131A>G (p.Asp44Gly) n.3834A>G | ClinVar dbSNP gnomAD v4 |
2 | g.29227011T>G | CA346467768 | ALK | c.2978A>C (p.Asp993Ala) c.144A>C c.1847A>C (p.Asp616Ala) c.131A>C (p.Asp44Ala) n.3834A>C | |
2 | g.29227011T= | CA1241092876 | ALK | c.2978A= (p.Asp993=) c.144A= c.1847A= (p.Asp616=) c.131A= (p.Asp44=) n.3834A= | |
2 | g.29227012C>A | CA346467771 | ALK | c.2977G>T (p.Asp993Tyr) c.143G>T c.1846G>T (p.Asp616Tyr) c.130G>T (p.Asp44Tyr) n.3833G>T | dbSNP |
2 | g.29227012C>G | CA346467774 | ALK | c.2977G>C (p.Asp993His) c.143G>C c.1846G>C (p.Asp616His) c.130G>C (p.Asp44His) n.3833G>C | ClinVar dbSNP |
2 | g.29227012C>T | CA346467770 | ALK | c.2977G>A (p.Asp993Asn) c.143G>A c.1846G>A (p.Asp616Asn) c.130G>A (p.Asp44Asn) n.3833G>A | ClinVar dbSNP gnomAD v4 |
2 | g.29227013T>A | CA425435991 | ALK | c.2976A>T (p.Val992=) c.142A>T c.1845A>T (p.Val615=) c.129A>T (p.Val43=) n.3832A>T | dbSNP |
2 | g.29227013T>C | CA425435992 | ALK | c.2976A>G (p.Val992=) c.142A>G c.1845A>G (p.Val615=) c.129A>G (p.Val43=) n.3832A>G | ClinVar dbSNP |
2 | g.29227013T>G | CA425435993 | ALK | c.2976A>C (p.Val992=) c.142A>C c.1845A>C (p.Val615=) c.129A>C (p.Val43=) n.3832A>C | |
2 | g.29227014A>C | CA346467776 | ALK | c.2975T>G (p.Val992Gly) c.141T>G c.1844T>G (p.Val615Gly) c.128T>G (p.Val43Gly) n.3831T>G | dbSNP |
2 | g.29227014A>G | CA346467777 | ALK | c.2975T>C (p.Val992Ala) c.141T>C c.1844T>C (p.Val615Ala) c.128T>C (p.Val43Ala) n.3831T>C | |
2 | g.29227014A>T | CA346467780 | ALK | c.2975T>A (p.Val992Glu) c.141T>A c.1844T>A (p.Val615Glu) c.128T>A (p.Val43Glu) n.3831T>A | dbSNP |
2 | g.29227015C>A | CA346467784 | ALK | c.2974G>T (p.Val992Leu) c.140G>T c.1843G>T (p.Val615Leu) c.127G>T (p.Val43Leu) n.3830G>T | dbSNP |
2 | g.29227015C>G | CA346467786 | ALK | c.2974G>C (p.Val992Leu) c.140G>C c.1843G>C (p.Val615Leu) c.127G>C (p.Val43Leu) n.3830G>C | dbSNP gnomAD v4 |
2 | g.29227015C>T | CA346467787 | ALK | c.2974G>A (p.Val992Ile) c.140G>A c.1843G>A (p.Val615Ile) c.127G>A (p.Val43Ile) n.3830G>A | dbSNP gnomAD v4 |
2 | g.29227016C>A | CA346467789 | ALK | c.2973G>T (p.Glu991Asp) c.139G>T c.1842G>T (p.Glu614Asp) c.126G>T (p.Glu42Asp) n.3829G>T | |
2 | g.29227016C= | CA1241092877 | ALK | c.2973G= (p.Glu991=) c.139G= c.1842G= (p.Glu614=) c.126G= (p.Glu42=) n.3829G= | |
2 | g.29227016C>G | CA346467794 | ALK | c.2973G>C (p.Glu991Asp) c.139G>C c.1842G>C (p.Glu614Asp) c.126G>C (p.Glu42Asp) n.3829G>C | gnomAD v4 |
2 | g.29227016C>T | CA425435994 | ALK | c.2973G>A (p.Glu991=) c.139G>A c.1842G>A (p.Glu614=) c.126G>A (p.Glu42=) n.3829G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29227017T>A | CA346467796 | ALK | c.2972A>T (p.Glu991Val) c.138A>T c.1841A>T (p.Glu614Val) c.125A>T (p.Glu42Val) n.3828A>T | dbSNP |
2 | g.29227017T>C | CA346467798 | ALK | c.2972A>G (p.Glu991Gly) c.138A>G c.1841A>G (p.Glu614Gly) c.125A>G (p.Glu42Gly) n.3828A>G | dbSNP |
2 | g.29227017T>G | CA346467804 | ALK | c.2972A>C (p.Glu991Ala) c.138A>C c.1841A>C (p.Glu614Ala) c.125A>C (p.Glu42Ala) n.3828A>C | |
2 | g.29227018C>A | CA346467812 | ALK | c.2971G>T (p.Glu991Ter) c.137G>T c.1840G>T (p.Glu614Ter) c.124G>T (p.Glu42Ter) n.3827G>T | dbSNP |
2 | g.29227018C>G | CA346467813 | ALK | c.2971G>C (p.Glu991Gln) c.137G>C c.1840G>C (p.Glu614Gln) c.124G>C (p.Glu42Gln) n.3827G>C | dbSNP |
2 | g.29227018C>T | CA346467820 | ALK | c.2971G>A (p.Glu991Lys) c.137G>A c.1840G>A (p.Glu614Lys) c.124G>A (p.Glu42Lys) n.3827G>A | dbSNP |
2 | g.29227020_29227021del | CA2697547961 | ALK | c.2970_2971del (p.Cys990Ter) c.136_137del c.1839_1840del (p.Cys613Ter) c.123_124del (p.Cys41Ter) n.3826_3827del | ClinVar |
2 | g.29227019A>C | CA346467824 | ALK | c.2970T>G (p.Cys990Trp) c.136T>G c.1839T>G (p.Cys613Trp) c.123T>G (p.Cys41Trp) n.3826T>G | gnomAD v4 |
2 | g.29227019A>G | CA425435995 | ALK | c.2970T>C (p.Cys990=) c.136T>C c.1839T>C (p.Cys613=) c.123T>C (p.Cys41=) n.3826T>C | dbSNP |
2 | g.29227019A>T | CA346467826 | ALK | c.2970T>A (p.Cys990Ter) c.136T>A c.1839T>A (p.Cys613Ter) c.123T>A (p.Cys41Ter) n.3826T>A | dbSNP |
2 | g.29227020C>A | CA346467835 | ALK | c.2969G>T (p.Cys990Phe) c.135G>T c.1838G>T (p.Cys613Phe) c.122G>T (p.Cys41Phe) n.3825G>T | dbSNP |
2 | g.29227020C>G | CA346467845 | ALK | c.2969G>C (p.Cys990Ser) c.135G>C c.1838G>C (p.Cys613Ser) c.122G>C (p.Cys41Ser) n.3825G>C | dbSNP |
2 | g.29227020C>T | CA346467836 | ALK | c.2969G>A (p.Cys990Tyr) c.135G>A c.1838G>A (p.Cys613Tyr) c.122G>A (p.Cys41Tyr) n.3825G>A | dbSNP |
2 | g.29227021A>C | CA346467851 | ALK | c.2968T>G (p.Cys990Gly) c.134T>G c.1837T>G (p.Cys613Gly) c.121T>G (p.Cys41Gly) n.3824T>G | |
2 | g.29227021A>G | CA346467853 | ALK | c.2968T>C (p.Cys990Arg) c.134T>C c.1837T>C (p.Cys613Arg) c.121T>C (p.Cys41Arg) n.3824T>C | dbSNP |
2 | g.29227021A>T | CA346467854 | ALK | c.2968T>A (p.Cys990Ser) c.134T>A c.1837T>A (p.Cys613Ser) c.121T>A (p.Cys41Ser) n.3824T>A | |
2 | g.29227022G>A | CA425435996 | ALK | c.2967C>T (p.His989=) c.133C>T c.1836C>T (p.His612=) c.120C>T (p.His40=) n.3823C>T | ClinVar dbSNP |
2 | g.29227022G>C | CA346467857 | ALK | c.2967C>G (p.His989Gln) c.133C>G c.1836C>G (p.His612Gln) c.120C>G (p.His40Gln) n.3823C>G | dbSNP |
2 | g.29227022G>T | CA346467858 | ALK | c.2967C>A (p.His989Gln) c.133C>A c.1836C>A (p.His612Gln) c.120C>A (p.His40Gln) n.3823C>A | |
2 | g.29227023T>A | CA346467860 | ALK | c.2966A>T (p.His989Leu) c.132A>T c.1835A>T (p.His612Leu) c.119A>T (p.His40Leu) n.3822A>T | dbSNP |
2 | g.29227023T>C | CA346467868 | ALK | c.2966A>G (p.His989Arg) c.132A>G c.1835A>G (p.His612Arg) c.119A>G (p.His40Arg) n.3822A>G | |
2 | g.29227023T>G | CA346467871 | ALK | c.2966A>C (p.His989Pro) c.132A>C c.1835A>C (p.His612Pro) c.119A>C (p.His40Pro) n.3822A>C | gnomAD v4 |
2 | g.29227024G>A | CA346467873 | ALK | c.2965C>T (p.His989Tyr) c.131C>T c.1834C>T (p.His612Tyr) c.118C>T (p.His40Tyr) n.3821C>T | ClinVar dbSNP gnomAD v4 |
2 | g.29227024G>C | CA346467875 | ALK | c.2965C>G (p.His989Asp) c.131C>G c.1834C>G (p.His612Asp) c.118C>G (p.His40Asp) n.3821C>G | dbSNP |
2 | g.29227024G= | CA1241092878 | ALK | c.2965C= (p.His989=) c.131C= c.1834C= (p.His612=) c.118C= (p.His40=) n.3821C= | |
2 | g.29227024G>T | CA346467879 | ALK | c.2965C>A (p.His989Asn) c.131C>A c.1834C>A (p.His612Asn) c.118C>A (p.His40Asn) n.3821C>A | ClinVar gnomAD v4 |
2 | g.29227025A>C | CA346467880 | ALK | c.2964T>G (p.Ser988Arg) c.130T>G c.1833T>G (p.Ser611Arg) c.117T>G (p.Ser39Arg) n.3820T>G | |
2 | g.29227025A>G | CA425435997 | ALK | c.2964T>C (p.Ser988=) c.130T>C c.1833T>C (p.Ser611=) c.117T>C (p.Ser39=) n.3820T>C | dbSNP gnomAD v4 |
2 | g.29227025A>T | CA346467882 | ALK | c.2964T>A (p.Ser988Arg) c.130T>A c.1833T>A (p.Ser611Arg) c.117T>A (p.Ser39Arg) n.3820T>A | dbSNP gnomAD v4 |
2 | g.29227026C>A | CA346467887 | ALK | c.2963G>T (p.Ser988Ile) c.129G>T c.1832G>T (p.Ser611Ile) c.116G>T (p.Ser39Ile) n.3819G>T | dbSNP |
2 | g.29227026C>G | CA346467891 | ALK | c.2963G>C (p.Ser988Thr) c.129G>C c.1832G>C (p.Ser611Thr) c.116G>C (p.Ser39Thr) n.3819G>C | dbSNP |
2 | g.29227026C>T | CA346467888 | ALK | c.2963G>A (p.Ser988Asn) c.129G>A c.1832G>A (p.Ser611Asn) c.116G>A (p.Ser39Asn) n.3819G>A | dbSNP |
2 | g.29227027T>A | CA346467894 | ALK | c.2962A>T (p.Ser988Cys) c.128A>T c.1831A>T (p.Ser611Cys) c.115A>T (p.Ser39Cys) n.3818A>T | dbSNP |
2 | g.29227027T>C | CA346467896 | ALK | c.2962A>G (p.Ser988Gly) c.128A>G c.1831A>G (p.Ser611Gly) c.115A>G (p.Ser39Gly) n.3818A>G | dbSNP |
2 | g.29227027T>G | CA346467898 | ALK | c.2962A>C (p.Ser988Arg) c.128A>C c.1831A>C (p.Ser611Arg) c.115A>C (p.Ser39Arg) n.3818A>C | ClinVar dbSNP |
2 | g.29227028G>A | CA425435998 | ALK | c.2961C>T (p.Cys987=) c.127C>T c.1830C>T (p.Cys610=) c.114C>T (p.Cys38=) n.3817C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.29227028G>C | CA346467904 | ALK | c.2961C>G (p.Cys987Trp) c.127C>G c.1830C>G (p.Cys610Trp) c.114C>G (p.Cys38Trp) n.3817C>G | dbSNP |
2 | g.29227028G= | CA1241092879 | ALK | c.2961C= (p.Cys987=) c.127C= c.1830C= (p.Cys610=) c.114C= (p.Cys38=) n.3817C= | |
2 | g.29227028G>T | CA346467907 | ALK | c.2961C>A (p.Cys987Ter) c.127C>A c.1830C>A (p.Cys610Ter) c.114C>A (p.Cys38Ter) n.3817C>A | |
2 | g.29227029C>A | CA346467909 | ALK | c.2960G>T (p.Cys987Phe) c.126G>T c.1829G>T (p.Cys610Phe) c.113G>T (p.Cys38Phe) n.3816G>T | dbSNP |
2 | g.29227029C>G | CA346467914 | ALK | c.2960G>C (p.Cys987Ser) c.126G>C c.1829G>C (p.Cys610Ser) c.113G>C (p.Cys38Ser) n.3816G>C | ClinVar dbSNP |
2 | g.29227029C>T | CA346467915 | ALK | c.2960G>A (p.Cys987Tyr) c.126G>A c.1829G>A (p.Cys610Tyr) c.113G>A (p.Cys38Tyr) n.3816G>A | dbSNP |
2 | g.29227030A= | CA1241092880 | ALK | c.2959T= (p.Cys987=) c.125T= c.1828T= (p.Cys610=) c.112T= (p.Cys38=) n.3815T= | |
2 | g.29227030A>C | CA346467917 | ALK | c.2959T>G (p.Cys987Gly) c.125T>G c.1828T>G (p.Cys610Gly) c.112T>G (p.Cys38Gly) n.3815T>G | dbSNP |
2 | g.29227030A>G | CA346467921 | ALK | c.2959T>C (p.Cys987Arg) c.125T>C c.1828T>C (p.Cys610Arg) c.112T>C (p.Cys38Arg) n.3815T>C | dbSNP |
2 | g.29227030A>T | CA346467923 | ALK | c.2959T>A (p.Cys987Ser) c.125T>A c.1828T>A (p.Cys610Ser) c.112T>A (p.Cys38Ser) n.3815T>A | dbSNP |
2 | g.29227031G>A | CA425435999 | ALK | c.2958C>T (p.Asn986=) c.124C>T c.1827C>T (p.Asn609=) c.111C>T (p.Asn37=) n.3814C>T | ClinVar dbSNP gnomAD v4 |
2 | g.29227031G>C | CA346467926 | ALK | c.2958C>G (p.Asn986Lys) c.124C>G c.1827C>G (p.Asn609Lys) c.111C>G (p.Asn37Lys) n.3814C>G | |
2 | g.29227031G>T | CA346467928 | ALK | c.2958C>A (p.Asn986Lys) c.124C>A c.1827C>A (p.Asn609Lys) c.111C>A (p.Asn37Lys) n.3814C>A | |
2 | g.29227032T>A | CA346467930 | ALK | c.2957A>T (p.Asn986Ile) c.123A>T c.1826A>T (p.Asn609Ile) c.110A>T (p.Asn37Ile) n.3813A>T | dbSNP |
2 | g.29227032T>C | CA346467933 | ALK | c.2957A>G (p.Asn986Ser) c.123A>G c.1826A>G (p.Asn609Ser) c.110A>G (p.Asn37Ser) n.3813A>G | dbSNP |
2 | g.29227032T>G | CA346467934 | ALK | c.2957A>C (p.Asn986Thr) c.123A>C c.1826A>C (p.Asn609Thr) c.110A>C (p.Asn37Thr) n.3813A>C | |
2 | g.29227032T= | CA1241092881 | ALK | c.2957A= (p.Asn986=) c.123A= c.1826A= (p.Asn609=) c.110A= (p.Asn37=) n.3813A= | |
2 | g.29227033T>A | CA346467935 | ALK | c.2956A>T (p.Asn986Tyr) c.122A>T c.1825A>T (p.Asn609Tyr) c.109A>T (p.Asn37Tyr) n.3812A>T | dbSNP |
2 | g.29227033T>C | CA346467937 | ALK | c.2956A>G (p.Asn986Asp) c.122A>G c.1825A>G (p.Asn609Asp) c.109A>G (p.Asn37Asp) n.3812A>G | dbSNP |
2 | g.29227033T>G | CA346467939 | ALK | c.2956A>C (p.Asn986His) c.122A>C c.1825A>C (p.Asn609His) c.109A>C (p.Asn37His) n.3812A>C | |
2 | g.29227034T>A | CA425436000 | ALK | c.2955A>T (p.Leu985=) c.121A>T c.1824A>T (p.Leu608=) c.108A>T (p.Leu36=) n.3811A>T | dbSNP |
2 | g.29227034T>C | CA425436001 | ALK | c.2955A>G (p.Leu985=) c.121A>G c.1824A>G (p.Leu608=) c.108A>G (p.Leu36=) n.3811A>G | |
2 | g.29227034T>G | CA425436002 | ALK | c.2955A>C (p.Leu985=) c.121A>C c.1824A>C (p.Leu608=) c.108A>C (p.Leu36=) n.3811A>C | |
2 | g.29227035A>C | CA346467942 | ALK | c.2954T>G (p.Leu985Arg) c.120T>G c.1823T>G (p.Leu608Arg) c.107T>G (p.Leu36Arg) n.3810T>G | |
2 | g.29227035A>G | CA346467943 | ALK | c.2954T>C (p.Leu985Pro) c.120T>C c.1823T>C (p.Leu608Pro) c.107T>C (p.Leu36Pro) n.3810T>C | dbSNP |
2 | g.29227035A>T | CA346467944 | ALK | c.2954T>A (p.Leu985Gln) c.120T>A c.1823T>A (p.Leu608Gln) c.107T>A (p.Leu36Gln) n.3810T>A | dbSNP |
2 | g.29227036G>A | CA425436003 | ALK | c.2953C>T (p.Leu985=) c.119C>T c.1822C>T (p.Leu608=) c.106C>T (p.Leu36=) n.3809C>T | ClinVar dbSNP |
2 | g.29227036G>C | CA346467946 | ALK | c.2953C>G (p.Leu985Val) c.119C>G c.1822C>G (p.Leu608Val) c.106C>G (p.Leu36Val) n.3809C>G | dbSNP |
2 | g.29227036G>T | CA346467949 | ALK | c.2953C>A (p.Leu985Ile) c.119C>A c.1822C>A (p.Leu608Ile) c.106C>A (p.Leu36Ile) n.3809C>A | |
2 | g.29227037A= | CA1241092882 | ALK | c.2952T= (p.Tyr984=) c.118T= c.1821T= (p.Tyr607=) c.105T= (p.Tyr35=) n.3808T= | |
2 | g.29227037A>C | CA346467950 | ALK | c.2952T>G (p.Tyr984Ter) c.118T>G c.1821T>G (p.Tyr607Ter) c.105T>G (p.Tyr35Ter) n.3808T>G | ClinVar dbSNP |
2 | g.29227037A>G | CA425436004 | ALK | c.2952T>C (p.Tyr984=) c.118T>C c.1821T>C (p.Tyr607=) c.105T>C (p.Tyr35=) n.3808T>C | |
2 | g.29227037A>T | CA346467951 | ALK | c.2952T>A (p.Tyr984Ter) c.118T>A c.1821T>A (p.Tyr607Ter) c.105T>A (p.Tyr35Ter) n.3808T>A | |
2 | g.29227039_29227041del | CA2658460449 | ALK | c.2950_2952del (p.Tyr984del) c.116_118del c.1819_1821del (p.Tyr607del) c.103_105del (p.Tyr35del) n.3806_3808del | gnomAD v4 |
2 | g.29227038T>A | CA346467953 | ALK | c.2951A>T (p.Tyr984Phe) c.117A>T c.1820A>T (p.Tyr607Phe) c.104A>T (p.Tyr35Phe) n.3807A>T | dbSNP |
2 | g.29227038T>C | CA346467952 | ALK | c.2951A>G (p.Tyr984Cys) c.117A>G c.1820A>G (p.Tyr607Cys) c.104A>G (p.Tyr35Cys) n.3807A>G | COSMIC |
2 | g.29227038T>G | CA1594120 | ALK | c.2951A>C (p.Tyr984Ser) c.117A>C c.1820A>C (p.Tyr607Ser) c.104A>C (p.Tyr35Ser) n.3807A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.29227038T= | CA1241092883 | ALK | c.2951A= (p.Tyr984=) c.117A= c.1820A= (p.Tyr607=) c.104A= (p.Tyr35=) n.3807A= | |
2 | g.29227039A= | CA1241092884 | ALK | c.2950T= (p.Tyr984=) c.116T= c.1819T= (p.Tyr607=) c.103T= (p.Tyr35=) n.3806T= | |
2 | g.29227039A>C | CA346467955 | ALK | c.2950T>G (p.Tyr984Asp) c.116T>G c.1819T>G (p.Tyr607Asp) c.103T>G (p.Tyr35Asp) n.3806T>G | |
2 | g.29227039A>G | CA346467962 | ALK | c.2950T>C (p.Tyr984His) c.116T>C c.1819T>C (p.Tyr607His) c.103T>C (p.Tyr35His) n.3806T>C | ClinVar dbSNP |
2 | g.29227039A>T | CA346467963 | ALK | c.2950T>A (p.Tyr984Asn) c.116T>A c.1819T>A (p.Tyr607Asn) c.103T>A (p.Tyr35Asn) n.3806T>A | dbSNP |
2 | g.29227040A= | CA1241092885 | ALK | c.2949T= (p.His983=) c.115T= c.1818T= (p.His606=) c.102T= (p.His34=) n.3805T= | |
2 | g.29227040A>C | CA346467966 | ALK | c.2949T>G (p.His983Gln) c.115T>G c.1818T>G (p.His606Gln) c.102T>G (p.His34Gln) n.3805T>G | |
2 | g.29227040A>G | CA44634365 | ALK | c.2949T>C (p.His983=) c.115T>C c.1818T>C (p.His606=) c.102T>C (p.His34=) n.3805T>C | ClinVar dbSNP gnomAD v4 |
2 | g.29227040A>T | CA346467975 | ALK | c.2949T>A (p.His983Gln) c.115T>A c.1818T>A (p.His606Gln) c.102T>A (p.His34Gln) n.3805T>A | |
2 | g.29227041T>A | CA346467978 | ALK | c.2948A>T (p.His983Leu) c.114A>T c.1817A>T (p.His606Leu) c.101A>T (p.His34Leu) n.3804A>T | dbSNP |
2 | g.29227041T>C | CA346467980 | ALK | c.2948A>G (p.His983Arg) c.114A>G c.1817A>G (p.His606Arg) c.101A>G (p.His34Arg) n.3804A>G | ClinVar |
2 | g.29227041T>G | CA346467983 | ALK | c.2948A>C (p.His983Pro) c.114A>C c.1817A>C (p.His606Pro) c.101A>C (p.His34Pro) n.3804A>C | |
2 | g.29227042G>A | CA346467986 | ALK | c.2947C>T (p.His983Tyr) c.113C>T c.1816C>T (p.His606Tyr) c.100C>T (p.His34Tyr) n.3803C>T | ClinVar dbSNP |
2 | g.29227042G>C | CA346467989 | ALK | c.2947C>G (p.His983Asp) c.113C>G c.1816C>G (p.His606Asp) c.100C>G (p.His34Asp) n.3803C>G | dbSNP |
2 | g.29227042G>T | CA346467993 | ALK | c.2947C>A (p.His983Asn) c.113C>A c.1816C>A (p.His606Asn) c.100C>A (p.His34Asn) n.3803C>A | dbSNP |
2 | g.29227043C>A | CA346467998 | ALK | c.2946G>T (p.Lys982Asn) c.112G>T c.1815G>T (p.Lys605Asn) c.99G>T (p.Lys33Asn) n.3802G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29227043C= | CA1241092886 | ALK | c.2946G= (p.Lys982=) c.112G= c.1815G= (p.Lys605=) c.99G= (p.Lys33=) n.3802G= | |
2 | g.29227043C>G | CA346467995 | ALK | c.2946G>C (p.Lys982Asn) c.112G>C c.1815G>C (p.Lys605Asn) c.99G>C (p.Lys33Asn) n.3802G>C | dbSNP |
2 | g.29227043C>T | CA425436005 | ALK | c.2946G>A (p.Lys982=) c.112G>A c.1815G>A (p.Lys605=) c.99G>A (p.Lys33=) n.3802G>A | dbSNP |
2 | g.29227044T>A | CA346468003 | ALK | c.2945A>T (p.Lys982Met) c.111A>T c.1814A>T (p.Lys605Met) c.98A>T (p.Lys33Met) n.3801A>T | dbSNP |
2 | g.29227044T>C | CA346468005 | ALK | c.2945A>G (p.Lys982Arg) c.111A>G c.1814A>G (p.Lys605Arg) c.98A>G (p.Lys33Arg) n.3801A>G | |
2 | g.29227044T>G | CA346468004 | ALK | c.2945A>C (p.Lys982Thr) c.111A>C c.1814A>C (p.Lys605Thr) c.98A>C (p.Lys33Thr) n.3801A>C | |
2 | g.29227045T>A | CA346468007 | ALK | c.2944A>T (p.Lys982Ter) c.110A>T c.1813A>T (p.Lys605Ter) c.97A>T (p.Lys33Ter) n.3800A>T | dbSNP |
2 | g.29227045T>C | CA346468011 | ALK | c.2944A>G (p.Lys982Glu) c.110A>G c.1813A>G (p.Lys605Glu) c.97A>G (p.Lys33Glu) n.3800A>G | dbSNP |
2 | g.29227045T>G | CA346468009 | ALK | c.2944A>C (p.Lys982Gln) c.110A>C c.1813A>C (p.Lys605Gln) c.97A>C (p.Lys33Gln) n.3800A>C | |
2 | g.29227046A>C | CA346468013 | ALK | c.2943T>G (p.Ile981Met) c.109T>G c.1812T>G (p.Ile604Met) c.96T>G (p.Ile32Met) n.3799T>G | |
2 | g.29227046A>G | CA425436007 | ALK | c.2943T>C (p.Ile981=) c.109T>C c.1812T>C (p.Ile604=) c.96T>C (p.Ile32=) n.3799T>C | |
2 | g.29227046A>T | CA425436008 | ALK | c.2943T>A (p.Ile981=) c.109T>A c.1812T>A (p.Ile604=) c.96T>A (p.Ile32=) n.3799T>A | dbSNP |
2 | g.29227047A>C | CA346468015 | ALK | c.2942T>G (p.Ile981Ser) c.108T>G c.1811T>G (p.Ile604Ser) c.95T>G (p.Ile32Ser) n.3798T>G | |
2 | g.29227047A>G | CA346468016 | ALK | c.2942T>C (p.Ile981Thr) c.108T>C c.1811T>C (p.Ile604Thr) c.95T>C (p.Ile32Thr) n.3798T>C | |
2 | g.29227047A>T | CA346468019 | ALK | c.2942T>A (p.Ile981Asn) c.108T>A c.1811T>A (p.Ile604Asn) c.95T>A (p.Ile32Asn) n.3798T>A | dbSNP |
2 | g.29227048T>A | CA346468022 | ALK | c.2941A>T (p.Ile981Phe) c.107A>T c.1810A>T (p.Ile604Phe) c.94A>T (p.Ile32Phe) n.3797A>T | dbSNP |
2 | g.29227048T>C | CA346468023 | ALK | c.2941A>G (p.Ile981Val) c.107A>G c.1810A>G (p.Ile604Val) c.94A>G (p.Ile32Val) n.3797A>G | |
2 | g.29227048T>G | CA346468026 | ALK | c.2941A>C (p.Ile981Leu) c.107A>C c.1810A>C (p.Ile604Leu) c.94A>C (p.Ile32Leu) n.3797A>C | |
2 | g.29227049A>C | CA346468030 | ALK | c.2940T>G (p.Asn980Lys) c.106T>G c.1809T>G (p.Asn603Lys) c.93T>G (p.Asn31Lys) n.3796T>G | dbSNP |
2 | g.29227049A>G | CA425436009 | ALK | c.2940T>C (p.Asn980=) c.106T>C c.1809T>C (p.Asn603=) c.93T>C (p.Asn31=) n.3796T>C | ClinVar |
2 | g.29227049A>T | CA346468028 | ALK | c.2940T>A (p.Asn980Lys) c.106T>A c.1809T>A (p.Asn603Lys) c.93T>A (p.Asn31Lys) n.3796T>A | dbSNP |
2 | g.29227050T>A | CA346468032 | ALK | c.2939A>T (p.Asn980Ile) c.105A>T c.1808A>T (p.Asn603Ile) c.92A>T (p.Asn31Ile) n.3795A>T | |
2 | g.29227050T>C | CA346468034 | ALK | c.2939A>G (p.Asn980Ser) c.105A>G c.1808A>G (p.Asn603Ser) c.92A>G (p.Asn31Ser) n.3795A>G | |
2 | g.29227050T>G | CA346468035 | ALK | c.2939A>C (p.Asn980Thr) c.105A>C c.1808A>C (p.Asn603Thr) c.92A>C (p.Asn31Thr) n.3795A>C | dbSNP |
2 | g.29227051T>A | CA346468038 | ALK | c.2938A>T (p.Asn980Tyr) c.104A>T c.1807A>T (p.Asn603Tyr) c.91A>T (p.Asn31Tyr) n.3794A>T | |
2 | g.29227051T>C | CA346468040 | ALK | c.2938A>G (p.Asn980Asp) c.104A>G c.1807A>G (p.Asn603Asp) c.91A>G (p.Asn31Asp) n.3794A>G | |
2 | g.29227051T>G | CA346468042 | ALK | c.2938A>C (p.Asn980His) c.104A>C c.1807A>C (p.Asn603His) c.91A>C (p.Asn31His) n.3794A>C | |
2 | g.29227052C>A | CA425436012 | ALK | c.2937G>T (p.Val979=) c.103G>T c.1806G>T (p.Val602=) c.90G>T (p.Val30=) n.3793G>T | dbSNP |
2 | g.29227052C>G | CA425436013 | ALK | c.2937G>C (p.Val979=) c.103G>C c.1806G>C (p.Val602=) c.90G>C (p.Val30=) n.3793G>C | dbSNP |
2 | g.29227052C>T | CA425436014 | ALK | c.2937G>A (p.Val979=) c.103G>A c.1806G>A (p.Val602=) c.90G>A (p.Val30=) n.3793G>A | dbSNP gnomAD v4 |
2 | g.29227053A>C | CA346468045 | ALK | c.2936T>G (p.Val979Gly) c.102T>G c.1805T>G (p.Val602Gly) c.89T>G (p.Val30Gly) n.3792T>G | dbSNP |
2 | g.29227053A>G | CA346468049 | ALK | c.2936T>C (p.Val979Ala) c.102T>C c.1805T>C (p.Val602Ala) c.89T>C (p.Val30Ala) n.3792T>C | dbSNP |
2 | g.29227053A>T | CA346468047 | ALK | c.2936T>A (p.Val979Glu) c.102T>A c.1805T>A (p.Val602Glu) c.89T>A (p.Val30Glu) n.3792T>A | dbSNP |
2 | g.29227054C>A | CA346468051 | ALK | c.2935G>T (p.Val979Leu) c.101G>T c.1804G>T (p.Val602Leu) c.88G>T (p.Val30Leu) n.3791G>T | dbSNP |
2 | g.29227054C>G | CA346468054 | ALK | c.2935G>C (p.Val979Leu) c.101G>C c.1804G>C (p.Val602Leu) c.88G>C (p.Val30Leu) n.3791G>C | dbSNP |
2 | g.29227054C>T | CA346468059 | ALK | c.2935G>A (p.Val979Met) c.101G>A c.1804G>A (p.Val602Met) c.88G>A (p.Val30Met) n.3791G>A | ClinVar dbSNP |
2 | g.29227055T>A | CA346468061 | ALK | c.2934A>T (p.Glu978Asp) c.100A>T c.1803A>T (p.Glu601Asp) c.87A>T (p.Glu29Asp) n.3790A>T | dbSNP |
2 | g.29227055T>C | CA425436016 | ALK | c.2934A>G (p.Glu978=) c.100A>G c.1803A>G (p.Glu601=) c.87A>G (p.Glu29=) n.3790A>G | |
2 | g.29227055T>G | CA346468062 | ALK | c.2934A>C (p.Glu978Asp) c.100A>C c.1803A>C (p.Glu601Asp) c.87A>C (p.Glu29Asp) n.3790A>C | |
2 | g.29227056del | CA2658460458 | ALK | c.2934del (p.Val979Ter) c.100del c.1803del (p.Val602Ter) c.87del (p.Val30Ter) n.3790del | gnomAD v4 |
2 | g.29227056T>A | CA346468064 | ALK | c.2933A>T (p.Glu978Val) c.99A>T c.1802A>T (p.Glu601Val) c.86A>T (p.Glu29Val) n.3789A>T | |
2 | g.29227056T>C | CA346468066 | ALK | c.2933A>G (p.Glu978Gly) c.99A>G c.1802A>G (p.Glu601Gly) c.86A>G (p.Glu29Gly) n.3789A>G | gnomAD v4 |
2 | g.29227056T>G | CA346468067 | ALK | c.2933A>C (p.Glu978Ala) c.99A>C c.1802A>C (p.Glu601Ala) c.86A>C (p.Glu29Ala) n.3789A>C | |
2 | g.29227057C>A | CA346468069 | ALK | c.2932G>T (p.Glu978Ter) c.98G>T c.1801G>T (p.Glu601Ter) c.85G>T (p.Glu29Ter) n.3788G>T | dbSNP gnomAD v4 |
2 | g.29227057C>G | CA346468072 | ALK | c.2932G>C (p.Glu978Gln) c.98G>C c.1801G>C (p.Glu601Gln) c.85G>C (p.Glu29Gln) n.3788G>C | dbSNP |
2 | g.29227057C>T | CA346468074 | ALK | c.2932G>A (p.Glu978Lys) c.98G>A c.1801G>A (p.Glu601Lys) c.85G>A (p.Glu29Lys) n.3788G>A | dbSNP |
2 | g.29227060del | CA2658460461 | ALK | c.2932del (p.Glu978LysfsTer2) c.98del c.1801del (p.Glu601LysfsTer2) c.85del (p.Glu29LysfsTer2) n.3788del | gnomAD v4 |
2 | g.29227058C>A | CA425436021 | ALK | c.2931G>T (p.Gly977=) c.97G>T c.1800G>T (p.Gly600=) c.84G>T (p.Gly28=) n.3787G>T | dbSNP |
2 | g.29227058C>G | CA425436022 | ALK | c.2931G>C (p.Gly977=) c.97G>C c.1800G>C (p.Gly600=) c.84G>C (p.Gly28=) n.3787G>C | |
2 | g.29227058C>T | CA425436023 | ALK | c.2931G>A (p.Gly977=) c.97G>A c.1800G>A (p.Gly600=) c.84G>A (p.Gly28=) n.3787G>A | dbSNP |
2 | g.29227059C>A | CA346468077 | ALK | c.2930G>T (p.Gly977Val) c.96G>T c.1799G>T (p.Gly600Val) c.83G>T (p.Gly28Val) n.3786G>T | dbSNP |
2 | g.29227059C>G | CA346468082 | ALK | c.2930G>C (p.Gly977Ala) c.96G>C c.1799G>C (p.Gly600Ala) c.83G>C (p.Gly28Ala) n.3786G>C | dbSNP |
2 | g.29227059C>T | CA346468079 | ALK | c.2930G>A (p.Gly977Glu) c.96G>A c.1799G>A (p.Gly600Glu) c.83G>A (p.Gly28Glu) n.3786G>A | dbSNP COSMIC |
2 | g.29227060C>A | CA346468085 | ALK | c.2929G>T (p.Gly977Trp) c.95G>T c.1798G>T (p.Gly600Trp) c.82G>T (p.Gly28Trp) n.3785G>T | ClinVar dbSNP |
2 | g.29227060C= | CA1241092887 | ALK | c.2929G= (p.Gly977=) c.95G= c.1798G= (p.Gly600=) c.82G= (p.Gly28=) n.3785G= | |
2 | g.29227060C>G | CA346468088 | ALK | c.2929G>C (p.Gly977Arg) c.95G>C c.1798G>C (p.Gly600Arg) c.82G>C (p.Gly28Arg) n.3785G>C | dbSNP |
2 | g.29227060C>T | CA1594121 | ALK | c.2929G>A (p.Gly977Arg) c.95G>A c.1798G>A (p.Gly600Arg) c.82G>A (p.Gly28Arg) n.3785G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29227061G>A | CA1594122 | ALK | c.2928C>T (p.His976=) c.94C>T c.1797C>T (p.His599=) c.81C>T (p.His27=) n.3784C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.29227061G>C | CA346468094 | ALK | c.2928C>G (p.His976Gln) c.94C>G c.1797C>G (p.His599Gln) c.81C>G (p.His27Gln) n.3784C>G | dbSNP |
2 | g.29227061G= | CA1241092888 | ALK | c.2928C= (p.His976=) c.94C= c.1797C= (p.His599=) c.81C= (p.His27=) n.3784C= | |
2 | g.29227061G>T | CA346468095 | ALK | c.2928C>A (p.His976Gln) c.94C>A c.1797C>A (p.His599Gln) c.81C>A (p.His27Gln) n.3784C>A | ClinVar |
2 | g.29227062T>A | CA346468097 | ALK | c.2927A>T (p.His976Leu) c.93A>T c.1796A>T (p.His599Leu) c.80A>T (p.His27Leu) n.3783A>T | |
2 | g.29227062T>C | CA346468098 | ALK | c.2927A>G (p.His976Arg) c.93A>G c.1796A>G (p.His599Arg) c.80A>G (p.His27Arg) n.3783A>G | |
2 | g.29227062T>G | CA346468101 | ALK | c.2927A>C (p.His976Pro) c.93A>C c.1796A>C (p.His599Pro) c.80A>C (p.His27Pro) n.3783A>C | gnomAD v4 |
2 | g.29227063G>A | CA346468104 | ALK | c.2926C>T (p.His976Tyr) c.92C>T c.1795C>T (p.His599Tyr) c.79C>T (p.His27Tyr) n.3782C>T | ClinVar dbSNP |
2 | g.29227063G>C | CA346468106 | ALK | c.2926C>G (p.His976Asp) c.92C>G c.1795C>G (p.His599Asp) c.79C>G (p.His27Asp) n.3782C>G | dbSNP |
2 | g.29227063G= | CA1241092889 | ALK | c.2926C= (p.His976=) c.92C= c.1795C= (p.His599=) c.79C= (p.His27=) n.3782C= | |
2 | g.29227063G>T | CA346468108 | ALK | c.2926C>A (p.His976Asn) c.92C>A c.1795C>A (p.His599Asn) c.79C>A (p.His27Asn) n.3782C>A | |
2 | g.29227064G>A | CA425436029 | ALK | c.2925C>T (p.Gly975=) c.91C>T c.1794C>T (p.Gly598=) c.78C>T (p.Gly26=) n.3781C>T | |
2 | g.29227064G>C | CA425436030 | ALK | c.2925C>G (p.Gly975=) c.91C>G c.1794C>G (p.Gly598=) c.78C>G (p.Gly26=) n.3781C>G | |
2 | g.29227064G>T | CA425436031 | ALK | c.2925C>A (p.Gly975=) c.91C>A c.1794C>A (p.Gly598=) c.78C>A (p.Gly26=) n.3781C>A | |
2 | g.29227065C>A | CA346468115 | ALK | c.2924G>T (p.Gly975Val) c.90G>T c.1793G>T (p.Gly598Val) c.77G>T (p.Gly26Val) n.3780G>T | ClinVar dbSNP gnomAD v4 |
2 | g.29227065C= | CA1241092890 | ALK | c.2924G= (p.Gly975=) c.90G= c.1793G= (p.Gly598=) c.77G= (p.Gly26=) n.3780G= | |
2 | g.29227065C>G | CA346468110 | ALK | c.2924G>C (p.Gly975Ala) c.90G>C c.1793G>C (p.Gly598Ala) c.77G>C (p.Gly26Ala) n.3780G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.29227065C>T | CA346468113 | ALK | c.2924G>A (p.Gly975Asp) c.90G>A c.1793G>A (p.Gly598Asp) c.77G>A (p.Gly26Asp) n.3780G>A | dbSNP gnomAD v4 |
2 | g.29227066C>A | CA346468117 | ALK | c.2923G>T (p.Gly975Cys) c.89G>T c.1792G>T (p.Gly598Cys) c.76G>T (p.Gly26Cys) n.3779G>T | dbSNP |
2 | g.29227066C>G | CA346468121 | ALK | c.2923G>C (p.Gly975Arg) c.89G>C c.1792G>C (p.Gly598Arg) c.76G>C (p.Gly26Arg) n.3779G>C | dbSNP |
2 | g.29227066C>T | CA346468123 | ALK | c.2923G>A (p.Gly975Ser) c.89G>A c.1792G>A (p.Gly598Ser) c.76G>A (p.Gly26Ser) n.3779G>A | dbSNP |
2 | g.29227067T>A | CA346468124 | ALK | c.2922A>T (p.Glu974Asp) c.88A>T c.1791A>T (p.Glu597Asp) c.75A>T (p.Glu25Asp) n.3778A>T | |
2 | g.29227067T>C | CA425436034 | ALK | c.2922A>G (p.Glu974=) c.88A>G c.1791A>G (p.Glu597=) c.75A>G (p.Glu25=) n.3778A>G | dbSNP |
2 | g.29227067T>G | CA346468125 | ALK | c.2922A>C (p.Glu974Asp) c.88A>C c.1791A>C (p.Glu597Asp) c.75A>C (p.Glu25Asp) n.3778A>C | ClinVar |
2 | g.29227068del | CA2658460478 | ALK | c.2922del (p.Gly975AlafsTer5) c.88del c.1791del (p.Gly598AlafsTer5) c.75del (p.Gly26AlafsTer5) n.3778del | gnomAD v4 |
2 | g.29227068T>A | CA346468129 | ALK | c.2921A>T (p.Glu974Val) c.87A>T c.1790A>T (p.Glu597Val) c.74A>T (p.Glu25Val) n.3777A>T | |
2 | g.29227068T>C | CA346468130 | ALK | c.2921A>G (p.Glu974Gly) c.87A>G c.1790A>G (p.Glu597Gly) c.74A>G (p.Glu25Gly) n.3777A>G | |
2 | g.29227068T>G | CA346468132 | ALK | c.2921A>C (p.Glu974Ala) c.87A>C c.1790A>C (p.Glu597Ala) c.74A>C (p.Glu25Ala) n.3777A>C | |
2 | g.29227069C>A | CA346468133 | ALK | c.2920G>T (p.Glu974Ter) c.86G>T c.1789G>T (p.Glu597Ter) c.73G>T (p.Glu25Ter) n.3776G>T | dbSNP |
2 | g.29227069C>G | CA346468135 | ALK | c.2920G>C (p.Glu974Gln) c.86G>C c.1789G>C (p.Glu597Gln) c.73G>C (p.Glu25Gln) n.3776G>C | dbSNP |
2 | g.29227069C>T | CA346468136 | ALK | c.2920G>A (p.Glu974Lys) c.86G>A c.1789G>A (p.Glu597Lys) c.73G>A (p.Glu25Lys) n.3776G>A | dbSNP |
2 | g.29227070C>A | CA346468139 | ALK | c.2919G>T (p.Met973Ile) c.85G>T c.1788G>T (p.Met596Ile) c.72G>T (p.Met24Ile) n.3775G>T | dbSNP |
2 | g.29227070C>G | CA346468138 | ALK | c.2919G>C (p.Met973Ile) c.85G>C c.1788G>C (p.Met596Ile) c.72G>C (p.Met24Ile) n.3775G>C | |
2 | g.29227070C>T | CA346468137 | ALK | c.2919G>A (p.Met973Ile) c.85G>A c.1788G>A (p.Met596Ile) c.72G>A (p.Met24Ile) n.3775G>A | ClinVar dbSNP |
2 | g.29227071A>C | CA346468141 | ALK | c.2918T>G (p.Met973Arg) c.84T>G c.1787T>G (p.Met596Arg) c.71T>G (p.Met24Arg) n.3774T>G | dbSNP |
2 | g.29227071A>G | CA346468140 | ALK | c.2918T>C (p.Met973Thr) c.84T>C c.1787T>C (p.Met596Thr) c.71T>C (p.Met24Thr) n.3774T>C | |
2 | g.29227071A>T | CA346468144 | ALK | c.2918T>A (p.Met973Lys) c.84T>A c.1787T>A (p.Met596Lys) c.71T>A (p.Met24Lys) n.3774T>A | dbSNP |
2 | g.29227072T>A | CA346468146 | ALK | c.2917A>T (p.Met973Leu) c.83A>T c.1786A>T (p.Met596Leu) c.70A>T (p.Met24Leu) n.3773A>T | |
2 | g.29227072T>C | CA346468148 | ALK | c.2917A>G (p.Met973Val) c.83A>G c.1786A>G (p.Met596Val) c.70A>G (p.Met24Val) n.3773A>G | ClinVar dbSNP |
2 | g.29227072T>G | CA346468150 | ALK | c.2917A>C (p.Met973Leu) c.83A>C c.1786A>C (p.Met596Leu) c.70A>C (p.Met24Leu) n.3773A>C | |
2 | g.29227072T= | CA1241092891 | ALK | c.2917A= (p.Met973=) c.83A= c.1786A= (p.Met596=) c.70A= (p.Met24=) n.3773A= | |
2 | g.29227073C>A | CA425436037 | ALK | c.2916G>T (p.Val972=) c.82G>T c.1785G>T (p.Val595=) c.69G>T (p.Val23=) n.3772G>T | dbSNP |
2 | g.29227073C>G | CA425436038 | ALK | c.2916G>C (p.Val972=) c.82G>C c.1785G>C (p.Val595=) c.69G>C (p.Val23=) n.3772G>C | dbSNP |
2 | g.29227073C>T | CA425436040 | ALK | c.2916G>A (p.Val972=) c.82G>A c.1785G>A (p.Val595=) c.69G>A (p.Val23=) n.3772G>A | dbSNP gnomAD v4 |
2 | g.29227074A= | CA1241092892 | ALK | c.2915T= (p.Val972=) c.81T= c.1784T= (p.Val595=) c.68T= (p.Val23=) n.3771T= | |
2 | g.29227074A>C | CA346468153 | ALK | c.2915T>G (p.Val972Gly) c.81T>G c.1784T>G (p.Val595Gly) c.68T>G (p.Val23Gly) n.3771T>G | |
2 | g.29227074A>G | CA346468155 | ALK | c.2915T>C (p.Val972Ala) c.81T>C c.1784T>C (p.Val595Ala) c.68T>C (p.Val23Ala) n.3771T>C | ClinVar dbSNP gnomAD v4 |
2 | g.29227074A>T | CA346468158 | ALK | c.2915T>A (p.Val972Glu) c.81T>A c.1784T>A (p.Val595Glu) c.68T>A (p.Val23Glu) n.3771T>A | dbSNP |
2 | g.29227075C>A | CA346468160 | ALK | c.2915-1G>T (n.2915-1G>T) c.81-1G>T c.1784-1G>T (n.1784-1G>T) c.68-1G>T (n.68-1G>T) n.3771-1G>T | dbSNP |
2 | g.29227075C>G | CA346468161 | ALK | c.2915-1G>C (n.2915-1G>C) c.81-1G>C c.1784-1G>C (n.1784-1G>C) c.68-1G>C (n.68-1G>C) n.3771-1G>C | dbSNP |
2 | g.29227075C>T | CA346468165 | ALK | c.2915-1G>A (n.2915-1G>A) c.81-1G>A c.1784-1G>A (n.1784-1G>A) c.68-1G>A (n.68-1G>A) n.3771-1G>A | gnomAD v4 |