UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.91724148G>A | CA466339034 | ROR2 | c.2346C>T (p.Ser782=) c.1920+6C>T (n.1920+6C>T) n.2814C>T c.1926C>T (p.Ser642=) c.1143C>T (p.Ser381=) c.2337C>T (p.Ser779=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724148G>C | CA373794636 | ROR2 | c.2346C>G (p.Ser782Arg) c.1920+6C>G (n.1920+6C>G) n.2814C>G c.1926C>G (p.Ser642Arg) c.1143C>G (p.Ser381Arg) c.2337C>G (p.Ser779Arg) | |
| 9 | g.91724148G= | CA1863922223 | ROR2 | c.2346C= (p.Ser782=) c.1920+6C= (n.1920+6C=) n.2814C= c.1926C= (p.Ser642=) c.1143C= (p.Ser381=) c.2337C= (p.Ser779=) | |
| 9 | g.91724148G>T | CA373794637 | ROR2 | c.2346C>A (p.Ser782Arg) c.1920+6C>A (n.1920+6C>A) n.2814C>A c.1926C>A (p.Ser642Arg) c.1143C>A (p.Ser381Arg) c.2337C>A (p.Ser779Arg) | |
| 9 | g.91724149C>A | CA373794638 | ROR2 | c.2345G>T (p.Ser782Ile) c.1920+5G>T (n.1920+5G>T) n.2813G>T c.1925G>T (p.Ser642Ile) c.1142G>T (p.Ser381Ile) c.2336G>T (p.Ser779Ile) | |
| 9 | g.91724149C>G | CA373794640 | ROR2 | c.2345G>C (p.Ser782Thr) c.1920+5G>C (n.1920+5G>C) n.2813G>C c.1925G>C (p.Ser642Thr) c.1142G>C (p.Ser381Thr) c.2336G>C (p.Ser779Thr) | |
| 9 | g.91724149C>T | CA373794641 | ROR2 | c.2345G>A (p.Ser782Asn) c.1920+5G>A (n.1920+5G>A) n.2813G>A c.1925G>A (p.Ser642Asn) c.1142G>A (p.Ser381Asn) c.2336G>A (p.Ser779Asn) | |
| 9 | g.91724150T>A | CA373794642 | ROR2 | c.2344A>T (p.Ser782Cys) c.1920+4A>T (n.1920+4A>T) n.2812A>T c.1924A>T (p.Ser642Cys) c.1141A>T (p.Ser381Cys) c.2335A>T (p.Ser779Cys) | |
| 9 | g.91724150T>C | CA373794643 | ROR2 | c.2344A>G (p.Ser782Gly) c.1920+4A>G (n.1920+4A>G) n.2812A>G c.1924A>G (p.Ser642Gly) c.1141A>G (p.Ser381Gly) c.2335A>G (p.Ser779Gly) | |
| 9 | g.91724150T>G | CA373794645 | ROR2 | c.2344A>C (p.Ser782Arg) c.1920+4A>C (n.1920+4A>C) n.2812A>C c.1924A>C (p.Ser642Arg) c.1141A>C (p.Ser381Arg) c.2335A>C (p.Ser779Arg) | |
| 9 | g.91724151C>A | CA466339037 | ROR2 | c.2343G>T (p.Val781=) c.1920+3G>T (n.1920+3G>T) n.2811G>T c.1923G>T (p.Val641=) c.1140G>T (p.Val380=) c.2334G>T (p.Val778=) | gnomAD v4 |
| 9 | g.91724151C>G | CA466339038 | ROR2 | c.2343G>C (p.Val781=) c.1920+3G>C (n.1920+3G>C) n.2811G>C c.1923G>C (p.Val641=) c.1140G>C (p.Val380=) c.2334G>C (p.Val778=) | |
| 9 | g.91724151C>T | CA466339039 | ROR2 | c.2343G>A (p.Val781=) c.1920+3G>A (n.1920+3G>A) n.2811G>A c.1923G>A (p.Val641=) c.1140G>A (p.Val380=) c.2334G>A (p.Val778=) | COSMIC |
| 9 | g.91724153_91724154del | CA2690632290 | ROR2 | c.2342_2343del (p.Val781GlufsTer?) c.1920+2_1920+3del n.2810_2811del c.1922_1923del (p.Val641GlufsTer?) c.1139_1140del (p.Val380GlufsTer?) c.2333_2334del (p.Val778GlufsTer?) | gnomAD v4 |
| 9 | g.91724152A>C | CA373794646 | ROR2 | c.2342T>G (p.Val781Gly) c.1920+2T>G (n.1920+2T>G) n.2810T>G c.1922T>G (p.Val641Gly) c.1139T>G (p.Val380Gly) c.2333T>G (p.Val778Gly) | |
| 9 | g.91724152A>G | CA373794648 | ROR2 | c.2342T>C (p.Val781Ala) c.1920+2T>C (n.1920+2T>C) n.2810T>C c.1922T>C (p.Val641Ala) c.1139T>C (p.Val380Ala) c.2333T>C (p.Val778Ala) | |
| 9 | g.91724152A>T | CA373794647 | ROR2 | c.2342T>A (p.Val781Glu) c.1920+2T>A (n.1920+2T>A) n.2810T>A c.1922T>A (p.Val641Glu) c.1139T>A (p.Val380Glu) c.2333T>A (p.Val778Glu) | |
| 9 | g.91724153C>A | CA373794650 | ROR2 | c.2341G>T (p.Val781Leu) c.1920+1G>T (n.1920+1G>T) n.2809G>T c.1921G>T (p.Val641Leu) c.1138G>T (p.Val380Leu) c.2332G>T (p.Val778Leu) | |
| 9 | g.91724153C= | CA1863922226 | ROR2 | c.2341G= (p.Val781=) c.1920+1G= (n.1920+1G=) n.2809G= c.1921G= (p.Val641=) c.1138G= (p.Val380=) c.2332G= (p.Val778=) | |
| 9 | g.91724153C>G | CA373794655 | ROR2 | c.2341G>C (p.Val781Leu) c.1920+1G>C (n.1920+1G>C) n.2809G>C c.1921G>C (p.Val641Leu) c.1138G>C (p.Val380Leu) c.2332G>C (p.Val778Leu) | |
| 9 | g.91724153C>T | CA5120420 | ROR2 | c.2341G>A (p.Val781Met) c.1920+1G>A (n.1920+1G>A) n.2809G>A c.1921G>A (p.Val641Met) c.1138G>A (p.Val380Met) c.2332G>A (p.Val778Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724154A>C | CA373794657 | ROR2 | c.2340T>G (p.Asn780Lys) c.1920T>G (p.Asn640Lys) n.2808T>G c.1137T>G (p.Asn379Lys) c.2331T>G (p.Asn777Lys) | |
| 9 | g.91724154A>G | CA466339040 | ROR2 | c.2340T>C (p.Asn780=) c.1920T>C (p.Asn640=) n.2808T>C c.1137T>C (p.Asn379=) c.2331T>C (p.Asn777=) | |
| 9 | g.91724154A>T | CA373794659 | ROR2 | c.2340T>A (p.Asn780Lys) c.1920T>A (p.Asn640Lys) n.2808T>A c.1137T>A (p.Asn379Lys) c.2331T>A (p.Asn777Lys) | |
| 9 | g.91724155T>A | CA373794661 | ROR2 | c.2339A>T (p.Asn780Ile) c.1919A>T (p.Asn640Ile) n.2807A>T c.1136A>T (p.Asn379Ile) c.2330A>T (p.Asn777Ile) | |
| 9 | g.91724155T>C | CA373794662 | ROR2 | c.2339A>G (p.Asn780Ser) c.1919A>G (p.Asn640Ser) n.2807A>G c.1136A>G (p.Asn379Ser) c.2330A>G (p.Asn777Ser) | dbSNP |
| 9 | g.91724155T>G | CA373794665 | ROR2 | c.2339A>C (p.Asn780Thr) c.1919A>C (p.Asn640Thr) n.2807A>C c.1136A>C (p.Asn379Thr) c.2330A>C (p.Asn777Thr) | |
| 9 | g.91724155T= | CA1863922230 | ROR2 | c.2339A= (p.Asn780=) c.1919A= (p.Asn640=) n.2807A= c.1136A= (p.Asn379=) c.2330A= (p.Asn777=) | |
| 9 | g.91724156T>A | CA373794666 | ROR2 | c.2338A>T (p.Asn780Tyr) c.1918A>T (p.Asn640Tyr) n.2806A>T c.1135A>T (p.Asn379Tyr) c.2329A>T (p.Asn777Tyr) | |
| 9 | g.91724156T>C | CA373794668 | ROR2 | c.2338A>G (p.Asn780Asp) c.1918A>G (p.Asn640Asp) n.2806A>G c.1135A>G (p.Asn379Asp) c.2329A>G (p.Asn777Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724156T>G | CA373794667 | ROR2 | c.2338A>C (p.Asn780His) c.1918A>C (p.Asn640His) n.2806A>C c.1135A>C (p.Asn379His) c.2329A>C (p.Asn777His) | |
| 9 | g.91724156T= | CA1863922232 | ROR2 | c.2338A= (p.Asn780=) c.1918A= (p.Asn640=) n.2806A= c.1135A= (p.Asn379=) c.2329A= (p.Asn777=) | |
| 9 | g.91724157G>A | CA466339041 | ROR2 | c.2337C>T (p.Ser779=) c.1917C>T (p.Ser639=) n.2805C>T c.1134C>T (p.Ser378=) c.2328C>T (p.Ser776=) | gnomAD v4 |
| 9 | g.91724157G>C | CA373794672 | ROR2 | c.2337C>G (p.Ser779Arg) c.1917C>G (p.Ser639Arg) n.2805C>G c.1134C>G (p.Ser378Arg) c.2328C>G (p.Ser776Arg) | gnomAD v4 |
| 9 | g.91724157G>T | CA373794673 | ROR2 | c.2337C>A (p.Ser779Arg) c.1917C>A (p.Ser639Arg) n.2805C>A c.1134C>A (p.Ser378Arg) c.2328C>A (p.Ser776Arg) | gnomAD v4 COSMIC |
| 9 | g.91724158C>A | CA373794675 | ROR2 | c.2336G>T (p.Ser779Ile) c.1916G>T (p.Ser639Ile) n.2804G>T c.1133G>T (p.Ser378Ile) c.2327G>T (p.Ser776Ile) | |
| 9 | g.91724158C>G | CA373794677 | ROR2 | c.2336G>C (p.Ser779Thr) c.1916G>C (p.Ser639Thr) n.2804G>C c.1133G>C (p.Ser378Thr) c.2327G>C (p.Ser776Thr) | |
| 9 | g.91724158C>T | CA373794679 | ROR2 | c.2336G>A (p.Ser779Asn) c.1916G>A (p.Ser639Asn) n.2804G>A c.1133G>A (p.Ser378Asn) c.2327G>A (p.Ser776Asn) | gnomAD v4 |
| 9 | g.91724159T>A | CA373794681 | ROR2 | c.2335A>T (p.Ser779Cys) c.1915A>T (p.Ser639Cys) n.2803A>T c.1132A>T (p.Ser378Cys) c.2326A>T (p.Ser776Cys) | |
| 9 | g.91724159T>C | CA373794685 | ROR2 | c.2335A>G (p.Ser779Gly) c.1915A>G (p.Ser639Gly) n.2803A>G c.1132A>G (p.Ser378Gly) c.2326A>G (p.Ser776Gly) | COSMIC |
| 9 | g.91724159T>G | CA373794683 | ROR2 | c.2335A>C (p.Ser779Arg) c.1915A>C (p.Ser639Arg) n.2803A>C c.1132A>C (p.Ser378Arg) c.2326A>C (p.Ser776Arg) | |
| 9 | g.91724160C>A | CA466339046 | ROR2 | c.2334G>T (p.Val778=) c.1914G>T (p.Val638=) n.2802G>T c.1131G>T (p.Val377=) c.2325G>T (p.Val775=) | |
| 9 | g.91724160C>G | CA466339047 | ROR2 | c.2334G>C (p.Val778=) c.1914G>C (p.Val638=) n.2802G>C c.1131G>C (p.Val377=) c.2325G>C (p.Val775=) | |
| 9 | g.91724160C>T | CA466339048 | ROR2 | c.2334G>A (p.Val778=) c.1914G>A (p.Val638=) n.2802G>A c.1131G>A (p.Val377=) c.2325G>A (p.Val775=) | |
| 9 | g.91724161A= | CA1863922234 | ROR2 | c.2333T= (p.Val778=) c.1913T= (p.Val638=) n.2801T= c.1130T= (p.Val377=) c.2324T= (p.Val775=) | |
| 9 | g.91724161A>C | CA373794686 | ROR2 | c.2333T>G (p.Val778Gly) c.1913T>G (p.Val638Gly) n.2801T>G c.1130T>G (p.Val377Gly) c.2324T>G (p.Val775Gly) | |
| 9 | g.91724161A>G | CA373794688 | ROR2 | c.2333T>C (p.Val778Ala) c.1913T>C (p.Val638Ala) n.2801T>C c.1130T>C (p.Val377Ala) c.2324T>C (p.Val775Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724161A>T | CA373794690 | ROR2 | c.2333T>A (p.Val778Glu) c.1913T>A (p.Val638Glu) n.2801T>A c.1130T>A (p.Val377Glu) c.2324T>A (p.Val775Glu) | |
| 9 | g.91724162C>A | CA373794691 | ROR2 | c.2332G>T (p.Val778Leu) c.1912G>T (p.Val638Leu) n.2800G>T c.1129G>T (p.Val377Leu) c.2323G>T (p.Val775Leu) | |
| 9 | g.91724162C>G | CA373794692 | ROR2 | c.2332G>C (p.Val778Leu) c.1912G>C (p.Val638Leu) n.2800G>C c.1129G>C (p.Val377Leu) c.2323G>C (p.Val775Leu) | |
| 9 | g.91724162C>T | CA373794694 | ROR2 | c.2332G>A (p.Val778Met) c.1912G>A (p.Val638Met) n.2800G>A c.1129G>A (p.Val377Met) c.2323G>A (p.Val775Met) | |
| 9 | g.91724163T>A | CA466339051 | ROR2 | c.2331A>T (p.Pro777=) c.1911A>T (p.Pro637=) n.2799A>T c.1128A>T (p.Pro376=) c.2322A>T (p.Pro774=) | |
| 9 | g.91724163T>C | CA466339053 | ROR2 | c.2331A>G (p.Pro777=) c.1911A>G (p.Pro637=) n.2799A>G c.1128A>G (p.Pro376=) c.2322A>G (p.Pro774=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724163T>G | CA466339055 | ROR2 | c.2331A>C (p.Pro777=) c.1911A>C (p.Pro637=) n.2799A>C c.1128A>C (p.Pro376=) c.2322A>C (p.Pro774=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724163T= | CA1863922236 | ROR2 | c.2331A= (p.Pro777=) c.1911A= (p.Pro637=) n.2799A= c.1128A= (p.Pro376=) c.2322A= (p.Pro774=) | |
| 9 | g.91724164G>A | CA373794699 | ROR2 | c.2330C>T (p.Pro777Leu) c.1910C>T (p.Pro637Leu) n.2798C>T c.1127C>T (p.Pro376Leu) c.2321C>T (p.Pro774Leu) | gnomAD v4 |
| 9 | g.91724164G>C | CA373794701 | ROR2 | c.2330C>G (p.Pro777Arg) c.1910C>G (p.Pro637Arg) n.2798C>G c.1127C>G (p.Pro376Arg) c.2321C>G (p.Pro774Arg) | |
| 9 | g.91724164G>T | CA373794703 | ROR2 | c.2330C>A (p.Pro777Gln) c.1910C>A (p.Pro637Gln) n.2798C>A c.1127C>A (p.Pro376Gln) c.2321C>A (p.Pro774Gln) | gnomAD v4 |
| 9 | g.91724165G>A | CA373794704 | ROR2 | c.2329C>T (p.Pro777Ser) c.1909C>T (p.Pro637Ser) n.2797C>T c.1126C>T (p.Pro376Ser) c.2320C>T (p.Pro774Ser) | |
| 9 | g.91724165G>C | CA373794705 | ROR2 | c.2329C>G (p.Pro777Ala) c.1909C>G (p.Pro637Ala) n.2797C>G c.1126C>G (p.Pro376Ala) c.2320C>G (p.Pro774Ala) | |
| 9 | g.91724165G>T | CA373794707 | ROR2 | c.2329C>A (p.Pro777Thr) c.1909C>A (p.Pro637Thr) n.2797C>A c.1126C>A (p.Pro376Thr) c.2320C>A (p.Pro774Thr) | |
| 9 | g.91724166G>A | CA5120421 | ROR2 | c.2328C>T (p.Ser776=) c.1908C>T (p.Ser636=) n.2796C>T c.1125C>T (p.Ser375=) c.2319C>T (p.Ser773=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724166G>C | CA373794711 | ROR2 | c.2328C>G (p.Ser776Arg) c.1908C>G (p.Ser636Arg) n.2796C>G c.1125C>G (p.Ser375Arg) c.2319C>G (p.Ser773Arg) | |
| 9 | g.91724166G= | CA1863922238 | ROR2 | c.2328C= (p.Ser776=) c.1908C= (p.Ser636=) n.2796C= c.1125C= (p.Ser375=) c.2319C= (p.Ser773=) | |
| 9 | g.91724166G>T | CA373794710 | ROR2 | c.2328C>A (p.Ser776Arg) c.1908C>A (p.Ser636Arg) n.2796C>A c.1125C>A (p.Ser375Arg) c.2319C>A (p.Ser773Arg) | |
| 9 | g.91724167C>A | CA373794713 | ROR2 | c.2327G>T (p.Ser776Ile) c.1907G>T (p.Ser636Ile) n.2795G>T c.1124G>T (p.Ser375Ile) c.2318G>T (p.Ser773Ile) | |
| 9 | g.91724167C>G | CA373794715 | ROR2 | c.2327G>C (p.Ser776Thr) c.1907G>C (p.Ser636Thr) n.2795G>C c.1124G>C (p.Ser375Thr) c.2318G>C (p.Ser773Thr) | gnomAD v4 |
| 9 | g.91724167C>T | CA373794717 | ROR2 | c.2327G>A (p.Ser776Asn) c.1907G>A (p.Ser636Asn) n.2795G>A c.1124G>A (p.Ser375Asn) c.2318G>A (p.Ser773Asn) | gnomAD v4 COSMIC |
| 9 | g.91724168T>A | CA373794719 | ROR2 | c.2326A>T (p.Ser776Cys) c.1906A>T (p.Ser636Cys) n.2794A>T c.1123A>T (p.Ser375Cys) c.2317A>T (p.Ser773Cys) | |
| 9 | g.91724168T>C | CA373794720 | ROR2 | c.2326A>G (p.Ser776Gly) c.1906A>G (p.Ser636Gly) n.2794A>G c.1123A>G (p.Ser375Gly) c.2317A>G (p.Ser773Gly) | |
| 9 | g.91724168T>G | CA373794721 | ROR2 | c.2326A>C (p.Ser776Arg) c.1906A>C (p.Ser636Arg) n.2794A>C c.1123A>C (p.Ser375Arg) c.2317A>C (p.Ser773Arg) | gnomAD v4 |
| 9 | g.91724169G>A | CA466339060 | ROR2 | c.2325C>T (p.Thr775=) c.1905C>T (p.Thr635=) n.2793C>T c.1122C>T (p.Thr374=) c.2316C>T (p.Thr772=) | |
| 9 | g.91724169G>C | CA466339061 | ROR2 | c.2325C>G (p.Thr775=) c.1905C>G (p.Thr635=) n.2793C>G c.1122C>G (p.Thr374=) c.2316C>G (p.Thr772=) | |
| 9 | g.91724169G>T | CA466339062 | ROR2 | c.2325C>A (p.Thr775=) c.1905C>A (p.Thr635=) n.2793C>A c.1122C>A (p.Thr374=) c.2316C>A (p.Thr772=) | gnomAD v4 |
| 9 | g.91724170G>A | CA373794726 | ROR2 | c.2324C>T (p.Thr775Ile) c.1904C>T (p.Thr635Ile) n.2792C>T c.1121C>T (p.Thr374Ile) c.2315C>T (p.Thr772Ile) | |
| 9 | g.91724170G>C | CA373794723 | ROR2 | c.2324C>G (p.Thr775Ser) c.1904C>G (p.Thr635Ser) n.2792C>G c.1121C>G (p.Thr374Ser) c.2315C>G (p.Thr772Ser) | ClinVar dbSNP |
| 9 | g.91724170G= | CA1863922242 | ROR2 | c.2324C= (p.Thr775=) c.1904C= (p.Thr635=) n.2792C= c.1121C= (p.Thr374=) c.2315C= (p.Thr772=) | |
| 9 | g.91724170G>T | CA373794725 | ROR2 | c.2324C>A (p.Thr775Asn) c.1904C>A (p.Thr635Asn) n.2792C>A c.1121C>A (p.Thr374Asn) c.2315C>A (p.Thr772Asn) | gnomAD v4 |
| 9 | g.91724171T>A | CA373794728 | ROR2 | c.2323A>T (p.Thr775Ser) c.1903A>T (p.Thr635Ser) n.2791A>T c.1120A>T (p.Thr374Ser) c.2314A>T (p.Thr772Ser) | |
| 9 | g.91724171T>C | CA373794735 | ROR2 | c.2323A>G (p.Thr775Ala) c.1903A>G (p.Thr635Ala) n.2791A>G c.1120A>G (p.Thr374Ala) c.2314A>G (p.Thr772Ala) | gnomAD v4 |
| 9 | g.91724171T>G | CA373794736 | ROR2 | c.2323A>C (p.Thr775Pro) c.1903A>C (p.Thr635Pro) n.2791A>C c.1120A>C (p.Thr374Pro) c.2314A>C (p.Thr772Pro) | |
| 9 | g.91724172G>A | CA195322310 | ROR2 | c.2322C>T (p.Ser774=) c.1902C>T (p.Ser634=) n.2790C>T c.1119C>T (p.Ser373=) c.2313C>T (p.Ser771=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724172G>C | CA373794738 | ROR2 | c.2322C>G (p.Ser774Arg) c.1902C>G (p.Ser634Arg) n.2790C>G c.1119C>G (p.Ser373Arg) c.2313C>G (p.Ser771Arg) | |
| 9 | g.91724172G= | CA1863922244 | ROR2 | c.2322C= (p.Ser774=) c.1902C= (p.Ser634=) n.2790C= c.1119C= (p.Ser373=) c.2313C= (p.Ser771=) | |
| 9 | g.91724172G>T | CA373794739 | ROR2 | c.2322C>A (p.Ser774Arg) c.1902C>A (p.Ser634Arg) n.2790C>A c.1119C>A (p.Ser373Arg) c.2313C>A (p.Ser771Arg) | gnomAD v4 |
| 9 | g.91724173C>A | CA373794740 | ROR2 | c.2321G>T (p.Ser774Ile) c.1901G>T (p.Ser634Ile) n.2789G>T c.1118G>T (p.Ser373Ile) c.2312G>T (p.Ser771Ile) | |
| 9 | g.91724173C>G | CA373794744 | ROR2 | c.2321G>C (p.Ser774Thr) c.1901G>C (p.Ser634Thr) n.2789G>C c.1118G>C (p.Ser373Thr) c.2312G>C (p.Ser771Thr) | |
| 9 | g.91724173C>T | CA373794741 | ROR2 | c.2321G>A (p.Ser774Asn) c.1901G>A (p.Ser634Asn) n.2789G>A c.1118G>A (p.Ser373Asn) c.2312G>A (p.Ser771Asn) | COSMIC |
| 9 | g.91724174T>A | CA373794746 | ROR2 | c.2320A>T (p.Ser774Cys) c.1900A>T (p.Ser634Cys) n.2788A>T c.1117A>T (p.Ser373Cys) c.2311A>T (p.Ser771Cys) | |
| 9 | g.91724174T>C | CA373794747 | ROR2 | c.2320A>G (p.Ser774Gly) c.1900A>G (p.Ser634Gly) n.2788A>G c.1117A>G (p.Ser373Gly) c.2311A>G (p.Ser771Gly) | |
| 9 | g.91724174T>G | CA373794748 | ROR2 | c.2320A>C (p.Ser774Arg) c.1900A>C (p.Ser634Arg) n.2788A>C c.1117A>C (p.Ser373Arg) c.2311A>C (p.Ser771Arg) | ClinVar |
| 9 | g.91724175C>A | CA466339066 | ROR2 | c.2319G>T (p.Leu773=) c.1899G>T (p.Leu633=) n.2787G>T c.1116G>T (p.Leu372=) c.2310G>T (p.Leu770=) | |
| 9 | g.91724175C>G | CA466339067 | ROR2 | c.2319G>C (p.Leu773=) c.1899G>C (p.Leu633=) n.2787G>C c.1116G>C (p.Leu372=) c.2310G>C (p.Leu770=) | |
| 9 | g.91724175C>T | CA466339068 | ROR2 | c.2319G>A (p.Leu773=) c.1899G>A (p.Leu633=) n.2787G>A c.1116G>A (p.Leu372=) c.2310G>A (p.Leu770=) | |
| 9 | g.91724176A= | CA1863922247 | ROR2 | c.2318T= (p.Leu773=) c.1898T= (p.Leu633=) n.2786T= c.1115T= (p.Leu372=) c.2309T= (p.Leu770=) | |
| 9 | g.91724176A>C | CA373794750 | ROR2 | c.2318T>G (p.Leu773Arg) c.1898T>G (p.Leu633Arg) n.2786T>G c.1115T>G (p.Leu372Arg) c.2309T>G (p.Leu770Arg) | |
| 9 | g.91724176A>G | CA373794753 | ROR2 | c.2318T>C (p.Leu773Pro) c.1898T>C (p.Leu633Pro) n.2786T>C c.1115T>C (p.Leu372Pro) c.2309T>C (p.Leu770Pro) | |
| 9 | g.91724176A>T | CA373794754 | ROR2 | c.2318T>A (p.Leu773Gln) c.1898T>A (p.Leu633Gln) n.2786T>A c.1115T>A (p.Leu372Gln) c.2309T>A (p.Leu770Gln) | |
| 9 | g.91724177G>A | CA466339069 | ROR2 | c.2317C>T (p.Leu773=) c.1897C>T (p.Leu633=) n.2785C>T c.1114C>T (p.Leu372=) c.2308C>T (p.Leu770=) | |
| 9 | g.91724177G>C | CA373794755 | ROR2 | c.2317C>G (p.Leu773Val) c.1897C>G (p.Leu633Val) n.2785C>G c.1114C>G (p.Leu372Val) c.2308C>G (p.Leu770Val) | gnomAD v4 |
| 9 | g.91724177G>T | CA373794756 | ROR2 | c.2317C>A (p.Leu773Met) c.1897C>A (p.Leu633Met) n.2785C>A c.1114C>A (p.Leu372Met) c.2308C>A (p.Leu770Met) | gnomAD v4 |
| 9 | g.91724179dup | CA589578515 | ROR2 | c.2317dup (p.Leu773ProfsTer?) c.1897dup (p.Leu633ProfsTer?) n.2785dup c.1114dup (p.Leu372ProfsTer?) c.2308dup (p.Leu770ProfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724178G>A | CA466339070 | ROR2 | c.2316C>T (p.Ser772=) c.1896C>T (p.Ser632=) n.2784C>T c.1113C>T (p.Ser371=) c.2307C>T (p.Ser769=) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91724178G>C | CA466339073 | ROR2 | c.2316C>G (p.Ser772=) c.1896C>G (p.Ser632=) n.2784C>G c.1113C>G (p.Ser371=) c.2307C>G (p.Ser769=) | |
| 9 | g.91724178G= | CA1863922250 | ROR2 | c.2316C= (p.Ser772=) c.1896C= (p.Ser632=) n.2784C= c.1113C= (p.Ser371=) c.2307C= (p.Ser769=) | |
| 9 | g.91724178G>T | CA466339071 | ROR2 | c.2316C>A (p.Ser772=) c.1896C>A (p.Ser632=) n.2784C>A c.1113C>A (p.Ser371=) c.2307C>A (p.Ser769=) | gnomAD v4 |
| 9 | g.91724179G>A | CA373794757 | ROR2 | c.2315C>T (p.Ser772Phe) c.1895C>T (p.Ser632Phe) n.2783C>T c.1112C>T (p.Ser371Phe) c.2306C>T (p.Ser769Phe) | COSMIC |
| 9 | g.91724179G>C | CA373794758 | ROR2 | c.2315C>G (p.Ser772Cys) c.1895C>G (p.Ser632Cys) n.2783C>G c.1112C>G (p.Ser371Cys) c.2306C>G (p.Ser769Cys) | |
| 9 | g.91724179G>T | CA373794759 | ROR2 | c.2315C>A (p.Ser772Tyr) c.1895C>A (p.Ser632Tyr) n.2783C>A c.1112C>A (p.Ser371Tyr) c.2306C>A (p.Ser769Tyr) | |
| 9 | g.91724180A= | CA1863922252 | ROR2 | c.2314T= (p.Ser772=) c.1894T= (p.Ser632=) n.2782T= c.1111T= (p.Ser371=) c.2305T= (p.Ser769=) | |
| 9 | g.91724180A>C | CA373794763 | ROR2 | c.2314T>G (p.Ser772Ala) c.1894T>G (p.Ser632Ala) n.2782T>G c.1111T>G (p.Ser371Ala) c.2305T>G (p.Ser769Ala) | |
| 9 | g.91724180A>G | CA373794765 | ROR2 | c.2314T>C (p.Ser772Pro) c.1894T>C (p.Ser632Pro) n.2782T>C c.1111T>C (p.Ser371Pro) c.2305T>C (p.Ser769Pro) | |
| 9 | g.91724180A>T | CA10634096 | ROR2 | c.2314T>A (p.Ser772Thr) c.1894T>A (p.Ser632Thr) n.2782T>A c.1111T>A (p.Ser371Thr) c.2305T>A (p.Ser769Thr) | ClinVar dbSNP |
| 9 | g.91724181G>A | CA466339075 | ROR2 | c.2313C>T (p.Ser771=) c.1893C>T (p.Ser631=) n.2781C>T c.1110C>T (p.Ser370=) c.2304C>T (p.Ser768=) | |
| 9 | g.91724181G>C | CA373794766 | ROR2 | c.2313C>G (p.Ser771Arg) c.1893C>G (p.Ser631Arg) n.2781C>G c.1110C>G (p.Ser370Arg) c.2304C>G (p.Ser768Arg) | |
| 9 | g.91724181G>T | CA373794767 | ROR2 | c.2313C>A (p.Ser771Arg) c.1893C>A (p.Ser631Arg) n.2781C>A c.1110C>A (p.Ser370Arg) c.2304C>A (p.Ser768Arg) | |
| 9 | g.91724182C>A | CA373794768 | ROR2 | c.2312G>T (p.Ser771Ile) c.1892G>T (p.Ser631Ile) n.2780G>T c.1109G>T (p.Ser370Ile) c.2303G>T (p.Ser768Ile) | |
| 9 | g.91724182C>G | CA373794769 | ROR2 | c.2312G>C (p.Ser771Thr) c.1892G>C (p.Ser631Thr) n.2780G>C c.1109G>C (p.Ser370Thr) c.2303G>C (p.Ser768Thr) | |
| 9 | g.91724182C>T | CA373794770 | ROR2 | c.2312G>A (p.Ser771Asn) c.1892G>A (p.Ser631Asn) n.2780G>A c.1109G>A (p.Ser370Asn) c.2303G>A (p.Ser768Asn) | |
| 9 | g.91724183T>A | CA373794772 | ROR2 | c.2311A>T (p.Ser771Cys) c.1891A>T (p.Ser631Cys) n.2779A>T c.1108A>T (p.Ser370Cys) c.2302A>T (p.Ser768Cys) | |
| 9 | g.91724183T>C | CA373794774 | ROR2 | c.2311A>G (p.Ser771Gly) c.1891A>G (p.Ser631Gly) n.2779A>G c.1108A>G (p.Ser370Gly) c.2302A>G (p.Ser768Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91724183T>G | CA373794776 | ROR2 | c.2311A>C (p.Ser771Arg) c.1891A>C (p.Ser631Arg) n.2779A>C c.1108A>C (p.Ser370Arg) c.2302A>C (p.Ser768Arg) | |
| 9 | g.91724183T= | CA1863922254 | ROR2 | c.2311A= (p.Ser771=) c.1891A= (p.Ser631=) n.2779A= c.1108A= (p.Ser370=) c.2302A= (p.Ser768=) | |
| 9 | g.91724184G>A | CA466339077 | ROR2 | c.2310C>T (p.Thr770=) c.1890C>T (p.Thr630=) n.2778C>T c.1107C>T (p.Thr369=) c.2301C>T (p.Thr767=) | |
| 9 | g.91724184G>C | CA466339079 | ROR2 | c.2310C>G (p.Thr770=) c.1890C>G (p.Thr630=) n.2778C>G c.1107C>G (p.Thr369=) c.2301C>G (p.Thr767=) | |
| 9 | g.91724184G>T | CA466339081 | ROR2 | c.2310C>A (p.Thr770=) c.1890C>A (p.Thr630=) n.2778C>A c.1107C>A (p.Thr369=) c.2301C>A (p.Thr767=) | gnomAD v4 |
| 9 | g.91724185G>A | CA373794777 | ROR2 | c.2309C>T (p.Thr770Ile) c.1889C>T (p.Thr630Ile) n.2777C>T c.1106C>T (p.Thr369Ile) c.2300C>T (p.Thr767Ile) | dbSNP gnomAD v4 |
| 9 | g.91724185G>C | CA373794781 | ROR2 | c.2309C>G (p.Thr770Ser) c.1889C>G (p.Thr630Ser) n.2777C>G c.1106C>G (p.Thr369Ser) c.2300C>G (p.Thr767Ser) | |
| 9 | g.91724185G= | CA1863922256 | ROR2 | c.2309C= (p.Thr770=) c.1889C= (p.Thr630=) n.2777C= c.1106C= (p.Thr369=) c.2300C= (p.Thr767=) | |
| 9 | g.91724185G>T | CA373794783 | ROR2 | c.2309C>A (p.Thr770Asn) c.1889C>A (p.Thr630Asn) n.2777C>A c.1106C>A (p.Thr369Asn) c.2300C>A (p.Thr767Asn) | gnomAD v4 |
| 9 | g.91724186T>A | CA373794785 | ROR2 | c.2308A>T (p.Thr770Ser) c.1888A>T (p.Thr630Ser) n.2776A>T c.1105A>T (p.Thr369Ser) c.2299A>T (p.Thr767Ser) | |
| 9 | g.91724186T>C | CA373794789 | ROR2 | c.2308A>G (p.Thr770Ala) c.1888A>G (p.Thr630Ala) n.2776A>G c.1105A>G (p.Thr369Ala) c.2299A>G (p.Thr767Ala) | |
| 9 | g.91724186T>G | CA373794791 | ROR2 | c.2308A>C (p.Thr770Pro) c.1888A>C (p.Thr630Pro) n.2776A>C c.1105A>C (p.Thr369Pro) c.2299A>C (p.Thr767Pro) | gnomAD v4 |
| 9 | g.91724187C>A | CA373794799 | ROR2 | c.2307G>T (p.Gln769His) c.1887G>T (p.Gln629His) n.2775G>T c.1104G>T (p.Gln368His) c.2298G>T (p.Gln766His) | |
| 9 | g.91724187C>G | CA373794798 | ROR2 | c.2307G>C (p.Gln769His) c.1887G>C (p.Gln629His) n.2775G>C c.1104G>C (p.Gln368His) c.2298G>C (p.Gln766His) | |
| 9 | g.91724187C>T | CA466339083 | ROR2 | c.2307G>A (p.Gln769=) c.1887G>A (p.Gln629=) n.2775G>A c.1104G>A (p.Gln368=) c.2298G>A (p.Gln766=) | |
| 9 | g.91724188T>A | CA373794802 | ROR2 | c.2306A>T (p.Gln769Leu) c.1886A>T (p.Gln629Leu) n.2774A>T c.1103A>T (p.Gln368Leu) c.2297A>T (p.Gln766Leu) | gnomAD v4 |
| 9 | g.91724188T>C | CA373794805 | ROR2 | c.2306A>G (p.Gln769Arg) c.1886A>G (p.Gln629Arg) n.2774A>G c.1103A>G (p.Gln368Arg) c.2297A>G (p.Gln766Arg) | |
| 9 | g.91724188T>G | CA373794808 | ROR2 | c.2306A>C (p.Gln769Pro) c.1886A>C (p.Gln629Pro) n.2774A>C c.1103A>C (p.Gln368Pro) c.2297A>C (p.Gln766Pro) | |
| 9 | g.91724189G>A | CA373794809 | ROR2 | c.2305C>T (p.Gln769Ter) c.1885C>T (p.Gln629Ter) n.2773C>T c.1102C>T (p.Gln368Ter) c.2296C>T (p.Gln766Ter) | ClinVar dbSNP |
| 9 | g.91724189G>C | CA373794810 | ROR2 | c.2305C>G (p.Gln769Glu) c.1885C>G (p.Gln629Glu) n.2773C>G c.1102C>G (p.Gln368Glu) c.2296C>G (p.Gln766Glu) | |
| 9 | g.91724189G= | CA1863922257 | ROR2 | c.2305C= (p.Gln769=) c.1885C= (p.Gln629=) n.2773C= c.1102C= (p.Gln368=) c.2296C= (p.Gln766=) | |
| 9 | g.91724189G>T | CA373794811 | ROR2 | c.2305C>A (p.Gln769Lys) c.1885C>A (p.Gln629Lys) n.2773C>A c.1102C>A (p.Gln368Lys) c.2296C>A (p.Gln766Lys) | |
| 9 | g.91724190C>A | CA466339084 | ROR2 | c.2304G>T (p.Thr768=) c.1884G>T (p.Thr628=) n.2772G>T c.1101G>T (p.Thr367=) c.2295G>T (p.Thr765=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724190C= | CA1863922259 | ROR2 | c.2304G= (p.Thr768=) c.1884G= (p.Thr628=) n.2772G= c.1101G= (p.Thr367=) c.2295G= (p.Thr765=) | |
| 9 | g.91724190C>G | CA466339086 | ROR2 | c.2304G>C (p.Thr768=) c.1884G>C (p.Thr628=) n.2772G>C c.1101G>C (p.Thr367=) c.2295G>C (p.Thr765=) | |
| 9 | g.91724190C>T | CA5120422 | ROR2 | c.2304G>A (p.Thr768=) c.1884G>A (p.Thr628=) n.2772G>A c.1101G>A (p.Thr367=) c.2295G>A (p.Thr765=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724191G>A | CA5120423 | ROR2 | c.2303C>T (p.Thr768Met) c.1883C>T (p.Thr628Met) n.2771C>T c.1100C>T (p.Thr367Met) c.2294C>T (p.Thr765Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724191G>C | CA373794812 | ROR2 | c.2303C>G (p.Thr768Arg) c.1883C>G (p.Thr628Arg) n.2771C>G c.1100C>G (p.Thr367Arg) c.2294C>G (p.Thr765Arg) | |
| 9 | g.91724191G= | CA1863922261 | ROR2 | c.2303C= (p.Thr768=) c.1883C= (p.Thr628=) n.2771C= c.1100C= (p.Thr367=) c.2294C= (p.Thr765=) | |
| 9 | g.91724191G>T | CA373794815 | ROR2 | c.2303C>A (p.Thr768Lys) c.1883C>A (p.Thr628Lys) n.2771C>A c.1100C>A (p.Thr367Lys) c.2294C>A (p.Thr765Lys) | gnomAD v4 |
| 9 | g.91724192T>A | CA373794818 | ROR2 | c.2302A>T (p.Thr768Ser) c.1882A>T (p.Thr628Ser) n.2770A>T c.1099A>T (p.Thr367Ser) c.2293A>T (p.Thr765Ser) | |
| 9 | g.91724192T>C | CA373794819 | ROR2 | c.2302A>G (p.Thr768Ala) c.1882A>G (p.Thr628Ala) n.2770A>G c.1099A>G (p.Thr367Ala) c.2293A>G (p.Thr765Ala) | |
| 9 | g.91724192T>G | CA373794821 | ROR2 | c.2302A>C (p.Thr768Pro) c.1882A>C (p.Thr628Pro) n.2770A>C c.1099A>C (p.Thr367Pro) c.2293A>C (p.Thr765Pro) | |
| 9 | g.91724193G>A | CA5120424 | ROR2 | c.2301C>T (p.Thr767=) c.1881C>T (p.Thr627=) n.2769C>T c.1098C>T (p.Thr366=) c.2292C>T (p.Thr764=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724193G>C | CA466339090 | ROR2 | c.2301C>G (p.Thr767=) c.1881C>G (p.Thr627=) n.2769C>G c.1098C>G (p.Thr366=) c.2292C>G (p.Thr764=) | |
| 9 | g.91724193G= | CA1863922264 | ROR2 | c.2301C= (p.Thr767=) c.1881C= (p.Thr627=) n.2769C= c.1098C= (p.Thr366=) c.2292C= (p.Thr764=) | |
| 9 | g.91724193G>T | CA466339091 | ROR2 | c.2301C>A (p.Thr767=) c.1881C>A (p.Thr627=) n.2769C>A c.1098C>A (p.Thr366=) c.2292C>A (p.Thr764=) | |
| 9 | g.91724194G>A | CA373794832 | ROR2 | c.2300C>T (p.Thr767Ile) c.1880C>T (p.Thr627Ile) n.2768C>T c.1097C>T (p.Thr366Ile) c.2291C>T (p.Thr764Ile) | gnomAD v4 |
| 9 | g.91724194G>C | CA373794826 | ROR2 | c.2300C>G (p.Thr767Ser) c.1880C>G (p.Thr627Ser) n.2768C>G c.1097C>G (p.Thr366Ser) c.2291C>G (p.Thr764Ser) | |
| 9 | g.91724194G= | CA1863922322 | ROR2 | c.2300C= (p.Thr767=) c.1880C= (p.Thr627=) n.2768C= c.1097C= (p.Thr366=) c.2291C= (p.Thr764=) | |
| 9 | g.91724194G>T | CA5120425 | ROR2 | c.2300C>A (p.Thr767Asn) c.1880C>A (p.Thr627Asn) n.2768C>A c.1097C>A (p.Thr366Asn) c.2291C>A (p.Thr764Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724195T>A | CA373794833 | ROR2 | c.2299A>T (p.Thr767Ser) c.1879A>T (p.Thr627Ser) n.2767A>T c.1096A>T (p.Thr366Ser) c.2290A>T (p.Thr764Ser) | |
| 9 | g.91724195T>C | CA373794834 | ROR2 | c.2299A>G (p.Thr767Ala) c.1879A>G (p.Thr627Ala) n.2767A>G c.1096A>G (p.Thr366Ala) c.2290A>G (p.Thr764Ala) | |
| 9 | g.91724195T>G | CA373794839 | ROR2 | c.2299A>C (p.Thr767Pro) c.1879A>C (p.Thr627Pro) n.2767A>C c.1096A>C (p.Thr366Pro) c.2290A>C (p.Thr764Pro) | |
| 9 | g.91724196G>A | CA466339093 | ROR2 | c.2298C>T (p.Asn766=) c.1878C>T (p.Asn626=) n.2766C>T c.1095C>T (p.Asn365=) c.2289C>T (p.Asn763=) | |
| 9 | g.91724196G>C | CA373794843 | ROR2 | c.2298C>G (p.Asn766Lys) c.1878C>G (p.Asn626Lys) n.2766C>G c.1095C>G (p.Asn365Lys) c.2289C>G (p.Asn763Lys) | |
| 9 | g.91724196G>T | CA373794845 | ROR2 | c.2298C>A (p.Asn766Lys) c.1878C>A (p.Asn626Lys) n.2766C>A c.1095C>A (p.Asn365Lys) c.2289C>A (p.Asn763Lys) | gnomAD v4 |
| 9 | g.91724197T>A | CA373794847 | ROR2 | c.2297A>T (p.Asn766Ile) c.1877A>T (p.Asn626Ile) n.2765A>T c.1094A>T (p.Asn365Ile) c.2288A>T (p.Asn763Ile) | |
| 9 | g.91724197T>C | CA373794849 | ROR2 | c.2297A>G (p.Asn766Ser) c.1877A>G (p.Asn626Ser) n.2765A>G c.1094A>G (p.Asn365Ser) c.2288A>G (p.Asn763Ser) | gnomAD v4 |
| 9 | g.91724197T>G | CA373794851 | ROR2 | c.2297A>C (p.Asn766Thr) c.1877A>C (p.Asn626Thr) n.2765A>C c.1094A>C (p.Asn365Thr) c.2288A>C (p.Asn763Thr) | |
| 9 | g.91724198T>A | CA373794853 | ROR2 | c.2296A>T (p.Asn766Tyr) c.1876A>T (p.Asn626Tyr) n.2764A>T c.1093A>T (p.Asn365Tyr) c.2287A>T (p.Asn763Tyr) | |
| 9 | g.91724198T>C | CA373794855 | ROR2 | c.2296A>G (p.Asn766Asp) c.1876A>G (p.Asn626Asp) n.2764A>G c.1093A>G (p.Asn365Asp) c.2287A>G (p.Asn763Asp) | |
| 9 | g.91724198T>G | CA373794856 | ROR2 | c.2296A>C (p.Asn766His) c.1876A>C (p.Asn626His) n.2764A>C c.1093A>C (p.Asn365His) c.2287A>C (p.Asn763His) | |
| 9 | g.91724199G>A | CA5120426 | ROR2 | c.2295C>T (p.Ser765=) c.1875C>T (p.Ser625=) n.2763C>T c.1092C>T (p.Ser364=) c.2286C>T (p.Ser762=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724199G>C | CA373794857 | ROR2 | c.2295C>G (p.Ser765Arg) c.1875C>G (p.Ser625Arg) n.2763C>G c.1092C>G (p.Ser364Arg) c.2286C>G (p.Ser762Arg) | |
| 9 | g.91724199G= | CA1863922326 | ROR2 | c.2295C= (p.Ser765=) c.1875C= (p.Ser625=) n.2763C= c.1092C= (p.Ser364=) c.2286C= (p.Ser762=) | |
| 9 | g.91724199G>T | CA373794858 | ROR2 | c.2295C>A (p.Ser765Arg) c.1875C>A (p.Ser625Arg) n.2763C>A c.1092C>A (p.Ser364Arg) c.2286C>A (p.Ser762Arg) | |
| 9 | g.91724200C>A | CA373794860 | ROR2 | c.2294G>T (p.Ser765Ile) c.1874G>T (p.Ser625Ile) n.2762G>T c.1091G>T (p.Ser364Ile) c.2285G>T (p.Ser762Ile) | |
| 9 | g.91724200C>G | CA373794862 | ROR2 | c.2294G>C (p.Ser765Thr) c.1874G>C (p.Ser625Thr) n.2762G>C c.1091G>C (p.Ser364Thr) c.2285G>C (p.Ser762Thr) | |
| 9 | g.91724200C>T | CA373794864 | ROR2 | c.2294G>A (p.Ser765Asn) c.1874G>A (p.Ser625Asn) n.2762G>A c.1091G>A (p.Ser364Asn) c.2285G>A (p.Ser762Asn) | |
| 9 | g.91724201T>A | CA373794867 | ROR2 | c.2293A>T (p.Ser765Cys) c.1873A>T (p.Ser625Cys) n.2761A>T c.1090A>T (p.Ser364Cys) c.2284A>T (p.Ser762Cys) | |
| 9 | g.91724201T>C | CA373794868 | ROR2 | c.2293A>G (p.Ser765Gly) c.1873A>G (p.Ser625Gly) n.2761A>G c.1090A>G (p.Ser364Gly) c.2284A>G (p.Ser762Gly) | gnomAD v4 |
| 9 | g.91724201T>G | CA373794869 | ROR2 | c.2293A>C (p.Ser765Arg) c.1873A>C (p.Ser625Arg) n.2761A>C c.1090A>C (p.Ser364Arg) c.2284A>C (p.Ser762Arg) | |
| 9 | g.91724202G>A | CA466339100 | ROR2 | c.2292C>T (p.Ala764=) c.1872C>T (p.Ala624=) n.2760C>T c.1089C>T (p.Ala363=) c.2283C>T (p.Ala761=) | |
| 9 | g.91724202G>C | CA466339098 | ROR2 | c.2292C>G (p.Ala764=) c.1872C>G (p.Ala624=) n.2760C>G c.1089C>G (p.Ala363=) c.2283C>G (p.Ala761=) | |
| 9 | g.91724202G>T | CA466339097 | ROR2 | c.2292C>A (p.Ala764=) c.1872C>A (p.Ala624=) n.2760C>A c.1089C>A (p.Ala363=) c.2283C>A (p.Ala761=) | gnomAD v4 |
| 9 | g.91724203G>A | CA373794870 | ROR2 | c.2291C>T (p.Ala764Val) c.1871C>T (p.Ala624Val) n.2759C>T c.1088C>T (p.Ala363Val) c.2282C>T (p.Ala761Val) | gnomAD v4 |
| 9 | g.91724203G>C | CA373794871 | ROR2 | c.2291C>G (p.Ala764Gly) c.1871C>G (p.Ala624Gly) n.2759C>G c.1088C>G (p.Ala363Gly) c.2282C>G (p.Ala761Gly) | |
| 9 | g.91724203G>T | CA373794875 | ROR2 | c.2291C>A (p.Ala764Asp) c.1871C>A (p.Ala624Asp) n.2759C>A c.1088C>A (p.Ala363Asp) c.2282C>A (p.Ala761Asp) | gnomAD v4 |
| 9 | g.91724204C>A | CA373794876 | ROR2 | c.2290G>T (p.Ala764Ser) c.1870G>T (p.Ala624Ser) n.2758G>T c.1087G>T (p.Ala363Ser) c.2281G>T (p.Ala761Ser) | |
| 9 | g.91724204C= | CA1863922331 | ROR2 | c.2290G= (p.Ala764=) c.1870G= (p.Ala624=) n.2758G= c.1087G= (p.Ala363=) c.2281G= (p.Ala761=) | |
| 9 | g.91724204C>G | CA373794882 | ROR2 | c.2290G>C (p.Ala764Pro) c.1870G>C (p.Ala624Pro) n.2758G>C c.1087G>C (p.Ala363Pro) c.2281G>C (p.Ala761Pro) | |
| 9 | g.91724204C>T | CA5120427 | ROR2 | c.2290G>A (p.Ala764Thr) c.1870G>A (p.Ala624Thr) n.2758G>A c.1087G>A (p.Ala363Thr) c.2281G>A (p.Ala761Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724208del | CA645560445 | ROR2 | c.2290del (p.Ala764ProfsTer10) c.1870del (p.Ala624ProfsTer10) n.2758del c.1087del (p.Ala363ProfsTer10) c.2281del (p.Ala761ProfsTer10) | ClinVar gnomAD v4 COSMIC |
| 9 | g.91724205C>A | CA466339101 | ROR2 | c.2289G>T (p.Gly763=) c.1869G>T (p.Gly623=) n.2757G>T c.1086G>T (p.Gly362=) c.2280G>T (p.Gly760=) | |
| 9 | g.91724205C= | CA1863922334 | ROR2 | c.2289G= (p.Gly763=) c.1869G= (p.Gly623=) n.2757G= c.1086G= (p.Gly362=) c.2280G= (p.Gly760=) | |
| 9 | g.91724205C>G | CA466339103 | ROR2 | c.2289G>C (p.Gly763=) c.1869G>C (p.Gly623=) n.2757G>C c.1086G>C (p.Gly362=) c.2280G>C (p.Gly760=) | gnomAD v4 |
| 9 | g.91724205C>T | CA466339102 | ROR2 | c.2289G>A (p.Gly763=) c.1869G>A (p.Gly623=) n.2757G>A c.1086G>A (p.Gly362=) c.2280G>A (p.Gly760=) | dbSNP gnomAD v2 |
| 9 | g.91724206C>A | CA373794889 | ROR2 | c.2288G>T (p.Gly763Val) c.1868G>T (p.Gly623Val) n.2756G>T c.1085G>T (p.Gly362Val) c.2279G>T (p.Gly760Val) | |
| 9 | g.91724206C>G | CA373794891 | ROR2 | c.2288G>C (p.Gly763Ala) c.1868G>C (p.Gly623Ala) n.2756G>C c.1085G>C (p.Gly362Ala) c.2279G>C (p.Gly760Ala) | |
| 9 | g.91724206C>T | CA373794884 | ROR2 | c.2288G>A (p.Gly763Glu) c.1868G>A (p.Gly623Glu) n.2756G>A c.1085G>A (p.Gly362Glu) c.2279G>A (p.Gly760Glu) | |
| 9 | g.91724207C>A | CA373794896 | ROR2 | c.2287G>T (p.Gly763Trp) c.1867G>T (p.Gly623Trp) n.2755G>T c.1084G>T (p.Gly362Trp) c.2278G>T (p.Gly760Trp) | |
| 9 | g.91724207C>G | CA373794899 | ROR2 | c.2287G>C (p.Gly763Arg) c.1867G>C (p.Gly623Arg) n.2755G>C c.1084G>C (p.Gly362Arg) c.2278G>C (p.Gly760Arg) | |
| 9 | g.91724207C>T | CA373794898 | ROR2 | c.2287G>A (p.Gly763Arg) c.1867G>A (p.Gly623Arg) n.2755G>A c.1084G>A (p.Gly362Arg) c.2278G>A (p.Gly760Arg) | |
| 9 | g.91724208C>A | CA466339104 | ROR2 | c.2286G>T (p.Ser762=) c.1866G>T (p.Ser622=) n.2754G>T c.1083G>T (p.Ser361=) c.2277G>T (p.Ser759=) | |
| 9 | g.91724208C= | CA1863922341 | ROR2 | c.2286G= (p.Ser762=) c.1866G= (p.Ser622=) n.2754G= c.1083G= (p.Ser361=) c.2277G= (p.Ser759=) | |
| 9 | g.91724208C>G | CA466339105 | ROR2 | c.2286G>C (p.Ser762=) c.1866G>C (p.Ser622=) n.2754G>C c.1083G>C (p.Ser361=) c.2277G>C (p.Ser759=) | |
| 9 | g.91724208C>T | CA5120428 | ROR2 | c.2286G>A (p.Ser762=) c.1866G>A (p.Ser622=) n.2754G>A c.1083G>A (p.Ser361=) c.2277G>A (p.Ser759=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724209G>A | CA173326 | ROR2 | c.2285C>T (p.Ser762Leu) c.1865C>T (p.Ser622Leu) n.2753C>T c.1082C>T (p.Ser361Leu) c.2276C>T (p.Ser759Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724209G>C | CA373794908 | ROR2 | c.2285C>G (p.Ser762Trp) c.1865C>G (p.Ser622Trp) n.2753C>G c.1082C>G (p.Ser361Trp) c.2276C>G (p.Ser759Trp) | |
| 9 | g.91724209G= | CA1863922344 | ROR2 | c.2285C= (p.Ser762=) c.1865C= (p.Ser622=) n.2753C= c.1082C= (p.Ser361=) c.2276C= (p.Ser759=) | |
| 9 | g.91724209G>T | CA373794912 | ROR2 | c.2285C>A (p.Ser762Ter) c.1865C>A (p.Ser622Ter) n.2753C>A c.1082C>A (p.Ser361Ter) c.2276C>A (p.Ser759Ter) | gnomAD v4 |
| 9 | g.91724210A>C | CA373794914 | ROR2 | c.2284T>G (p.Ser762Ala) c.1864T>G (p.Ser622Ala) n.2752T>G c.1081T>G (p.Ser361Ala) c.2275T>G (p.Ser759Ala) | gnomAD v4 |
| 9 | g.91724210A>G | CA373794917 | ROR2 | c.2284T>C (p.Ser762Pro) c.1864T>C (p.Ser622Pro) n.2752T>C c.1081T>C (p.Ser361Pro) c.2275T>C (p.Ser759Pro) | |
| 9 | g.91724210A>T | CA373794916 | ROR2 | c.2284T>A (p.Ser762Thr) c.1864T>A (p.Ser622Thr) n.2752T>A c.1081T>A (p.Ser361Thr) c.2275T>A (p.Ser759Thr) | |
| 9 | g.91724211G>A | CA5120429 | ROR2 | c.2283C>T (p.Thr761=) c.1863C>T (p.Thr621=) n.2751C>T c.1080C>T (p.Thr360=) c.2274C>T (p.Thr758=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724211G>C | CA466339107 | ROR2 | c.2283C>G (p.Thr761=) c.1863C>G (p.Thr621=) n.2751C>G c.1080C>G (p.Thr360=) c.2274C>G (p.Thr758=) | gnomAD v4 |
| 9 | g.91724211G= | CA1863922349 | ROR2 | c.2283C= (p.Thr761=) c.1863C= (p.Thr621=) n.2751C= c.1080C= (p.Thr360=) c.2274C= (p.Thr758=) | |
| 9 | g.91724211G>T | CA466339109 | ROR2 | c.2283C>A (p.Thr761=) c.1863C>A (p.Thr621=) n.2751C>A c.1080C>A (p.Thr360=) c.2274C>A (p.Thr758=) | |
| 9 | g.91724212G>A | CA373794921 | ROR2 | c.2282C>T (p.Thr761Ile) c.1862C>T (p.Thr621Ile) n.2750C>T c.1079C>T (p.Thr360Ile) c.2273C>T (p.Thr758Ile) | dbSNP gnomAD v4 |
| 9 | g.91724212G>C | CA373794919 | ROR2 | c.2282C>G (p.Thr761Ser) c.1862C>G (p.Thr621Ser) n.2750C>G c.1079C>G (p.Thr360Ser) c.2273C>G (p.Thr758Ser) | |
| 9 | g.91724212G= | CA1863922351 | ROR2 | c.2282C= (p.Thr761=) c.1862C= (p.Thr621=) n.2750C= c.1079C= (p.Thr360=) c.2273C= (p.Thr758=) | |
| 9 | g.91724212G>T | CA373794920 | ROR2 | c.2282C>A (p.Thr761Asn) c.1862C>A (p.Thr621Asn) n.2750C>A c.1079C>A (p.Thr360Asn) c.2273C>A (p.Thr758Asn) | |
| 9 | g.91724213T>A | CA373794923 | ROR2 | c.2281A>T (p.Thr761Ser) c.1861A>T (p.Thr621Ser) n.2749A>T c.1078A>T (p.Thr360Ser) c.2272A>T (p.Thr758Ser) | |
| 9 | g.91724213T>C | CA373794924 | ROR2 | c.2281A>G (p.Thr761Ala) c.1861A>G (p.Thr621Ala) n.2749A>G c.1078A>G (p.Thr360Ala) c.2272A>G (p.Thr758Ala) | |
| 9 | g.91724213T>G | CA373794926 | ROR2 | c.2281A>C (p.Thr761Pro) c.1861A>C (p.Thr621Pro) n.2749A>C c.1078A>C (p.Thr360Pro) c.2272A>C (p.Thr758Pro) | dbSNP |
| 9 | g.91724213T= | CA1863922353 | ROR2 | c.2281A= (p.Thr761=) c.1861A= (p.Thr621=) n.2749A= c.1078A= (p.Thr360=) c.2272A= (p.Thr758=) | |
| 9 | g.91724214C>A | CA373794928 | ROR2 | c.2280G>T (p.Gln760His) c.1860G>T (p.Gln620His) n.2748G>T c.1077G>T (p.Gln359His) c.2271G>T (p.Gln757His) | |
| 9 | g.91724214C>G | CA373794930 | ROR2 | c.2280G>C (p.Gln760His) c.1860G>C (p.Gln620His) n.2748G>C c.1077G>C (p.Gln359His) c.2271G>C (p.Gln757His) | |
| 9 | g.91724214C>T | CA466339113 | ROR2 | c.2280G>A (p.Gln760=) c.1860G>A (p.Gln620=) n.2748G>A c.1077G>A (p.Gln359=) c.2271G>A (p.Gln757=) | |
| 9 | g.91724215T>A | CA373794932 | ROR2 | c.2279A>T (p.Gln760Leu) c.1859A>T (p.Gln620Leu) n.2747A>T c.1076A>T (p.Gln359Leu) c.2270A>T (p.Gln757Leu) | dbSNP |
| 9 | g.91724215T>C | CA373794936 | ROR2 | c.2279A>G (p.Gln760Arg) c.1859A>G (p.Gln620Arg) n.2747A>G c.1076A>G (p.Gln359Arg) c.2270A>G (p.Gln757Arg) | |
| 9 | g.91724215T>G | CA373794934 | ROR2 | c.2279A>C (p.Gln760Pro) c.1859A>C (p.Gln620Pro) n.2747A>C c.1076A>C (p.Gln359Pro) c.2270A>C (p.Gln757Pro) | dbSNP |
| 9 | g.91724215T= | CA1863922356 | ROR2 | c.2279A= (p.Gln760=) c.1859A= (p.Gln620=) n.2747A= c.1076A= (p.Gln359=) c.2270A= (p.Gln757=) | |
| 9 | g.91724216G>A | CA373794942 | ROR2 | c.2278C>T (p.Gln760Ter) c.1858C>T (p.Gln620Ter) n.2746C>T c.1075C>T (p.Gln359Ter) c.2269C>T (p.Gln757Ter) | ClinVar |
| 9 | g.91724216G>C | CA373794944 | ROR2 | c.2278C>G (p.Gln760Glu) c.1858C>G (p.Gln620Glu) n.2746C>G c.1075C>G (p.Gln359Glu) c.2269C>G (p.Gln757Glu) | |
| 9 | g.91724216G>T | CA373794949 | ROR2 | c.2278C>A (p.Gln760Lys) c.1858C>A (p.Gln620Lys) n.2746C>A c.1075C>A (p.Gln359Lys) c.2269C>A (p.Gln757Lys) | gnomAD v4 |
| 9 | g.91724217C>A | CA466339114 | ROR2 | c.2277G>T (p.Ala759=) c.1857G>T (p.Ala619=) n.2745G>T c.1074G>T (p.Ala358=) c.2268G>T (p.Ala756=) | |
| 9 | g.91724217C= | CA1863922362 | ROR2 | c.2277G= (p.Ala759=) c.1857G= (p.Ala619=) n.2745G= c.1074G= (p.Ala358=) c.2268G= (p.Ala756=) | |
| 9 | g.91724217C>G | CA466339115 | ROR2 | c.2277G>C (p.Ala759=) c.1857G>C (p.Ala619=) n.2745G>C c.1074G>C (p.Ala358=) c.2268G>C (p.Ala756=) | |
| 9 | g.91724217C>T | CA5120430 | ROR2 | c.2277G>A (p.Ala759=) c.1857G>A (p.Ala619=) n.2745G>A c.1074G>A (p.Ala358=) c.2268G>A (p.Ala756=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724218G>A | CA373794954 | ROR2 | c.2276C>T (p.Ala759Val) c.1856C>T (p.Ala619Val) n.2744C>T c.1073C>T (p.Ala358Val) c.2267C>T (p.Ala756Val) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724218G>C | CA373794959 | ROR2 | c.2276C>G (p.Ala759Gly) c.1856C>G (p.Ala619Gly) n.2744C>G c.1073C>G (p.Ala358Gly) c.2267C>G (p.Ala756Gly) | |
| 9 | g.91724218G= | CA1863922368 | ROR2 | c.2276C= (p.Ala759=) c.1856C= (p.Ala619=) n.2744C= c.1073C= (p.Ala358=) c.2267C= (p.Ala756=) | |
| 9 | g.91724218G>T | CA373794956 | ROR2 | c.2276C>A (p.Ala759Glu) c.1856C>A (p.Ala619Glu) n.2744C>A c.1073C>A (p.Ala358Glu) c.2267C>A (p.Ala756Glu) | |
| 9 | g.91724219C>A | CA373794960 | ROR2 | c.2275G>T (p.Ala759Ser) c.1855G>T (p.Ala619Ser) n.2743G>T c.1072G>T (p.Ala358Ser) c.2266G>T (p.Ala756Ser) | |
| 9 | g.91724219C>G | CA373794961 | ROR2 | c.2275G>C (p.Ala759Pro) c.1855G>C (p.Ala619Pro) n.2743G>C c.1072G>C (p.Ala358Pro) c.2266G>C (p.Ala756Pro) | |
| 9 | g.91724219C>T | CA373794962 | ROR2 | c.2275G>A (p.Ala759Thr) c.1855G>A (p.Ala619Thr) n.2743G>A c.1072G>A (p.Ala358Thr) c.2266G>A (p.Ala756Thr) | |
| 9 | g.91724220C>A | CA5120431 | ROR2 | c.2274G>T (p.Ser758=) c.1854G>T (p.Ser618=) n.2742G>T c.1071G>T (p.Ser357=) c.2265G>T (p.Ser755=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724220C= | CA1863922376 | ROR2 | c.2274G= (p.Ser758=) c.1854G= (p.Ser618=) n.2742G= c.1071G= (p.Ser357=) c.2265G= (p.Ser755=) | |
| 9 | g.91724220C>G | CA466339120 | ROR2 | c.2274G>C (p.Ser758=) c.1854G>C (p.Ser618=) n.2742G>C c.1071G>C (p.Ser357=) c.2265G>C (p.Ser755=) | |
| 9 | g.91724220C>T | CA5120432 | ROR2 | c.2274G>A (p.Ser758=) c.1854G>A (p.Ser618=) n.2742G>A c.1071G>A (p.Ser357=) c.2265G>A (p.Ser755=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724221G>A | CA5120433 | ROR2 | c.2273C>T (p.Ser758Leu) c.1853C>T (p.Ser618Leu) n.2741C>T c.1070C>T (p.Ser357Leu) c.2264C>T (p.Ser755Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724221G>C | CA373794965 | ROR2 | c.2273C>G (p.Ser758Trp) c.1853C>G (p.Ser618Trp) n.2741C>G c.1070C>G (p.Ser357Trp) c.2264C>G (p.Ser755Trp) | |
| 9 | g.91724221G= | CA1863922378 | ROR2 | c.2273C= (p.Ser758=) c.1853C= (p.Ser618=) n.2741C= c.1070C= (p.Ser357=) c.2264C= (p.Ser755=) | |
| 9 | g.91724221G>T | CA373794966 | ROR2 | c.2273C>A (p.Ser758Ter) c.1853C>A (p.Ser618Ter) n.2741C>A c.1070C>A (p.Ser357Ter) c.2264C>A (p.Ser755Ter) | |
| 9 | g.91724222A= | CA1863922381 | ROR2 | c.2272T= (p.Ser758=) c.1852T= (p.Ser618=) n.2740T= c.1069T= (p.Ser357=) c.2263T= (p.Ser755=) | |
| 9 | g.91724222A>C | CA373794967 | ROR2 | c.2272T>G (p.Ser758Ala) c.1852T>G (p.Ser618Ala) n.2740T>G c.1069T>G (p.Ser357Ala) c.2263T>G (p.Ser755Ala) | |
| 9 | g.91724222A>G | CA373794968 | ROR2 | c.2272T>C (p.Ser758Pro) c.1852T>C (p.Ser618Pro) n.2740T>C c.1069T>C (p.Ser357Pro) c.2263T>C (p.Ser755Pro) | dbSNP |
| 9 | g.91724222A>T | CA373794971 | ROR2 | c.2272T>A (p.Ser758Thr) c.1852T>A (p.Ser618Thr) n.2740T>A c.1069T>A (p.Ser357Thr) c.2263T>A (p.Ser755Thr) | |
| 9 | g.91724223G>A | CA466339124 | ROR2 | c.2271C>T (p.Ser757=) c.1851C>T (p.Ser617=) n.2739C>T c.1068C>T (p.Ser356=) c.2262C>T (p.Ser754=) | |
| 9 | g.91724223G>C | CA373794975 | ROR2 | c.2271C>G (p.Ser757Arg) c.1851C>G (p.Ser617Arg) n.2739C>G c.1068C>G (p.Ser356Arg) c.2262C>G (p.Ser754Arg) | |
| 9 | g.91724223G>T | CA373794977 | ROR2 | c.2271C>A (p.Ser757Arg) c.1851C>A (p.Ser617Arg) n.2739C>A c.1068C>A (p.Ser356Arg) c.2262C>A (p.Ser754Arg) | |
| 9 | g.91724224C>A | CA373794980 | ROR2 | c.2270G>T (p.Ser757Ile) c.1850G>T (p.Ser617Ile) n.2738G>T c.1067G>T (p.Ser356Ile) c.2261G>T (p.Ser754Ile) | |
| 9 | g.91724224C>G | CA373794981 | ROR2 | c.2270G>C (p.Ser757Thr) c.1850G>C (p.Ser617Thr) n.2738G>C c.1067G>C (p.Ser356Thr) c.2261G>C (p.Ser754Thr) | |
| 9 | g.91724224C>T | CA373794984 | ROR2 | c.2270G>A (p.Ser757Asn) c.1850G>A (p.Ser617Asn) n.2738G>A c.1067G>A (p.Ser356Asn) c.2261G>A (p.Ser754Asn) | dbSNP |
| 9 | g.91724225T>A | CA373794986 | ROR2 | c.2269A>T (p.Ser757Cys) c.1849A>T (p.Ser617Cys) n.2737A>T c.1066A>T (p.Ser356Cys) c.2260A>T (p.Ser754Cys) | |
| 9 | g.91724225T>C | CA5120434 | ROR2 | c.2269A>G (p.Ser757Gly) c.1849A>G (p.Ser617Gly) n.2737A>G c.1066A>G (p.Ser356Gly) c.2260A>G (p.Ser754Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724225T>G | CA373794991 | ROR2 | c.2269A>C (p.Ser757Arg) c.1849A>C (p.Ser617Arg) n.2737A>C c.1066A>C (p.Ser356Arg) c.2260A>C (p.Ser754Arg) | |
| 9 | g.91724225T= | CA1863922386 | ROR2 | c.2269A= (p.Ser757=) c.1849A= (p.Ser617=) n.2737A= c.1066A= (p.Ser356=) c.2260A= (p.Ser754=) | |
| 9 | g.91724226G>A | CA466339125 | ROR2 | c.2268C>T (p.Asn756=) c.1848C>T (p.Asn616=) n.2736C>T c.1065C>T (p.Asn355=) c.2259C>T (p.Asn753=) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91724226G>C | CA373794996 | ROR2 | c.2268C>G (p.Asn756Lys) c.1848C>G (p.Asn616Lys) n.2736C>G c.1065C>G (p.Asn355Lys) c.2259C>G (p.Asn753Lys) | |
| 9 | g.91724226G= | CA1863922389 | ROR2 | c.2268C= (p.Asn756=) c.1848C= (p.Asn616=) n.2736C= c.1065C= (p.Asn355=) c.2259C= (p.Asn753=) | |
| 9 | g.91724226G>T | CA373794993 | ROR2 | c.2268C>A (p.Asn756Lys) c.1848C>A (p.Asn616Lys) n.2736C>A c.1065C>A (p.Asn355Lys) c.2259C>A (p.Asn753Lys) | |
| 9 | g.91724227T>A | CA373795002 | ROR2 | c.2267A>T (p.Asn756Ile) c.1847A>T (p.Asn616Ile) n.2735A>T c.1064A>T (p.Asn355Ile) c.2258A>T (p.Asn753Ile) | |
| 9 | g.91724227T>C | CA373795004 | ROR2 | c.2267A>G (p.Asn756Ser) c.1847A>G (p.Asn616Ser) n.2735A>G c.1064A>G (p.Asn355Ser) c.2258A>G (p.Asn753Ser) | ClinVar dbSNP gnomAD v4 |
| 9 | g.91724227T>G | CA373795009 | ROR2 | c.2267A>C (p.Asn756Thr) c.1847A>C (p.Asn616Thr) n.2735A>C c.1064A>C (p.Asn355Thr) c.2258A>C (p.Asn753Thr) | |
| 9 | g.91724228T>A | CA373795013 | ROR2 | c.2266A>T (p.Asn756Tyr) c.1846A>T (p.Asn616Tyr) n.2734A>T c.1063A>T (p.Asn355Tyr) c.2257A>T (p.Asn753Tyr) | |
| 9 | g.91724228T>C | CA5120435 | ROR2 | c.2266A>G (p.Asn756Asp) c.1846A>G (p.Asn616Asp) n.2734A>G c.1063A>G (p.Asn355Asp) c.2257A>G (p.Asn753Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724228T>G | CA373795018 | ROR2 | c.2266A>C (p.Asn756His) c.1846A>C (p.Asn616His) n.2734A>C c.1063A>C (p.Asn355His) c.2257A>C (p.Asn753His) | |
| 9 | g.91724228T= | CA1863922391 | ROR2 | c.2266A= (p.Asn756=) c.1846A= (p.Asn616=) n.2734A= c.1063A= (p.Asn355=) c.2257A= (p.Asn753=) | |
| 9 | g.91724229G>A | CA5120436 | ROR2 | c.2265C>T (p.Tyr755=) c.1845C>T (p.Tyr615=) n.2733C>T c.1062C>T (p.Tyr354=) c.2256C>T (p.Tyr752=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724229G>C | CA373795022 | ROR2 | c.2265C>G (p.Tyr755Ter) c.1845C>G (p.Tyr615Ter) n.2733C>G c.1062C>G (p.Tyr354Ter) c.2256C>G (p.Tyr752Ter) | |
| 9 | g.91724229G= | CA1863922393 | ROR2 | c.2265C= (p.Tyr755=) c.1845C= (p.Tyr615=) n.2733C= c.1062C= (p.Tyr354=) c.2256C= (p.Tyr752=) | |
| 9 | g.91724229G>T | CA118705 | ROR2 | c.2265C>A (p.Tyr755Ter) c.1845C>A (p.Tyr615Ter) n.2733C>A c.1062C>A (p.Tyr354Ter) c.2256C>A (p.Tyr752Ter) | ClinVar dbSNP gnomAD v4 |
| 9 | g.91724230T>A | CA373795025 | ROR2 | c.2264A>T (p.Tyr755Phe) c.1844A>T (p.Tyr615Phe) n.2732A>T c.1061A>T (p.Tyr354Phe) c.2255A>T (p.Tyr752Phe) | |
| 9 | g.91724230T>C | CA373795027 | ROR2 | c.2264A>G (p.Tyr755Cys) c.1844A>G (p.Tyr615Cys) n.2732A>G c.1061A>G (p.Tyr354Cys) c.2255A>G (p.Tyr752Cys) | |
| 9 | g.91724230T>G | CA373795029 | ROR2 | c.2264A>C (p.Tyr755Ser) c.1844A>C (p.Tyr615Ser) n.2732A>C c.1061A>C (p.Tyr354Ser) c.2255A>C (p.Tyr752Ser) | |
| 9 | g.91724230dup | CA915947030 | ROR2 | c.2264dup (p.Tyr755Ter) c.1844dup (p.Tyr615Ter) n.2732dup c.1061dup (p.Tyr354Ter) c.2255dup (p.Tyr752Ter) | ClinVar dbSNP |
| 9 | g.91724231A>C | CA373795033 | ROR2 | c.2263T>G (p.Tyr755Asp) c.1843T>G (p.Tyr615Asp) n.2731T>G c.1060T>G (p.Tyr354Asp) c.2254T>G (p.Tyr752Asp) | gnomAD v4 |
| 9 | g.91724231A>G | CA373795043 | ROR2 | c.2263T>C (p.Tyr755His) c.1843T>C (p.Tyr615His) n.2731T>C c.1060T>C (p.Tyr354His) c.2254T>C (p.Tyr752His) | |
| 9 | g.91724231A>T | CA373795045 | ROR2 | c.2263T>A (p.Tyr755Asn) c.1843T>A (p.Tyr615Asn) n.2731T>A c.1060T>A (p.Tyr354Asn) c.2254T>A (p.Tyr752Asn) | |
| 9 | g.91724232G>A | CA466339129 | ROR2 | c.2262C>T (p.Asn754=) c.1842C>T (p.Asn614=) n.2730C>T c.1059C>T (p.Asn353=) c.2253C>T (p.Asn751=) | gnomAD v4 |
| 9 | g.91724232G>C | CA373795048 | ROR2 | c.2262C>G (p.Asn754Lys) c.1842C>G (p.Asn614Lys) n.2730C>G c.1059C>G (p.Asn353Lys) c.2253C>G (p.Asn751Lys) | |
| 9 | g.91724232G>T | CA373795049 | ROR2 | c.2262C>A (p.Asn754Lys) c.1842C>A (p.Asn614Lys) n.2730C>A c.1059C>A (p.Asn353Lys) c.2253C>A (p.Asn751Lys) | |
| 9 | g.91724233T>A | CA373795050 | ROR2 | c.2261A>T (p.Asn754Ile) c.1841A>T (p.Asn614Ile) n.2729A>T c.1058A>T (p.Asn353Ile) c.2252A>T (p.Asn751Ile) | |
| 9 | g.91724233T>C | CA373795051 | ROR2 | c.2261A>G (p.Asn754Ser) c.1841A>G (p.Asn614Ser) n.2729A>G c.1058A>G (p.Asn353Ser) c.2252A>G (p.Asn751Ser) | |
| 9 | g.91724233T>G | CA373795052 | ROR2 | c.2261A>C (p.Asn754Thr) c.1841A>C (p.Asn614Thr) n.2729A>C c.1058A>C (p.Asn353Thr) c.2252A>C (p.Asn751Thr) | |
| 9 | g.91724234T>A | CA373795053 | ROR2 | c.2260A>T (p.Asn754Tyr) c.1840A>T (p.Asn614Tyr) n.2728A>T c.1057A>T (p.Asn353Tyr) c.2251A>T (p.Asn751Tyr) | gnomAD v4 |
| 9 | g.91724234T>C | CA373795056 | ROR2 | c.2260A>G (p.Asn754Asp) c.1840A>G (p.Asn614Asp) n.2728A>G c.1057A>G (p.Asn353Asp) c.2251A>G (p.Asn751Asp) | dbSNP |
| 9 | g.91724234T>G | CA373795055 | ROR2 | c.2260A>C (p.Asn754His) c.1840A>C (p.Asn614His) n.2728A>C c.1057A>C (p.Asn353His) c.2251A>C (p.Asn751His) | |
| 9 | g.91724234T= | CA1863922400 | ROR2 | c.2260A= (p.Asn754=) c.1840A= (p.Asn614=) n.2728A= c.1057A= (p.Asn353=) c.2251A= (p.Asn751=) | |
| 9 | g.91724235G>A | CA466339132 | ROR2 | c.2259C>T (p.Ser753=) c.1839C>T (p.Ser613=) n.2727C>T c.1056C>T (p.Ser352=) c.2250C>T (p.Ser750=) | dbSNP |
| 9 | g.91724235G>C | CA466339133 | ROR2 | c.2259C>G (p.Ser753=) c.1839C>G (p.Ser613=) n.2727C>G c.1056C>G (p.Ser352=) c.2250C>G (p.Ser750=) | |
| 9 | g.91724235G= | CA1863922402 | ROR2 | c.2259C= (p.Ser753=) c.1839C= (p.Ser613=) n.2727C= c.1056C= (p.Ser352=) c.2250C= (p.Ser750=) | |
| 9 | g.91724235G>T | CA466339134 | ROR2 | c.2259C>A (p.Ser753=) c.1839C>A (p.Ser613=) n.2727C>A c.1056C>A (p.Ser352=) c.2250C>A (p.Ser750=) | |
| 9 | g.91724236G>A | CA373795058 | ROR2 | c.2258C>T (p.Ser753Phe) c.1838C>T (p.Ser613Phe) n.2726C>T c.1055C>T (p.Ser352Phe) c.2249C>T (p.Ser750Phe) | |
| 9 | g.91724236G>C | CA373795062 | ROR2 | c.2258C>G (p.Ser753Cys) c.1838C>G (p.Ser613Cys) n.2726C>G c.1055C>G (p.Ser352Cys) c.2249C>G (p.Ser750Cys) | gnomAD v4 |
| 9 | g.91724236G>T | CA373795060 | ROR2 | c.2258C>A (p.Ser753Tyr) c.1838C>A (p.Ser613Tyr) n.2726C>A c.1055C>A (p.Ser352Tyr) c.2249C>A (p.Ser750Tyr) | |
| 9 | g.91724237A>C | CA373795064 | ROR2 | c.2257T>G (p.Ser753Ala) c.1837T>G (p.Ser613Ala) n.2725T>G c.1054T>G (p.Ser352Ala) c.2248T>G (p.Ser750Ala) | |
| 9 | g.91724237A>G | CA373795066 | ROR2 | c.2257T>C (p.Ser753Pro) c.1837T>C (p.Ser613Pro) n.2725T>C c.1054T>C (p.Ser352Pro) c.2248T>C (p.Ser750Pro) | |
| 9 | g.91724237A>T | CA373795069 | ROR2 | c.2257T>A (p.Ser753Thr) c.1837T>A (p.Ser613Thr) n.2725T>A c.1054T>A (p.Ser352Thr) c.2248T>A (p.Ser750Thr) | |
| 9 | g.91724238A>C | CA466339135 | ROR2 | c.2256T>G (p.Leu752=) c.1836T>G (p.Leu612=) n.2724T>G c.1053T>G (p.Leu351=) c.2247T>G (p.Leu749=) | |
| 9 | g.91724238A>G | CA466339136 | ROR2 | c.2256T>C (p.Leu752=) c.1836T>C (p.Leu612=) n.2724T>C c.1053T>C (p.Leu351=) c.2247T>C (p.Leu749=) | |
| 9 | g.91724238A>T | CA466339137 | ROR2 | c.2256T>A (p.Leu752=) c.1836T>A (p.Leu612=) n.2724T>A c.1053T>A (p.Leu351=) c.2247T>A (p.Leu749=) | |
| 9 | g.91724239A= | CA1863922406 | ROR2 | c.2255T= (p.Leu752=) c.1835T= (p.Leu612=) n.2723T= c.1052T= (p.Leu351=) c.2246T= (p.Leu749=) | |
| 9 | g.91724239A>C | CA373795073 | ROR2 | c.2255T>G (p.Leu752Arg) c.1835T>G (p.Leu612Arg) n.2723T>G c.1052T>G (p.Leu351Arg) c.2246T>G (p.Leu749Arg) | |
| 9 | g.91724239A>G | CA5120437 | ROR2 | c.2255T>C (p.Leu752Pro) c.1835T>C (p.Leu612Pro) n.2723T>C c.1052T>C (p.Leu351Pro) c.2246T>C (p.Leu749Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724239A>T | CA373795076 | ROR2 | c.2255T>A (p.Leu752His) c.1835T>A (p.Leu612His) n.2723T>A c.1052T>A (p.Leu351His) c.2246T>A (p.Leu749His) | |
| 9 | g.91724240G>A | CA373795078 | ROR2 | c.2254C>T (p.Leu752Phe) c.1834C>T (p.Leu612Phe) n.2722C>T c.1051C>T (p.Leu351Phe) c.2245C>T (p.Leu749Phe) | |
| 9 | g.91724240G>C | CA373795080 | ROR2 | c.2254C>G (p.Leu752Val) c.1834C>G (p.Leu612Val) n.2722C>G c.1051C>G (p.Leu351Val) c.2245C>G (p.Leu749Val) | |
| 9 | g.91724240G>T | CA373795083 | ROR2 | c.2254C>A (p.Leu752Ile) c.1834C>A (p.Leu612Ile) n.2722C>A c.1051C>A (p.Leu351Ile) c.2245C>A (p.Leu749Ile) | gnomAD v4 |
| 9 | g.91724241del | CA2582341998 | ROR2 | c.2254del (p.Leu752PhefsTer22) c.1834del (p.Leu612PhefsTer22) n.2722del c.1051del (p.Leu351PhefsTer22) c.2245del (p.Leu749PhefsTer22) | ClinVar |
| 9 | g.91724241G>A | CA466339138 | ROR2 | c.2253C>T (p.Asn751=) c.1833C>T (p.Asn611=) n.2721C>T c.1050C>T (p.Asn350=) c.2244C>T (p.Asn748=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724241G>C | CA373795084 | ROR2 | c.2253C>G (p.Asn751Lys) c.1833C>G (p.Asn611Lys) n.2721C>G c.1050C>G (p.Asn350Lys) c.2244C>G (p.Asn748Lys) | |
| 9 | g.91724241G= | CA1863922409 | ROR2 | c.2253C= (p.Asn751=) c.1833C= (p.Asn611=) n.2721C= c.1050C= (p.Asn350=) c.2244C= (p.Asn748=) | |
| 9 | g.91724241G>T | CA373795085 | ROR2 | c.2253C>A (p.Asn751Lys) c.1833C>A (p.Asn611Lys) n.2721C>A c.1050C>A (p.Asn350Lys) c.2244C>A (p.Asn748Lys) | |
| 9 | g.91724242T>A | CA373795088 | ROR2 | c.2252A>T (p.Asn751Ile) c.1832A>T (p.Asn611Ile) n.2720A>T c.1049A>T (p.Asn350Ile) c.2243A>T (p.Asn748Ile) | |
| 9 | g.91724242T>C | CA373795086 | ROR2 | c.2252A>G (p.Asn751Ser) c.1832A>G (p.Asn611Ser) n.2720A>G c.1049A>G (p.Asn350Ser) c.2243A>G (p.Asn748Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724242T>G | CA373795087 | ROR2 | c.2252A>C (p.Asn751Thr) c.1832A>C (p.Asn611Thr) n.2720A>C c.1049A>C (p.Asn350Thr) c.2243A>C (p.Asn748Thr) | |
| 9 | g.91724242T= | CA1863922414 | ROR2 | c.2252A= (p.Asn751=) c.1832A= (p.Asn611=) n.2720A= c.1049A= (p.Asn350=) c.2243A= (p.Asn748=) | |
| 9 | g.91724243T>A | CA373795090 | ROR2 | c.2251A>T (p.Asn751Tyr) c.1831A>T (p.Asn611Tyr) n.2719A>T c.1048A>T (p.Asn350Tyr) c.2242A>T (p.Asn748Tyr) | |
| 9 | g.91724243T>C | CA5120438 | ROR2 | c.2251A>G (p.Asn751Asp) c.1831A>G (p.Asn611Asp) n.2719A>G c.1048A>G (p.Asn350Asp) c.2242A>G (p.Asn748Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724243T>G | CA373795094 | ROR2 | c.2251A>C (p.Asn751His) c.1831A>C (p.Asn611His) n.2719A>C c.1048A>C (p.Asn350His) c.2242A>C (p.Asn748His) | |
| 9 | g.91724243T= | CA1863922417 | ROR2 | c.2251A= (p.Asn751=) c.1831A= (p.Asn611=) n.2719A= c.1048A= (p.Asn350=) c.2242A= (p.Asn748=) | |
| 9 | g.91724244G>A | CA466339139 | ROR2 | c.2250C>T (p.Gly750=) c.1830C>T (p.Gly610=) n.2718C>T c.1047C>T (p.Gly349=) c.2241C>T (p.Gly747=) | dbSNP COSMIC |
| 9 | g.91724244G>C | CA466339140 | ROR2 | c.2250C>G (p.Gly750=) c.1830C>G (p.Gly610=) n.2718C>G c.1047C>G (p.Gly349=) c.2241C>G (p.Gly747=) | |
| 9 | g.91724244G>T | CA466339141 | ROR2 | c.2250C>A (p.Gly750=) c.1830C>A (p.Gly610=) n.2718C>A c.1047C>A (p.Gly349=) c.2241C>A (p.Gly747=) | |
| 9 | g.91724244_91724245delinsGC | CA1863922421 | ROR2 | c.2249_2250delinsGC (p.Gly750=) c.1829_1830delinsGC (p.Gly610=) n.2717_2718delinsGC c.1046_1047delinsGC (p.Gly349=) c.2240_2241delinsGC (p.Gly747=) | |
| 9 | g.91724245C>A | CA5120440 | ROR2 | c.2249G>T (p.Gly750Val) c.1829G>T (p.Gly610Val) n.2717G>T c.1046G>T (p.Gly349Val) c.2240G>T (p.Gly747Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724245C= | CA1863922428 | ROR2 | c.2249G= (p.Gly750=) c.1829G= (p.Gly610=) n.2717G= c.1046G= (p.Gly349=) c.2240G= (p.Gly747=) | |
| 9 | g.91724245C>G | CA373795098 | ROR2 | c.2249G>C (p.Gly750Ala) c.1829G>C (p.Gly610Ala) n.2717G>C c.1046G>C (p.Gly349Ala) c.2240G>C (p.Gly747Ala) | |
| 9 | g.91724245C>T | CA5120439 | ROR2 | c.2249G>A (p.Gly750Asp) c.1829G>A (p.Gly610Asp) n.2717G>A c.1046G>A (p.Gly349Asp) c.2240G>A (p.Gly747Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724248del | CA278867 | ROR2 | c.2249del (p.Gly750AlafsTer24) c.1829del (p.Gly610AlafsTer24) n.2717del c.1046del (p.Gly349AlafsTer24) c.2240del (p.Gly747AlafsTer24) | ClinVar dbSNP gnomAD v4 |
| 9 | g.91724246C>A | CA373795102 | ROR2 | c.2248G>T (p.Gly750Cys) c.1828G>T (p.Gly610Cys) n.2716G>T c.1045G>T (p.Gly349Cys) c.2239G>T (p.Gly747Cys) | |
| 9 | g.91724246C>G | CA373795103 | ROR2 | c.2248G>C (p.Gly750Arg) c.1828G>C (p.Gly610Arg) n.2716G>C c.1045G>C (p.Gly349Arg) c.2239G>C (p.Gly747Arg) | |
| 9 | g.91724246C>T | CA373795106 | ROR2 | c.2248G>A (p.Gly750Ser) c.1828G>A (p.Gly610Ser) n.2716G>A c.1045G>A (p.Gly349Ser) c.2239G>A (p.Gly747Ser) | |
| 9 | g.91724247C>A | CA373795109 | ROR2 | c.2247G>T (p.Trp749Cys) c.1827G>T (p.Trp609Cys) n.2715G>T c.1044G>T (p.Trp348Cys) c.2238G>T (p.Trp746Cys) | |
| 9 | g.91724247C= | CA1863922431 | ROR2 | c.2247G= (p.Trp749=) c.1827G= (p.Trp609=) n.2715G= c.1044G= (p.Trp348=) c.2238G= (p.Trp746=) | |
| 9 | g.91724247C>G | CA373795110 | ROR2 | c.2247G>C (p.Trp749Cys) c.1827G>C (p.Trp609Cys) n.2715G>C c.1044G>C (p.Trp348Cys) c.2238G>C (p.Trp746Cys) | |
| 9 | g.91724247C>T | CA118709 | ROR2 | c.2247G>A (p.Trp749Ter) c.1827G>A (p.Trp609Ter) n.2715G>A c.1044G>A (p.Trp348Ter) c.2238G>A (p.Trp746Ter) | ClinVar dbSNP |
| 9 | g.91724248C>A | CA373795111 | ROR2 | c.2246G>T (p.Trp749Leu) c.1826G>T (p.Trp609Leu) n.2714G>T c.1043G>T (p.Trp348Leu) c.2237G>T (p.Trp746Leu) | |
| 9 | g.91724248C= | CA1863922439 | ROR2 | c.2246G= (p.Trp749=) c.1826G= (p.Trp609=) n.2714G= c.1043G= (p.Trp348=) c.2237G= (p.Trp746=) | |
| 9 | g.91724248C>G | CA373795112 | ROR2 | c.2246G>C (p.Trp749Ser) c.1826G>C (p.Trp609Ser) n.2714G>C c.1043G>C (p.Trp348Ser) c.2237G>C (p.Trp746Ser) | |
| 9 | g.91724248C>T | CA118707 | ROR2 | c.2246G>A (p.Trp749Ter) c.1826G>A (p.Trp609Ter) n.2714G>A c.1043G>A (p.Trp348Ter) c.2237G>A (p.Trp746Ter) | ClinVar dbSNP |