Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.91723691C>A | CA373793048 | ROR2 | c.2803G>T (p.Asp935Tyr) c.1920+463G>T (n.1920+463G>T) n.3271G>T c.2383G>T (p.Asp795Tyr) c.1600G>T (p.Asp534Tyr) c.2794G>T (p.Asp932Tyr) | |
9 | g.91723691C= | CA1863921376 | ROR2 | c.2803G= (p.Asp935=) c.1920+463G= (n.1920+463G=) n.3271G= c.2383G= (p.Asp795=) c.1600G= (p.Asp534=) c.2794G= (p.Asp932=) | |
9 | g.91723691C>G | CA373793049 | ROR2 | c.2803G>C (p.Asp935His) c.1920+463G>C (n.1920+463G>C) n.3271G>C c.2383G>C (p.Asp795His) c.1600G>C (p.Asp534His) c.2794G>C (p.Asp932His) | |
9 | g.91723691C>T | CA373793050 | ROR2 | c.2803G>A (p.Asp935Asn) c.1920+463G>A (n.1920+463G>A) n.3271G>A c.2383G>A (p.Asp795Asn) c.1600G>A (p.Asp534Asn) c.2794G>A (p.Asp932Asn) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723692C>A | CA465995389 | ROR2 | c.2802G>T (p.Val934=) c.1920+462G>T (n.1920+462G>T) n.3270G>T c.2382G>T (p.Val794=) c.1599G>T (p.Val533=) c.2793G>T (p.Val931=) | |
9 | g.91723692C= | CA1863921379 | ROR2 | c.2802G= (p.Val934=) c.1920+462G= (n.1920+462G=) n.3270G= c.2382G= (p.Val794=) c.1599G= (p.Val533=) c.2793G= (p.Val931=) | |
9 | g.91723692C>G | CA465995390 | ROR2 | c.2802G>C (p.Val934=) c.1920+462G>C (n.1920+462G>C) n.3270G>C c.2382G>C (p.Val794=) c.1599G>C (p.Val533=) c.2793G>C (p.Val931=) | |
9 | g.91723692C>T | CA465995391 | ROR2 | c.2802G>A (p.Val934=) c.1920+462G>A (n.1920+462G>A) n.3270G>A c.2382G>A (p.Val794=) c.1599G>A (p.Val533=) c.2793G>A (p.Val931=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723693A>C | CA373793051 | ROR2 | c.2801T>G (p.Val934Gly) c.1920+461T>G (n.1920+461T>G) n.3269T>G c.2381T>G (p.Val794Gly) c.1598T>G (p.Val533Gly) c.2792T>G (p.Val931Gly) | |
9 | g.91723693A>G | CA373793052 | ROR2 | c.2801T>C (p.Val934Ala) c.1920+461T>C (n.1920+461T>C) n.3269T>C c.2381T>C (p.Val794Ala) c.1598T>C (p.Val533Ala) c.2792T>C (p.Val931Ala) | |
9 | g.91723693A>T | CA373793053 | ROR2 | c.2801T>A (p.Val934Glu) c.1920+461T>A (n.1920+461T>A) n.3269T>A c.2381T>A (p.Val794Glu) c.1598T>A (p.Val533Glu) c.2792T>A (p.Val931Glu) | |
9 | g.91723694C>A | CA5120308 | ROR2 | c.2800G>T (p.Val934Leu) c.1920+460G>T (n.1920+460G>T) n.3268G>T c.2380G>T (p.Val794Leu) c.1597G>T (p.Val533Leu) c.2791G>T (p.Val931Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91723694C= | CA1863921382 | ROR2 | c.2800G= (p.Val934=) c.1920+460G= (n.1920+460G=) n.3268G= c.2380G= (p.Val794=) c.1597G= (p.Val533=) c.2791G= (p.Val931=) | |
9 | g.91723694C>G | CA373793055 | ROR2 | c.2800G>C (p.Val934Leu) c.1920+460G>C (n.1920+460G>C) n.3268G>C c.2380G>C (p.Val794Leu) c.1597G>C (p.Val533Leu) c.2791G>C (p.Val931Leu) | |
9 | g.91723694C>T | CA373793054 | ROR2 | c.2800G>A (p.Val934Met) c.1920+460G>A (n.1920+460G>A) n.3268G>A c.2380G>A (p.Val794Met) c.1597G>A (p.Val533Met) c.2791G>A (p.Val931Met) | |
9 | g.91723695C>A | CA373793057 | ROR2 | c.2799G>T (p.Gln933His) c.1920+459G>T (n.1920+459G>T) n.3267G>T c.2379G>T (p.Gln793His) c.1596G>T (p.Gln532His) c.2790G>T (p.Gln930His) | |
9 | g.91723695C>G | CA373793056 | ROR2 | c.2799G>C (p.Gln933His) c.1920+459G>C (n.1920+459G>C) n.3267G>C c.2379G>C (p.Gln793His) c.1596G>C (p.Gln532His) c.2790G>C (p.Gln930His) | |
9 | g.91723695C>T | CA465995393 | ROR2 | c.2799G>A (p.Gln933=) c.1920+459G>A (n.1920+459G>A) n.3267G>A c.2379G>A (p.Gln793=) c.1596G>A (p.Gln532=) c.2790G>A (p.Gln930=) | |
9 | g.91723696T>A | CA373793058 | ROR2 | c.2798A>T (p.Gln933Leu) c.1920+458A>T (n.1920+458A>T) n.3266A>T c.2378A>T (p.Gln793Leu) c.1595A>T (p.Gln532Leu) c.2789A>T (p.Gln930Leu) | |
9 | g.91723696T>C | CA195321353 | ROR2 | c.2798A>G (p.Gln933Arg) c.1920+458A>G (n.1920+458A>G) n.3266A>G c.2378A>G (p.Gln793Arg) c.1595A>G (p.Gln532Arg) c.2789A>G (p.Gln930Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723696T>G | CA373793059 | ROR2 | c.2798A>C (p.Gln933Pro) c.1920+458A>C (n.1920+458A>C) n.3266A>C c.2378A>C (p.Gln793Pro) c.1595A>C (p.Gln532Pro) c.2789A>C (p.Gln930Pro) | |
9 | g.91723696T= | CA1863921385 | ROR2 | c.2798A= (p.Gln933=) c.1920+458A= (n.1920+458A=) n.3266A= c.2378A= (p.Gln793=) c.1595A= (p.Gln532=) c.2789A= (p.Gln930=) | |
9 | g.91723697G>A | CA373793060 | ROR2 | c.2797C>T (p.Gln933Ter) c.1920+457C>T (n.1920+457C>T) n.3265C>T c.2377C>T (p.Gln793Ter) c.1594C>T (p.Gln532Ter) c.2788C>T (p.Gln930Ter) | gnomAD v4 |
9 | g.91723697G>C | CA373793061 | ROR2 | c.2797C>G (p.Gln933Glu) c.1920+457C>G (n.1920+457C>G) n.3265C>G c.2377C>G (p.Gln793Glu) c.1594C>G (p.Gln532Glu) c.2788C>G (p.Gln930Glu) | |
9 | g.91723697G>T | CA373793062 | ROR2 | c.2797C>A (p.Gln933Lys) c.1920+457C>A (n.1920+457C>A) n.3265C>A c.2377C>A (p.Gln793Lys) c.1594C>A (p.Gln532Lys) c.2788C>A (p.Gln930Lys) | |
9 | g.91723698C>A | CA465995395 | ROR2 | c.2796G>T (p.Leu932=) c.1920+456G>T (n.1920+456G>T) n.3264G>T c.2376G>T (p.Leu792=) c.1593G>T (p.Leu531=) c.2787G>T (p.Leu929=) | |
9 | g.91723698C>G | CA465995396 | ROR2 | c.2796G>C (p.Leu932=) c.1920+456G>C (n.1920+456G>C) n.3264G>C c.2376G>C (p.Leu792=) c.1593G>C (p.Leu531=) c.2787G>C (p.Leu929=) | |
9 | g.91723698C>T | CA465995397 | ROR2 | c.2796G>A (p.Leu932=) c.1920+456G>A (n.1920+456G>A) n.3264G>A c.2376G>A (p.Leu792=) c.1593G>A (p.Leu531=) c.2787G>A (p.Leu929=) | |
9 | g.91723698_91723700delinsCAG | CA1863921391 | ROR2 | c.2794_2796delinsCTG (p.Leu932=) c.1920+454_1920+456delinsCTG (n.1920+454_1920+456delinsCTG) n.3262_3264delinsCTG c.2374_2376delinsCTG (p.Leu792=) c.1591_1593delinsCTG (p.Leu531=) c.2785_2787delinsCTG (p.Leu929=) | |
9 | g.91723699A= | CA1863921397 | ROR2 | c.2795T= (p.Leu932=) c.1920+455T= (n.1920+455T=) n.3263T= c.2375T= (p.Leu792=) c.1592T= (p.Leu531=) c.2786T= (p.Leu929=) | |
9 | g.91723699A>C | CA373793063 | ROR2 | c.2795T>G (p.Leu932Arg) c.1920+455T>G (n.1920+455T>G) n.3263T>G c.2375T>G (p.Leu792Arg) c.1592T>G (p.Leu531Arg) c.2786T>G (p.Leu929Arg) | |
9 | g.91723699A>G | CA195321357 | ROR2 | c.2795T>C (p.Leu932Pro) c.1920+455T>C (n.1920+455T>C) n.3263T>C c.2375T>C (p.Leu792Pro) c.1592T>C (p.Leu531Pro) c.2786T>C (p.Leu929Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723699A>T | CA373793064 | ROR2 | c.2795T>A (p.Leu932Gln) c.1920+455T>A (n.1920+455T>A) n.3263T>A c.2375T>A (p.Leu792Gln) c.1592T>A (p.Leu531Gln) c.2786T>A (p.Leu929Gln) | |
9 | g.91723701_91723702del | CA5120309 | ROR2 | c.2794_2795del (p.Leu932AlafsTer?) c.1920+454_1920+455del (n.1920+454_1920+455del) n.3262_3263del c.2374_2375del (p.Leu792AlafsTer?) c.1591_1592del (p.Leu531AlafsTer?) c.2785_2786del (p.Leu929AlafsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723700G>A | CA465995402 | ROR2 | c.2794C>T (p.Leu932=) c.1920+454C>T (n.1920+454C>T) n.3262C>T c.2374C>T (p.Leu792=) c.1591C>T (p.Leu531=) c.2785C>T (p.Leu929=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91723700G>C | CA373793065 | ROR2 | c.2794C>G (p.Leu932Val) c.1920+454C>G (n.1920+454C>G) n.3262C>G c.2374C>G (p.Leu792Val) c.1591C>G (p.Leu531Val) c.2785C>G (p.Leu929Val) | |
9 | g.91723700G= | CA1863921401 | ROR2 | c.2794C= (p.Leu932=) c.1920+454C= (n.1920+454C=) n.3262C= c.2374C= (p.Leu792=) c.1591C= (p.Leu531=) c.2785C= (p.Leu929=) | |
9 | g.91723700G>T | CA373793066 | ROR2 | c.2794C>A (p.Leu932Met) c.1920+454C>A (n.1920+454C>A) n.3262C>A c.2374C>A (p.Leu792Met) c.1591C>A (p.Leu531Met) c.2785C>A (p.Leu929Met) | |
9 | g.91723701A>C | CA465995403 | ROR2 | c.2793T>G (p.Thr931=) c.1920+453T>G (n.1920+453T>G) n.3261T>G c.2373T>G (p.Thr791=) c.1590T>G (p.Thr530=) c.2784T>G (p.Thr928=) | |
9 | g.91723701A>G | CA465995404 | ROR2 | c.2793T>C (p.Thr931=) c.1920+453T>C (n.1920+453T>C) n.3261T>C c.2373T>C (p.Thr791=) c.1590T>C (p.Thr530=) c.2784T>C (p.Thr928=) | |
9 | g.91723701A>T | CA465995405 | ROR2 | c.2793T>A (p.Thr931=) c.1920+453T>A (n.1920+453T>A) n.3261T>A c.2373T>A (p.Thr791=) c.1590T>A (p.Thr530=) c.2784T>A (p.Thr928=) | dbSNP gnomAD v4 |
9 | g.91723702G>A | CA373793067 | ROR2 | c.2792C>T (p.Thr931Ile) c.1920+452C>T (n.1920+452C>T) n.3260C>T c.2372C>T (p.Thr791Ile) c.1589C>T (p.Thr530Ile) c.2783C>T (p.Thr928Ile) | gnomAD v4 |
9 | g.91723702G>C | CA373793069 | ROR2 | c.2792C>G (p.Thr931Ser) c.1920+452C>G (n.1920+452C>G) n.3260C>G c.2372C>G (p.Thr791Ser) c.1589C>G (p.Thr530Ser) c.2783C>G (p.Thr928Ser) | dbSNP |
9 | g.91723702G= | CA1863921405 | ROR2 | c.2792C= (p.Thr931=) c.1920+452C= (n.1920+452C=) n.3260C= c.2372C= (p.Thr791=) c.1589C= (p.Thr530=) c.2783C= (p.Thr928=) | |
9 | g.91723702G>T | CA373793068 | ROR2 | c.2792C>A (p.Thr931Asn) c.1920+452C>A (n.1920+452C>A) n.3260C>A c.2372C>A (p.Thr791Asn) c.1589C>A (p.Thr530Asn) c.2783C>A (p.Thr928Asn) | |
9 | g.91723703T>A | CA373793070 | ROR2 | c.2791A>T (p.Thr931Ser) c.1920+451A>T (n.1920+451A>T) n.3259A>T c.2371A>T (p.Thr791Ser) c.1588A>T (p.Thr530Ser) c.2782A>T (p.Thr928Ser) | |
9 | g.91723703T>C | CA5120310 | ROR2 | c.2791A>G (p.Thr931Ala) c.1920+451A>G (n.1920+451A>G) n.3259A>G c.2371A>G (p.Thr791Ala) c.1588A>G (p.Thr530Ala) c.2782A>G (p.Thr928Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723703T>G | CA373793071 | ROR2 | c.2791A>C (p.Thr931Pro) c.1920+451A>C (n.1920+451A>C) n.3259A>C c.2371A>C (p.Thr791Pro) c.1588A>C (p.Thr530Pro) c.2782A>C (p.Thr928Pro) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723703T= | CA1863921409 | ROR2 | c.2791A= (p.Thr931=) c.1920+451A= (n.1920+451A=) n.3259A= c.2371A= (p.Thr791=) c.1588A= (p.Thr530=) c.2782A= (p.Thr928=) | |
9 | g.91723704G>A | CA465995409 | ROR2 | c.2790C>T (p.Asp930=) c.1920+450C>T (n.1920+450C>T) n.3258C>T c.2370C>T (p.Asp790=) c.1587C>T (p.Asp529=) c.2781C>T (p.Asp927=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91723704G>C | CA373793072 | ROR2 | c.2790C>G (p.Asp930Glu) c.1920+450C>G (n.1920+450C>G) n.3258C>G c.2370C>G (p.Asp790Glu) c.1587C>G (p.Asp529Glu) c.2781C>G (p.Asp927Glu) | |
9 | g.91723704G= | CA1863921413 | ROR2 | c.2790C= (p.Asp930=) c.1920+450C= (n.1920+450C=) n.3258C= c.2370C= (p.Asp790=) c.1587C= (p.Asp529=) c.2781C= (p.Asp927=) | |
9 | g.91723704G>T | CA373793073 | ROR2 | c.2790C>A (p.Asp930Glu) c.1920+450C>A (n.1920+450C>A) n.3258C>A c.2370C>A (p.Asp790Glu) c.1587C>A (p.Asp529Glu) c.2781C>A (p.Asp927Glu) | |
9 | g.91723705T>A | CA373793074 | ROR2 | c.2789A>T (p.Asp930Val) c.1920+449A>T (n.1920+449A>T) n.3257A>T c.2369A>T (p.Asp790Val) c.1586A>T (p.Asp529Val) c.2780A>T (p.Asp927Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723705T>C | CA373793075 | ROR2 | c.2789A>G (p.Asp930Gly) c.1920+449A>G (n.1920+449A>G) n.3257A>G c.2369A>G (p.Asp790Gly) c.1586A>G (p.Asp529Gly) c.2780A>G (p.Asp927Gly) | |
9 | g.91723705T>G | CA373793076 | ROR2 | c.2789A>C (p.Asp930Ala) c.1920+449A>C (n.1920+449A>C) n.3257A>C c.2369A>C (p.Asp790Ala) c.1586A>C (p.Asp529Ala) c.2780A>C (p.Asp927Ala) | |
9 | g.91723705T= | CA1863921415 | ROR2 | c.2789A= (p.Asp930=) c.1920+449A= (n.1920+449A=) n.3257A= c.2369A= (p.Asp790=) c.1586A= (p.Asp529=) c.2780A= (p.Asp927=) | |
9 | g.91723706C>A | CA373793077 | ROR2 | c.2788G>T (p.Asp930Tyr) c.1920+448G>T (n.1920+448G>T) n.3256G>T c.2368G>T (p.Asp790Tyr) c.1585G>T (p.Asp529Tyr) c.2779G>T (p.Asp927Tyr) | |
9 | g.91723706C>G | CA373793078 | ROR2 | c.2788G>C (p.Asp930His) c.1920+448G>C (n.1920+448G>C) n.3256G>C c.2368G>C (p.Asp790His) c.1585G>C (p.Asp529His) c.2779G>C (p.Asp927His) | |
9 | g.91723706C>T | CA373793079 | ROR2 | c.2788G>A (p.Asp930Asn) c.1920+448G>A (n.1920+448G>A) n.3256G>A c.2368G>A (p.Asp790Asn) c.1585G>A (p.Asp529Asn) c.2779G>A (p.Asp927Asn) | |
9 | g.91723707A>C | CA373793081 | ROR2 | c.2787T>G (p.Cys929Trp) c.1920+447T>G (n.1920+447T>G) n.3255T>G c.2367T>G (p.Cys789Trp) c.1584T>G (p.Cys528Trp) c.2778T>G (p.Cys926Trp) | |
9 | g.91723707A>G | CA465995413 | ROR2 | c.2787T>C (p.Cys929=) c.1920+447T>C (n.1920+447T>C) n.3255T>C c.2367T>C (p.Cys789=) c.1584T>C (p.Cys528=) c.2778T>C (p.Cys926=) | |
9 | g.91723707A>T | CA373793080 | ROR2 | c.2787T>A (p.Cys929Ter) c.1920+447T>A (n.1920+447T>A) n.3255T>A c.2367T>A (p.Cys789Ter) c.1584T>A (p.Cys528Ter) c.2778T>A (p.Cys926Ter) | |
9 | g.91723708C>A | CA373793082 | ROR2 | c.2786G>T (p.Cys929Phe) c.1920+446G>T (n.1920+446G>T) n.3254G>T c.2366G>T (p.Cys789Phe) c.1583G>T (p.Cys528Phe) c.2777G>T (p.Cys926Phe) | |
9 | g.91723708C= | CA1863921418 | ROR2 | c.2786G= (p.Cys929=) c.1920+446G= (n.1920+446G=) n.3254G= c.2366G= (p.Cys789=) c.1583G= (p.Cys528=) c.2777G= (p.Cys926=) | |
9 | g.91723708C>G | CA5120311 | ROR2 | c.2786G>C (p.Cys929Ser) c.1920+446G>C (n.1920+446G>C) n.3254G>C c.2366G>C (p.Cys789Ser) c.1583G>C (p.Cys528Ser) c.2777G>C (p.Cys926Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723708C>T | CA373793083 | ROR2 | c.2786G>A (p.Cys929Tyr) c.1920+446G>A (n.1920+446G>A) n.3254G>A c.2366G>A (p.Cys789Tyr) c.1583G>A (p.Cys528Tyr) c.2777G>A (p.Cys926Tyr) | |
9 | g.91723709A= | CA1863921421 | ROR2 | c.2785T= (p.Cys929=) c.1920+445T= (n.1920+445T=) n.3253T= c.2365T= (p.Cys789=) c.1582T= (p.Cys528=) c.2776T= (p.Cys926=) | |
9 | g.91723709A>C | CA373793084 | ROR2 | c.2785T>G (p.Cys929Gly) c.1920+445T>G (n.1920+445T>G) n.3253T>G c.2365T>G (p.Cys789Gly) c.1582T>G (p.Cys528Gly) c.2776T>G (p.Cys926Gly) | |
9 | g.91723709A>G | CA5120312 | ROR2 | c.2785T>C (p.Cys929Arg) c.1920+445T>C (n.1920+445T>C) n.3253T>C c.2365T>C (p.Cys789Arg) c.1582T>C (p.Cys528Arg) c.2776T>C (p.Cys926Arg) | ClinVar dbSNP ExAC gnomAD v2 |
9 | g.91723709A>T | CA373793085 | ROR2 | c.2785T>A (p.Cys929Ser) c.1920+445T>A (n.1920+445T>A) n.3253T>A c.2365T>A (p.Cys789Ser) c.1582T>A (p.Cys528Ser) c.2776T>A (p.Cys926Ser) | |
9 | g.91723710G>A | CA465995417 | ROR2 | c.2784C>T (p.Asp928=) c.1920+444C>T (n.1920+444C>T) n.3252C>T c.2364C>T (p.Asp788=) c.1581C>T (p.Asp527=) c.2775C>T (p.Asp925=) | gnomAD v4 |
9 | g.91723710G>C | CA373793086 | ROR2 | c.2784C>G (p.Asp928Glu) c.1920+444C>G (n.1920+444C>G) n.3252C>G c.2364C>G (p.Asp788Glu) c.1581C>G (p.Asp527Glu) c.2775C>G (p.Asp925Glu) | |
9 | g.91723710G>T | CA373793087 | ROR2 | c.2784C>A (p.Asp928Glu) c.1920+444C>A (n.1920+444C>A) n.3252C>A c.2364C>A (p.Asp788Glu) c.1581C>A (p.Asp527Glu) c.2775C>A (p.Asp925Glu) | |
9 | g.91723711T>A | CA373793088 | ROR2 | c.2783A>T (p.Asp928Val) c.1920+443A>T (n.1920+443A>T) n.3251A>T c.2363A>T (p.Asp788Val) c.1580A>T (p.Asp527Val) c.2774A>T (p.Asp925Val) | |
9 | g.91723711T>C | CA373793089 | ROR2 | c.2783A>G (p.Asp928Gly) c.1920+443A>G (n.1920+443A>G) n.3251A>G c.2363A>G (p.Asp788Gly) c.1580A>G (p.Asp527Gly) c.2774A>G (p.Asp925Gly) | |
9 | g.91723711T>G | CA373793090 | ROR2 | c.2783A>C (p.Asp928Ala) c.1920+443A>C (n.1920+443A>C) n.3251A>C c.2363A>C (p.Asp788Ala) c.1580A>C (p.Asp527Ala) c.2774A>C (p.Asp925Ala) | |
9 | g.91723711_91723712delinsTC | CA1863921425 | ROR2 | c.2782_2783delinsGA (p.Asp928=) c.1920+442_1920+443delinsGA (n.1920+442_1920+443delinsGA) n.3250_3251delinsGA c.2362_2363delinsGA (p.Asp788=) c.1579_1580delinsGA (p.Asp527=) c.2773_2774delinsGA (p.Asp925=) | |
9 | g.91723712C>A | CA373793091 | ROR2 | c.2782G>T (p.Asp928Tyr) c.1920+442G>T (n.1920+442G>T) n.3250G>T c.2362G>T (p.Asp788Tyr) c.1579G>T (p.Asp527Tyr) c.2773G>T (p.Asp925Tyr) | |
9 | g.91723712C= | CA1863921430 | ROR2 | c.2782G= (p.Asp928=) c.1920+442G= (n.1920+442G=) n.3250G= c.2362G= (p.Asp788=) c.1579G= (p.Asp527=) c.2773G= (p.Asp925=) | |
9 | g.91723712C>G | CA5120313 | ROR2 | c.2782G>C (p.Asp928His) c.1920+442G>C (n.1920+442G>C) n.3250G>C c.2362G>C (p.Asp788His) c.1579G>C (p.Asp527His) c.2773G>C (p.Asp925His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723712C>T | CA373793092 | ROR2 | c.2782G>A (p.Asp928Asn) c.1920+442G>A (n.1920+442G>A) n.3250G>A c.2362G>A (p.Asp788Asn) c.1579G>A (p.Asp527Asn) c.2773G>A (p.Asp925Asn) | ClinVar dbSNP gnomAD v4 |
9 | g.91723716del | CA589155667 | ROR2 | c.2782del (p.Asp928ThrfsTer?) c.1920+442del (n.1920+442del) n.3250del c.2362del (p.Asp788ThrfsTer?) c.1579del (p.Asp527ThrfsTer?) c.2773del (p.Asp925ThrfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723713C>A | CA465995422 | ROR2 | c.2781G>T (p.Gly927=) c.1920+441G>T (n.1920+441G>T) n.3249G>T c.2361G>T (p.Gly787=) c.1578G>T (p.Gly526=) c.2772G>T (p.Gly924=) | |
9 | g.91723713C>G | CA465995423 | ROR2 | c.2781G>C (p.Gly927=) c.1920+441G>C (n.1920+441G>C) n.3249G>C c.2361G>C (p.Gly787=) c.1578G>C (p.Gly526=) c.2772G>C (p.Gly924=) | |
9 | g.91723713C>T | CA465995424 | ROR2 | c.2781G>A (p.Gly927=) c.1920+441G>A (n.1920+441G>A) n.3249G>A c.2361G>A (p.Gly787=) c.1578G>A (p.Gly526=) c.2772G>A (p.Gly924=) | |
9 | g.91723714C>A | CA373793095 | ROR2 | c.2780G>T (p.Gly927Val) c.1920+440G>T (n.1920+440G>T) n.3248G>T c.2360G>T (p.Gly787Val) c.1577G>T (p.Gly526Val) c.2771G>T (p.Gly924Val) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723714C= | CA1863921439 | ROR2 | c.2780G= (p.Gly927=) c.1920+440G= (n.1920+440G=) n.3248G= c.2360G= (p.Gly787=) c.1577G= (p.Gly526=) c.2771G= (p.Gly924=) | |
9 | g.91723714C>G | CA373793094 | ROR2 | c.2780G>C (p.Gly927Ala) c.1920+440G>C (n.1920+440G>C) n.3248G>C c.2360G>C (p.Gly787Ala) c.1577G>C (p.Gly526Ala) c.2771G>C (p.Gly924Ala) | |
9 | g.91723714C>T | CA373793093 | ROR2 | c.2780G>A (p.Gly927Glu) c.1920+440G>A (n.1920+440G>A) n.3248G>A c.2360G>A (p.Gly787Glu) c.1577G>A (p.Gly526Glu) c.2771G>A (p.Gly924Glu) | |
9 | g.91723715C>A | CA373793096 | ROR2 | c.2779G>T (p.Gly927Trp) c.1920+439G>T (n.1920+439G>T) n.3247G>T c.2359G>T (p.Gly787Trp) c.1576G>T (p.Gly526Trp) c.2770G>T (p.Gly924Trp) | |
9 | g.91723715C>G | CA373793097 | ROR2 | c.2779G>C (p.Gly927Arg) c.1920+439G>C (n.1920+439G>C) n.3247G>C c.2359G>C (p.Gly787Arg) c.1576G>C (p.Gly526Arg) c.2770G>C (p.Gly924Arg) | |
9 | g.91723715C>T | CA373793098 | ROR2 | c.2779G>A (p.Gly927Arg) c.1920+439G>A (n.1920+439G>A) n.3247G>A c.2359G>A (p.Gly787Arg) c.1576G>A (p.Gly526Arg) c.2770G>A (p.Gly924Arg) | |
9 | g.91723716C>A | CA465995427 | ROR2 | c.2778G>T (p.Leu926=) c.1920+438G>T (n.1920+438G>T) n.3246G>T c.2358G>T (p.Leu786=) c.1575G>T (p.Leu525=) c.2769G>T (p.Leu923=) | |
9 | g.91723716C>G | CA465995430 | ROR2 | c.2778G>C (p.Leu926=) c.1920+438G>C (n.1920+438G>C) n.3246G>C c.2358G>C (p.Leu786=) c.1575G>C (p.Leu525=) c.2769G>C (p.Leu923=) | |
9 | g.91723716C>T | CA465995428 | ROR2 | c.2778G>A (p.Leu926=) c.1920+438G>A (n.1920+438G>A) n.3246G>A c.2358G>A (p.Leu786=) c.1575G>A (p.Leu525=) c.2769G>A (p.Leu923=) | COSMIC |
9 | g.91723717A= | CA1863921441 | ROR2 | c.2777T= (p.Leu926=) c.1920+437T= (n.1920+437T=) n.3245T= c.2357T= (p.Leu786=) c.1574T= (p.Leu525=) c.2768T= (p.Leu923=) | |
9 | g.91723717A>C | CA373793099 | ROR2 | c.2777T>G (p.Leu926Arg) c.1920+437T>G (n.1920+437T>G) n.3245T>G c.2357T>G (p.Leu786Arg) c.1574T>G (p.Leu525Arg) c.2768T>G (p.Leu923Arg) | |
9 | g.91723717A>G | CA373793100 | ROR2 | c.2777T>C (p.Leu926Pro) c.1920+437T>C (n.1920+437T>C) n.3245T>C c.2357T>C (p.Leu786Pro) c.1574T>C (p.Leu525Pro) c.2768T>C (p.Leu923Pro) | |
9 | g.91723717A>T | CA373793101 | ROR2 | c.2777T>A (p.Leu926Gln) c.1920+437T>A (n.1920+437T>A) n.3245T>A c.2357T>A (p.Leu786Gln) c.1574T>A (p.Leu525Gln) c.2768T>A (p.Leu923Gln) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723718G>A | CA465995431 | ROR2 | c.2776C>T (p.Leu926=) c.1920+436C>T (n.1920+436C>T) n.3244C>T c.2356C>T (p.Leu786=) c.1573C>T (p.Leu525=) c.2767C>T (p.Leu923=) | |
9 | g.91723718G>C | CA373793102 | ROR2 | c.2776C>G (p.Leu926Val) c.1920+436C>G (n.1920+436C>G) n.3244C>G c.2356C>G (p.Leu786Val) c.1573C>G (p.Leu525Val) c.2767C>G (p.Leu923Val) | |
9 | g.91723718G>T | CA373793103 | ROR2 | c.2776C>A (p.Leu926Met) c.1920+436C>A (n.1920+436C>A) n.3244C>A c.2356C>A (p.Leu786Met) c.1573C>A (p.Leu525Met) c.2767C>A (p.Leu923Met) | |
9 | g.91723719C>A | CA465995432 | ROR2 | c.2775G>T (p.Leu925=) c.1920+435G>T (n.1920+435G>T) n.3243G>T c.2355G>T (p.Leu785=) c.1572G>T (p.Leu524=) c.2766G>T (p.Leu922=) | |
9 | g.91723719C= | CA1863921448 | ROR2 | c.2775G= (p.Leu925=) c.1920+435G= (n.1920+435G=) n.3243G= c.2355G= (p.Leu785=) c.1572G= (p.Leu524=) c.2766G= (p.Leu922=) | |
9 | g.91723719C>G | CA465995433 | ROR2 | c.2775G>C (p.Leu925=) c.1920+435G>C (n.1920+435G>C) n.3243G>C c.2355G>C (p.Leu785=) c.1572G>C (p.Leu524=) c.2766G>C (p.Leu922=) | |
9 | g.91723719C>T | CA465995434 | ROR2 | c.2775G>A (p.Leu925=) c.1920+435G>A (n.1920+435G>A) n.3243G>A c.2355G>A (p.Leu785=) c.1572G>A (p.Leu524=) c.2766G>A (p.Leu922=) | dbSNP gnomAD v4 |
9 | g.91723720A>C | CA373793104 | ROR2 | c.2774T>G (p.Leu925Arg) c.1920+434T>G (n.1920+434T>G) n.3242T>G c.2354T>G (p.Leu785Arg) c.1571T>G (p.Leu524Arg) c.2765T>G (p.Leu922Arg) | |
9 | g.91723720A>G | CA373793105 | ROR2 | c.2774T>C (p.Leu925Pro) c.1920+434T>C (n.1920+434T>C) n.3242T>C c.2354T>C (p.Leu785Pro) c.1571T>C (p.Leu524Pro) c.2765T>C (p.Leu922Pro) | |
9 | g.91723720A>T | CA373793106 | ROR2 | c.2774T>A (p.Leu925Gln) c.1920+434T>A (n.1920+434T>A) n.3242T>A c.2354T>A (p.Leu785Gln) c.1571T>A (p.Leu524Gln) c.2765T>A (p.Leu922Gln) | |
9 | g.91723721G>A | CA465995435 | ROR2 | c.2773C>T (p.Leu925=) c.1920+433C>T (n.1920+433C>T) n.3241C>T c.2353C>T (p.Leu785=) c.1570C>T (p.Leu524=) c.2764C>T (p.Leu922=) | |
9 | g.91723721G>C | CA373793107 | ROR2 | c.2773C>G (p.Leu925Val) c.1920+433C>G (n.1920+433C>G) n.3241C>G c.2353C>G (p.Leu785Val) c.1570C>G (p.Leu524Val) c.2764C>G (p.Leu922Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723721G= | CA1863921452 | ROR2 | c.2773C= (p.Leu925=) c.1920+433C= (n.1920+433C=) n.3241C= c.2353C= (p.Leu785=) c.1570C= (p.Leu524=) c.2764C= (p.Leu922=) | |
9 | g.91723721G>T | CA373793108 | ROR2 | c.2773C>A (p.Leu925Met) c.1920+433C>A (n.1920+433C>A) n.3241C>A c.2353C>A (p.Leu785Met) c.1570C>A (p.Leu524Met) c.2764C>A (p.Leu922Met) | |
9 | g.91723722C>A | CA373793110 | ROR2 | c.2772G>T (p.Glu924Asp) c.1920+432G>T (n.1920+432G>T) n.3240G>T c.2352G>T (p.Glu784Asp) c.1569G>T (p.Glu523Asp) c.2763G>T (p.Glu921Asp) | |
9 | g.91723722C>G | CA373793109 | ROR2 | c.2772G>C (p.Glu924Asp) c.1920+432G>C (n.1920+432G>C) n.3240G>C c.2352G>C (p.Glu784Asp) c.1569G>C (p.Glu523Asp) c.2763G>C (p.Glu921Asp) | |
9 | g.91723722C>T | CA465995436 | ROR2 | c.2772G>A (p.Glu924=) c.1920+432G>A (n.1920+432G>A) n.3240G>A c.2352G>A (p.Glu784=) c.1569G>A (p.Glu523=) c.2763G>A (p.Glu921=) | |
9 | g.91723723T>A | CA373793111 | ROR2 | c.2771A>T (p.Glu924Val) c.1920+431A>T (n.1920+431A>T) n.3239A>T c.2351A>T (p.Glu784Val) c.1568A>T (p.Glu523Val) c.2762A>T (p.Glu921Val) | |
9 | g.91723723T>C | CA373793113 | ROR2 | c.2771A>G (p.Glu924Gly) c.1920+431A>G (n.1920+431A>G) n.3239A>G c.2351A>G (p.Glu784Gly) c.1568A>G (p.Glu523Gly) c.2762A>G (p.Glu921Gly) | |
9 | g.91723723T>G | CA373793112 | ROR2 | c.2771A>C (p.Glu924Ala) c.1920+431A>C (n.1920+431A>C) n.3239A>C c.2351A>C (p.Glu784Ala) c.1568A>C (p.Glu523Ala) c.2762A>C (p.Glu921Ala) | |
9 | g.91723724C>A | CA373793114 | ROR2 | c.2770G>T (p.Glu924Ter) c.1920+430G>T (n.1920+430G>T) n.3238G>T c.2350G>T (p.Glu784Ter) c.1567G>T (p.Glu523Ter) c.2761G>T (p.Glu921Ter) | |
9 | g.91723724C= | CA1863921458 | ROR2 | c.2770G= (p.Glu924=) c.1920+430G= (n.1920+430G=) n.3238G= c.2350G= (p.Glu784=) c.1567G= (p.Glu523=) c.2761G= (p.Glu921=) | |
9 | g.91723724C>G | CA5120314 | ROR2 | c.2770G>C (p.Glu924Gln) c.1920+430G>C (n.1920+430G>C) n.3238G>C c.2350G>C (p.Glu784Gln) c.1567G>C (p.Glu523Gln) c.2761G>C (p.Glu921Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91723724C>T | CA373793115 | ROR2 | c.2770G>A (p.Glu924Lys) c.1920+430G>A (n.1920+430G>A) n.3238G>A c.2350G>A (p.Glu784Lys) c.1567G>A (p.Glu523Lys) c.2761G>A (p.Glu921Lys) | COSMIC |
9 | g.91723725A>C | CA465995439 | ROR2 | c.2769T>G (p.Thr923=) c.1920+429T>G (n.1920+429T>G) n.3237T>G c.2349T>G (p.Thr783=) c.1566T>G (p.Thr522=) c.2760T>G (p.Thr920=) | |
9 | g.91723725A>G | CA465995437 | ROR2 | c.2769T>C (p.Thr923=) c.1920+429T>C (n.1920+429T>C) n.3237T>C c.2349T>C (p.Thr783=) c.1566T>C (p.Thr522=) c.2760T>C (p.Thr920=) | |
9 | g.91723725A>T | CA465995438 | ROR2 | c.2769T>A (p.Thr923=) c.1920+429T>A (n.1920+429T>A) n.3237T>A c.2349T>A (p.Thr783=) c.1566T>A (p.Thr522=) c.2760T>A (p.Thr920=) | |
9 | g.91723726G>A | CA5120315 | ROR2 | c.2768C>T (p.Thr923Ile) c.1920+428C>T (n.1920+428C>T) n.3236C>T c.2348C>T (p.Thr783Ile) c.1565C>T (p.Thr522Ile) c.2759C>T (p.Thr920Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91723726G>C | CA373793116 | ROR2 | c.2768C>G (p.Thr923Ser) c.1920+428C>G (n.1920+428C>G) n.3236C>G c.2348C>G (p.Thr783Ser) c.1565C>G (p.Thr522Ser) c.2759C>G (p.Thr920Ser) | |
9 | g.91723726G= | CA1863921460 | ROR2 | c.2768C= (p.Thr923=) c.1920+428C= (n.1920+428C=) n.3236C= c.2348C= (p.Thr783=) c.1565C= (p.Thr522=) c.2759C= (p.Thr920=) | |
9 | g.91723726G>T | CA373793117 | ROR2 | c.2768C>A (p.Thr923Asn) c.1920+428C>A (n.1920+428C>A) n.3236C>A c.2348C>A (p.Thr783Asn) c.1565C>A (p.Thr522Asn) c.2759C>A (p.Thr920Asn) | |
9 | g.91723727T>A | CA373793120 | ROR2 | c.2767A>T (p.Thr923Ser) c.1920+427A>T (n.1920+427A>T) n.3235A>T c.2347A>T (p.Thr783Ser) c.1564A>T (p.Thr522Ser) c.2758A>T (p.Thr920Ser) | |
9 | g.91723727T>C | CA373793118 | ROR2 | c.2767A>G (p.Thr923Ala) c.1920+427A>G (n.1920+427A>G) n.3235A>G c.2347A>G (p.Thr783Ala) c.1564A>G (p.Thr522Ala) c.2758A>G (p.Thr920Ala) | |
9 | g.91723727T>G | CA373793119 | ROR2 | c.2767A>C (p.Thr923Pro) c.1920+427A>C (n.1920+427A>C) n.3235A>C c.2347A>C (p.Thr783Pro) c.1564A>C (p.Thr522Pro) c.2758A>C (p.Thr920Pro) | |
9 | g.91723728C>A | CA373793121 | ROR2 | c.2766G>T (p.Glu922Asp) c.1920+426G>T (n.1920+426G>T) n.3234G>T c.2346G>T (p.Glu782Asp) c.1563G>T (p.Glu521Asp) c.2757G>T (p.Glu919Asp) | COSMIC |
9 | g.91723728C= | CA1863921465 | ROR2 | c.2766G= (p.Glu922=) c.1920+426G= (n.1920+426G=) n.3234G= c.2346G= (p.Glu782=) c.1563G= (p.Glu521=) c.2757G= (p.Glu919=) | |
9 | g.91723728C>G | CA373793122 | ROR2 | c.2766G>C (p.Glu922Asp) c.1920+426G>C (n.1920+426G>C) n.3234G>C c.2346G>C (p.Glu782Asp) c.1563G>C (p.Glu521Asp) c.2757G>C (p.Glu919Asp) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723728C>T | CA465995440 | ROR2 | c.2766G>A (p.Glu922=) c.1920+426G>A (n.1920+426G>A) n.3234G>A c.2346G>A (p.Glu782=) c.1563G>A (p.Glu521=) c.2757G>A (p.Glu919=) | |
9 | g.91723729T>A | CA373793123 | ROR2 | c.2765A>T (p.Glu922Val) c.1920+425A>T (n.1920+425A>T) n.3233A>T c.2345A>T (p.Glu782Val) c.1562A>T (p.Glu521Val) c.2756A>T (p.Glu919Val) | |
9 | g.91723729T>C | CA373793124 | ROR2 | c.2765A>G (p.Glu922Gly) c.1920+425A>G (n.1920+425A>G) n.3233A>G c.2345A>G (p.Glu782Gly) c.1562A>G (p.Glu521Gly) c.2756A>G (p.Glu919Gly) | |
9 | g.91723729T>G | CA373793125 | ROR2 | c.2765A>C (p.Glu922Ala) c.1920+425A>C (n.1920+425A>C) n.3233A>C c.2345A>C (p.Glu782Ala) c.1562A>C (p.Glu521Ala) c.2756A>C (p.Glu919Ala) | |
9 | g.91723730C>A | CA373793128 | ROR2 | c.2764G>T (p.Glu922Ter) c.1920+424G>T (n.1920+424G>T) n.3232G>T c.2344G>T (p.Glu782Ter) c.1561G>T (p.Glu521Ter) c.2755G>T (p.Glu919Ter) | |
9 | g.91723730C>G | CA373793126 | ROR2 | c.2764G>C (p.Glu922Gln) c.1920+424G>C (n.1920+424G>C) n.3232G>C c.2344G>C (p.Glu782Gln) c.1561G>C (p.Glu521Gln) c.2755G>C (p.Glu919Gln) | |
9 | g.91723730C>T | CA373793127 | ROR2 | c.2764G>A (p.Glu922Lys) c.1920+424G>A (n.1920+424G>A) n.3232G>A c.2344G>A (p.Glu782Lys) c.1561G>A (p.Glu521Lys) c.2755G>A (p.Glu919Lys) | |
9 | g.91723731T>A | CA465995441 | ROR2 | c.2763A>T (p.Pro921=) c.1920+423A>T (n.1920+423A>T) n.3231A>T c.2343A>T (p.Pro781=) c.1560A>T (p.Pro520=) c.2754A>T (p.Pro918=) | |
9 | g.91723731T>C | CA465995442 | ROR2 | c.2763A>G (p.Pro921=) c.1920+423A>G (n.1920+423A>G) n.3231A>G c.2343A>G (p.Pro781=) c.1560A>G (p.Pro520=) c.2754A>G (p.Pro918=) | |
9 | g.91723731T>G | CA465995443 | ROR2 | c.2763A>C (p.Pro921=) c.1920+423A>C (n.1920+423A>C) n.3231A>C c.2343A>C (p.Pro781=) c.1560A>C (p.Pro520=) c.2754A>C (p.Pro918=) | |
9 | g.91723732G>A | CA373793129 | ROR2 | c.2762C>T (p.Pro921Leu) c.1920+422C>T (n.1920+422C>T) n.3230C>T c.2342C>T (p.Pro781Leu) c.1559C>T (p.Pro520Leu) c.2753C>T (p.Pro918Leu) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723732G>C | CA373793130 | ROR2 | c.2762C>G (p.Pro921Arg) c.1920+422C>G (n.1920+422C>G) n.3230C>G c.2342C>G (p.Pro781Arg) c.1559C>G (p.Pro520Arg) c.2753C>G (p.Pro918Arg) | |
9 | g.91723732G= | CA1863921470 | ROR2 | c.2762C= (p.Pro921=) c.1920+422C= (n.1920+422C=) n.3230C= c.2342C= (p.Pro781=) c.1559C= (p.Pro520=) c.2753C= (p.Pro918=) | |
9 | g.91723732G>T | CA373793131 | ROR2 | c.2762C>A (p.Pro921Gln) c.1920+422C>A (n.1920+422C>A) n.3230C>A c.2342C>A (p.Pro781Gln) c.1559C>A (p.Pro520Gln) c.2753C>A (p.Pro918Gln) | |
9 | g.91723733G>A | CA373793132 | ROR2 | c.2761C>T (p.Pro921Ser) c.1920+421C>T (n.1920+421C>T) n.3229C>T c.2341C>T (p.Pro781Ser) c.1558C>T (p.Pro520Ser) c.2752C>T (p.Pro918Ser) | |
9 | g.91723733G>C | CA373793133 | ROR2 | c.2761C>G (p.Pro921Ala) c.1920+421C>G (n.1920+421C>G) n.3229C>G c.2341C>G (p.Pro781Ala) c.1558C>G (p.Pro520Ala) c.2752C>G (p.Pro918Ala) | gnomAD v4 |
9 | g.91723733G= | CA1863921474 | ROR2 | c.2761C= (p.Pro921=) c.1920+421C= (n.1920+421C=) n.3229C= c.2341C= (p.Pro781=) c.1558C= (p.Pro520=) c.2752C= (p.Pro918=) | |
9 | g.91723733G>T | CA373793134 | ROR2 | c.2761C>A (p.Pro921Thr) c.1920+421C>A (n.1920+421C>A) n.3229C>A c.2341C>A (p.Pro781Thr) c.1558C>A (p.Pro520Thr) c.2752C>A (p.Pro918Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723734G>A | CA465995444 | ROR2 | c.2760C>T (p.Val920=) c.1920+420C>T (n.1920+420C>T) n.3228C>T c.2340C>T (p.Val780=) c.1557C>T (p.Val519=) c.2751C>T (p.Val917=) | dbSNP gnomAD v2 |
9 | g.91723734G>C | CA465995445 | ROR2 | c.2760C>G (p.Val920=) c.1920+420C>G (n.1920+420C>G) n.3228C>G c.2340C>G (p.Val780=) c.1557C>G (p.Val519=) c.2751C>G (p.Val917=) | gnomAD v4 |
9 | g.91723734G= | CA1863921476 | ROR2 | c.2760C= (p.Val920=) c.1920+420C= (n.1920+420C=) n.3228C= c.2340C= (p.Val780=) c.1557C= (p.Val519=) c.2751C= (p.Val917=) | |
9 | g.91723734G>T | CA465995446 | ROR2 | c.2760C>A (p.Val920=) c.1920+420C>A (n.1920+420C>A) n.3228C>A c.2340C>A (p.Val780=) c.1557C>A (p.Val519=) c.2751C>A (p.Val917=) | |
9 | g.91723735A>C | CA373793135 | ROR2 | c.2759T>G (p.Val920Gly) c.1920+419T>G (n.1920+419T>G) n.3227T>G c.2339T>G (p.Val780Gly) c.1556T>G (p.Val519Gly) c.2750T>G (p.Val917Gly) | |
9 | g.91723735A>G | CA373793136 | ROR2 | c.2759T>C (p.Val920Ala) c.1920+419T>C (n.1920+419T>C) n.3227T>C c.2339T>C (p.Val780Ala) c.1556T>C (p.Val519Ala) c.2750T>C (p.Val917Ala) | |
9 | g.91723735A>T | CA373793137 | ROR2 | c.2759T>A (p.Val920Asp) c.1920+419T>A (n.1920+419T>A) n.3227T>A c.2339T>A (p.Val780Asp) c.1556T>A (p.Val519Asp) c.2750T>A (p.Val917Asp) | |
9 | g.91723736C>A | CA373793138 | ROR2 | c.2758G>T (p.Val920Phe) c.1920+418G>T (n.1920+418G>T) n.3226G>T c.2338G>T (p.Val780Phe) c.1555G>T (p.Val519Phe) c.2749G>T (p.Val917Phe) | |
9 | g.91723736C>G | CA373793139 | ROR2 | c.2758G>C (p.Val920Leu) c.1920+418G>C (n.1920+418G>C) n.3226G>C c.2338G>C (p.Val780Leu) c.1555G>C (p.Val519Leu) c.2749G>C (p.Val917Leu) | |
9 | g.91723736C>T | CA373793140 | ROR2 | c.2758G>A (p.Val920Ile) c.1920+418G>A (n.1920+418G>A) n.3226G>A c.2338G>A (p.Val780Ile) c.1555G>A (p.Val519Ile) c.2749G>A (p.Val917Ile) | |
9 | g.91723737A= | CA1863921482 | ROR2 | c.2757T= (p.Ser919=) c.1920+417T= (n.1920+417T=) n.3225T= c.2337T= (p.Ser779=) c.1554T= (p.Ser518=) c.2748T= (p.Ser916=) | |
9 | g.91723737A>C | CA465995451 | ROR2 | c.2757T>G (p.Ser919=) c.1920+417T>G (n.1920+417T>G) n.3225T>G c.2337T>G (p.Ser779=) c.1554T>G (p.Ser518=) c.2748T>G (p.Ser916=) | |
9 | g.91723737A>G | CA5120316 | ROR2 | c.2757T>C (p.Ser919=) c.1920+417T>C (n.1920+417T>C) n.3225T>C c.2337T>C (p.Ser779=) c.1554T>C (p.Ser518=) c.2748T>C (p.Ser916=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723737A>T | CA465995453 | ROR2 | c.2757T>A (p.Ser919=) c.1920+417T>A (n.1920+417T>A) n.3225T>A c.2337T>A (p.Ser779=) c.1554T>A (p.Ser518=) c.2748T>A (p.Ser916=) | |
9 | g.91723738G>A | CA373793141 | ROR2 | c.2756C>T (p.Ser919Phe) c.1920+416C>T (n.1920+416C>T) n.3224C>T c.2336C>T (p.Ser779Phe) c.1553C>T (p.Ser518Phe) c.2747C>T (p.Ser916Phe) | gnomAD v4 COSMIC |
9 | g.91723738G>C | CA5120317 | ROR2 | c.2756C>G (p.Ser919Cys) c.1920+416C>G (n.1920+416C>G) n.3224C>G c.2336C>G (p.Ser779Cys) c.1553C>G (p.Ser518Cys) c.2747C>G (p.Ser916Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723738G= | CA1863921487 | ROR2 | c.2756C= (p.Ser919=) c.1920+416C= (n.1920+416C=) n.3224C= c.2336C= (p.Ser779=) c.1553C= (p.Ser518=) c.2747C= (p.Ser916=) | |
9 | g.91723738G>T | CA373793142 | ROR2 | c.2756C>A (p.Ser919Tyr) c.1920+416C>A (n.1920+416C>A) n.3224C>A c.2336C>A (p.Ser779Tyr) c.1553C>A (p.Ser518Tyr) c.2747C>A (p.Ser916Tyr) | |
9 | g.91723739A>C | CA373793143 | ROR2 | c.2755T>G (p.Ser919Ala) c.1920+415T>G (n.1920+415T>G) n.3223T>G c.2335T>G (p.Ser779Ala) c.1552T>G (p.Ser518Ala) c.2746T>G (p.Ser916Ala) | |
9 | g.91723739A>G | CA373793144 | ROR2 | c.2755T>C (p.Ser919Pro) c.1920+415T>C (n.1920+415T>C) n.3223T>C c.2335T>C (p.Ser779Pro) c.1552T>C (p.Ser518Pro) c.2746T>C (p.Ser916Pro) | |
9 | g.91723739A>T | CA373793145 | ROR2 | c.2755T>A (p.Ser919Thr) c.1920+415T>A (n.1920+415T>A) n.3223T>A c.2335T>A (p.Ser779Thr) c.1552T>A (p.Ser518Thr) c.2746T>A (p.Ser916Thr) | |
9 | g.91723740G>A | CA465995459 | ROR2 | c.2754C>T (p.Gly918=) c.1920+414C>T (n.1920+414C>T) n.3222C>T c.2334C>T (p.Gly778=) c.1551C>T (p.Gly517=) c.2745C>T (p.Gly915=) | |
9 | g.91723740G>C | CA465995461 | ROR2 | c.2754C>G (p.Gly918=) c.1920+414C>G (n.1920+414C>G) n.3222C>G c.2334C>G (p.Gly778=) c.1551C>G (p.Gly517=) c.2745C>G (p.Gly915=) | |
9 | g.91723740G>T | CA465995463 | ROR2 | c.2754C>A (p.Gly918=) c.1920+414C>A (n.1920+414C>A) n.3222C>A c.2334C>A (p.Gly778=) c.1551C>A (p.Gly517=) c.2745C>A (p.Gly915=) | gnomAD v4 |
9 | g.91723741C>A | CA373793146 | ROR2 | c.2753G>T (p.Gly918Val) c.1920+413G>T (n.1920+413G>T) n.3221G>T c.2333G>T (p.Gly778Val) c.1550G>T (p.Gly517Val) c.2744G>T (p.Gly915Val) | |
9 | g.91723741C>G | CA373793147 | ROR2 | c.2753G>C (p.Gly918Ala) c.1920+413G>C (n.1920+413G>C) n.3221G>C c.2333G>C (p.Gly778Ala) c.1550G>C (p.Gly517Ala) c.2744G>C (p.Gly915Ala) | |
9 | g.91723741C>T | CA373793148 | ROR2 | c.2753G>A (p.Gly918Asp) c.1920+413G>A (n.1920+413G>A) n.3221G>A c.2333G>A (p.Gly778Asp) c.1550G>A (p.Gly517Asp) c.2744G>A (p.Gly915Asp) | |
9 | g.91723742C>A | CA373793149 | ROR2 | c.2752G>T (p.Gly918Cys) c.1920+412G>T (n.1920+412G>T) n.3220G>T c.2332G>T (p.Gly778Cys) c.1549G>T (p.Gly517Cys) c.2743G>T (p.Gly915Cys) | |
9 | g.91723742C>G | CA373793150 | ROR2 | c.2752G>C (p.Gly918Arg) c.1920+412G>C (n.1920+412G>C) n.3220G>C c.2332G>C (p.Gly778Arg) c.1549G>C (p.Gly517Arg) c.2743G>C (p.Gly915Arg) | |
9 | g.91723742C>T | CA373793151 | ROR2 | c.2752G>A (p.Gly918Ser) c.1920+412G>A (n.1920+412G>A) n.3220G>A c.2332G>A (p.Gly778Ser) c.1549G>A (p.Gly517Ser) c.2743G>A (p.Gly915Ser) | |
9 | g.91723743T>A | CA373793152 | ROR2 | c.2751A>T (p.Glu917Asp) c.1920+411A>T (n.1920+411A>T) n.3219A>T c.2331A>T (p.Glu777Asp) c.1548A>T (p.Glu516Asp) c.2742A>T (p.Glu914Asp) | |
9 | g.91723743T>C | CA465995469 | ROR2 | c.2751A>G (p.Glu917=) c.1920+411A>G (n.1920+411A>G) n.3219A>G c.2331A>G (p.Glu777=) c.1548A>G (p.Glu516=) c.2742A>G (p.Glu914=) | |
9 | g.91723743T>G | CA373793153 | ROR2 | c.2751A>C (p.Glu917Asp) c.1920+411A>C (n.1920+411A>C) n.3219A>C c.2331A>C (p.Glu777Asp) c.1548A>C (p.Glu516Asp) c.2742A>C (p.Glu914Asp) | COSMIC |
9 | g.91723743_91723746delinsTTCC | CA1863921491 | ROR2 | c.2748_2751delinsGGAA (p.Glu916=) c.1920+408_1920+411delinsGGAA (n.1920+408_1920+411delinsGGAA) n.3216_3219delinsGGAA c.2328_2331delinsGGAA (p.Glu776=) c.1545_1548delinsGGAA (p.Glu515=) c.2739_2742delinsGGAA (p.Glu913=) | |
9 | g.91723744T>A | CA373793156 | ROR2 | c.2750A>T (p.Glu917Val) c.1920+410A>T (n.1920+410A>T) n.3218A>T c.2330A>T (p.Glu777Val) c.1547A>T (p.Glu516Val) c.2741A>T (p.Glu914Val) | |
9 | g.91723744T>C | CA373793154 | ROR2 | c.2750A>G (p.Glu917Gly) c.1920+410A>G (n.1920+410A>G) n.3218A>G c.2330A>G (p.Glu777Gly) c.1547A>G (p.Glu516Gly) c.2741A>G (p.Glu914Gly) | |
9 | g.91723744T>G | CA373793155 | ROR2 | c.2750A>C (p.Glu917Ala) c.1920+410A>C (n.1920+410A>C) n.3218A>C c.2330A>C (p.Glu777Ala) c.1547A>C (p.Glu516Ala) c.2741A>C (p.Glu914Ala) | |
9 | g.91723755_91723757dup | CA5120319 | ROR2 | c.2748_2750dup (p.Glu917_Gly918insGlu) c.1920+408_1920+410dup (n.1920+408_1920+410dup) n.3216_3218dup c.2328_2330dup (p.Glu777_Gly778insGlu) c.1545_1547dup (p.Glu516_Gly517insGlu) c.2739_2741dup (p.Glu914_Gly915insGlu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723755_91723757del | CA5120318 | ROR2 | c.2748_2750del (p.Glu917del) c.1920+408_1920+410del (n.1920+408_1920+410del) n.3216_3218del c.2328_2330del (p.Glu777del) c.1545_1547del (p.Glu516del) c.2739_2741del (p.Glu914del) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.91723745C>A | CA373793157 | ROR2 | c.2749G>T (p.Glu917Ter) c.1920+409G>T (n.1920+409G>T) n.3217G>T c.2329G>T (p.Glu777Ter) c.1546G>T (p.Glu516Ter) c.2740G>T (p.Glu914Ter) | |
9 | g.91723745C= | CA1863921497 | ROR2 | c.2749G= (p.Glu917=) c.1920+409G= (n.1920+409G=) n.3217G= c.2329G= (p.Glu777=) c.1546G= (p.Glu516=) c.2740G= (p.Glu914=) | |
9 | g.91723745C>G | CA5120320 | ROR2 | c.2749G>C (p.Glu917Gln) c.1920+409G>C (n.1920+409G>C) n.3217G>C c.2329G>C (p.Glu777Gln) c.1546G>C (p.Glu516Gln) c.2740G>C (p.Glu914Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91723745C>T | CA373793158 | ROR2 | c.2749G>A (p.Glu917Lys) c.1920+409G>A (n.1920+409G>A) n.3217G>A c.2329G>A (p.Glu777Lys) c.1546G>A (p.Glu516Lys) c.2740G>A (p.Glu914Lys) | |
9 | g.91723746C>A | CA373793159 | ROR2 | c.2748G>T (p.Glu916Asp) c.1920+408G>T (n.1920+408G>T) n.3216G>T c.2328G>T (p.Glu776Asp) c.1545G>T (p.Glu515Asp) c.2739G>T (p.Glu913Asp) | gnomAD v4 |
9 | g.91723746C>G | CA373793160 | ROR2 | c.2748G>C (p.Glu916Asp) c.1920+408G>C (n.1920+408G>C) n.3216G>C c.2328G>C (p.Glu776Asp) c.1545G>C (p.Glu515Asp) c.2739G>C (p.Glu913Asp) | |
9 | g.91723746C>T | CA465995482 | ROR2 | c.2748G>A (p.Glu916=) c.1920+408G>A (n.1920+408G>A) n.3216G>A c.2328G>A (p.Glu776=) c.1545G>A (p.Glu515=) c.2739G>A (p.Glu913=) | |
9 | g.91723747T>A | CA373793161 | ROR2 | c.2747A>T (p.Glu916Val) c.1920+407A>T (n.1920+407A>T) n.3215A>T c.2327A>T (p.Glu776Val) c.1544A>T (p.Glu515Val) c.2738A>T (p.Glu913Val) | |
9 | g.91723747T>C | CA373793162 | ROR2 | c.2747A>G (p.Glu916Gly) c.1920+407A>G (n.1920+407A>G) n.3215A>G c.2327A>G (p.Glu776Gly) c.1544A>G (p.Glu515Gly) c.2738A>G (p.Glu913Gly) | |
9 | g.91723747T>G | CA195321403 | ROR2 | c.2747A>C (p.Glu916Ala) c.1920+407A>C (n.1920+407A>C) n.3215A>C c.2327A>C (p.Glu776Ala) c.1544A>C (p.Glu515Ala) c.2738A>C (p.Glu913Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723747T= | CA1863921501 | ROR2 | c.2747A= (p.Glu916=) c.1920+407A= (n.1920+407A=) n.3215A= c.2327A= (p.Glu776=) c.1544A= (p.Glu515=) c.2738A= (p.Glu913=) | |
9 | g.91723748C>A | CA373793163 | ROR2 | c.2746G>T (p.Glu916Ter) c.1920+406G>T (n.1920+406G>T) n.3214G>T c.2326G>T (p.Glu776Ter) c.1543G>T (p.Glu515Ter) c.2737G>T (p.Glu913Ter) | |
9 | g.91723748C= | CA1863921508 | ROR2 | c.2746G= (p.Glu916=) c.1920+406G= (n.1920+406G=) n.3214G= c.2326G= (p.Glu776=) c.1543G= (p.Glu515=) c.2737G= (p.Glu913=) | |
9 | g.91723748C>G | CA373793164 | ROR2 | c.2746G>C (p.Glu916Gln) c.1920+406G>C (n.1920+406G>C) n.3214G>C c.2326G>C (p.Glu776Gln) c.1543G>C (p.Glu515Gln) c.2737G>C (p.Glu913Gln) | |
9 | g.91723748C>T | CA373793165 | ROR2 | c.2746G>A (p.Glu916Lys) c.1920+406G>A (n.1920+406G>A) n.3214G>A c.2326G>A (p.Glu776Lys) c.1543G>A (p.Glu515Lys) c.2737G>A (p.Glu913Lys) | dbSNP gnomAD v4 |
9 | g.91723749C>A | CA373793166 | ROR2 | c.2745G>T (p.Glu915Asp) c.1920+405G>T (n.1920+405G>T) n.3213G>T c.2325G>T (p.Glu775Asp) c.1542G>T (p.Glu514Asp) c.2736G>T (p.Glu912Asp) | |
9 | g.91723749C>G | CA373793167 | ROR2 | c.2745G>C (p.Glu915Asp) c.1920+405G>C (n.1920+405G>C) n.3213G>C c.2325G>C (p.Glu775Asp) c.1542G>C (p.Glu514Asp) c.2736G>C (p.Glu912Asp) | |
9 | g.91723749C>T | CA465995488 | ROR2 | c.2745G>A (p.Glu915=) c.1920+405G>A (n.1920+405G>A) n.3213G>A c.2325G>A (p.Glu775=) c.1542G>A (p.Glu514=) c.2736G>A (p.Glu912=) | gnomAD v4 |
9 | g.91723750T>A | CA373793168 | ROR2 | c.2744A>T (p.Glu915Val) c.1920+404A>T (n.1920+404A>T) n.3212A>T c.2324A>T (p.Glu775Val) c.1541A>T (p.Glu514Val) c.2735A>T (p.Glu912Val) | |
9 | g.91723750T>C | CA373793170 | ROR2 | c.2744A>G (p.Glu915Gly) c.1920+404A>G (n.1920+404A>G) n.3212A>G c.2324A>G (p.Glu775Gly) c.1541A>G (p.Glu514Gly) c.2735A>G (p.Glu912Gly) | |
9 | g.91723750T>G | CA373793169 | ROR2 | c.2744A>C (p.Glu915Ala) c.1920+404A>C (n.1920+404A>C) n.3212A>C c.2324A>C (p.Glu775Ala) c.1541A>C (p.Glu514Ala) c.2735A>C (p.Glu912Ala) | |
9 | g.91723751C>A | CA373793171 | ROR2 | c.2743G>T (p.Glu915Ter) c.1920+403G>T (n.1920+403G>T) n.3211G>T c.2323G>T (p.Glu775Ter) c.1540G>T (p.Glu514Ter) c.2734G>T (p.Glu912Ter) | |
9 | g.91723751C>G | CA373793172 | ROR2 | c.2743G>C (p.Glu915Gln) c.1920+403G>C (n.1920+403G>C) n.3211G>C c.2323G>C (p.Glu775Gln) c.1540G>C (p.Glu514Gln) c.2734G>C (p.Glu912Gln) | |
9 | g.91723751C>T | CA373793173 | ROR2 | c.2743G>A (p.Glu915Lys) c.1920+403G>A (n.1920+403G>A) n.3211G>A c.2323G>A (p.Glu775Lys) c.1540G>A (p.Glu514Lys) c.2734G>A (p.Glu912Lys) | |
9 | g.91723752C>A | CA373793174 | ROR2 | c.2742G>T (p.Glu914Asp) c.1920+402G>T (n.1920+402G>T) n.3210G>T c.2322G>T (p.Glu774Asp) c.1539G>T (p.Glu513Asp) c.2733G>T (p.Glu911Asp) | |
9 | g.91723752C>G | CA373793175 | ROR2 | c.2742G>C (p.Glu914Asp) c.1920+402G>C (n.1920+402G>C) n.3210G>C c.2322G>C (p.Glu774Asp) c.1539G>C (p.Glu513Asp) c.2733G>C (p.Glu911Asp) | |
9 | g.91723752C>T | CA465995492 | ROR2 | c.2742G>A (p.Glu914=) c.1920+402G>A (n.1920+402G>A) n.3210G>A c.2322G>A (p.Glu774=) c.1539G>A (p.Glu513=) c.2733G>A (p.Glu911=) | |
9 | g.91723753T>A | CA373793176 | ROR2 | c.2741A>T (p.Glu914Val) c.1920+401A>T (n.1920+401A>T) n.3209A>T c.2321A>T (p.Glu774Val) c.1538A>T (p.Glu513Val) c.2732A>T (p.Glu911Val) | |
9 | g.91723753T>C | CA373793177 | ROR2 | c.2741A>G (p.Glu914Gly) c.1920+401A>G (n.1920+401A>G) n.3209A>G c.2321A>G (p.Glu774Gly) c.1538A>G (p.Glu513Gly) c.2732A>G (p.Glu911Gly) | |
9 | g.91723753T>G | CA373793178 | ROR2 | c.2741A>C (p.Glu914Ala) c.1920+401A>C (n.1920+401A>C) n.3209A>C c.2321A>C (p.Glu774Ala) c.1538A>C (p.Glu513Ala) c.2732A>C (p.Glu911Ala) | |
9 | g.91723754C>A | CA373793179 | ROR2 | c.2740G>T (p.Glu914Ter) c.1920+400G>T (n.1920+400G>T) n.3208G>T c.2320G>T (p.Glu774Ter) c.1537G>T (p.Glu513Ter) c.2731G>T (p.Glu911Ter) | |
9 | g.91723754C= | CA1863921510 | ROR2 | c.2740G= (p.Glu914=) c.1920+400G= (n.1920+400G=) n.3208G= c.2320G= (p.Glu774=) c.1537G= (p.Glu513=) c.2731G= (p.Glu911=) | |
9 | g.91723754C>G | CA373793180 | ROR2 | c.2740G>C (p.Glu914Gln) c.1920+400G>C (n.1920+400G>C) n.3208G>C c.2320G>C (p.Glu774Gln) c.1537G>C (p.Glu513Gln) c.2731G>C (p.Glu911Gln) | |
9 | g.91723754C>T | CA373793181 | ROR2 | c.2740G>A (p.Glu914Lys) c.1920+400G>A (n.1920+400G>A) n.3208G>A c.2320G>A (p.Glu774Lys) c.1537G>A (p.Glu513Lys) c.2731G>A (p.Glu911Lys) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723755C>A | CA373793182 | ROR2 | c.2739G>T (p.Glu913Asp) c.1920+399G>T (n.1920+399G>T) n.3207G>T c.2319G>T (p.Glu773Asp) c.1536G>T (p.Glu512Asp) c.2730G>T (p.Glu910Asp) | |
9 | g.91723755C>G | CA373793183 | ROR2 | c.2739G>C (p.Glu913Asp) c.1920+399G>C (n.1920+399G>C) n.3207G>C c.2319G>C (p.Glu773Asp) c.1536G>C (p.Glu512Asp) c.2730G>C (p.Glu910Asp) | |
9 | g.91723755C>T | CA465995500 | ROR2 | c.2739G>A (p.Glu913=) c.1920+399G>A (n.1920+399G>A) n.3207G>A c.2319G>A (p.Glu773=) c.1536G>A (p.Glu512=) c.2730G>A (p.Glu910=) | |
9 | g.91723755_91723758delinsCTCT | CA1863921513 | ROR2 | c.2736_2739delinsAGAG (p.Ala912=) c.1920+396_1920+399delinsAGAG (n.1920+396_1920+399delinsAGAG) n.3204_3207delinsAGAG c.2316_2319delinsAGAG (p.Ala772=) c.1533_1536delinsAGAG (p.Ala511=) c.2727_2730delinsAGAG (p.Ala909=) | |
9 | g.91723756T>A | CA373793184 | ROR2 | c.2738A>T (p.Glu913Val) c.1920+398A>T (n.1920+398A>T) n.3206A>T c.2318A>T (p.Glu773Val) c.1535A>T (p.Glu512Val) c.2729A>T (p.Glu910Val) | |
9 | g.91723756T>C | CA373793186 | ROR2 | c.2738A>G (p.Glu913Gly) c.1920+398A>G (n.1920+398A>G) n.3206A>G c.2318A>G (p.Glu773Gly) c.1535A>G (p.Glu512Gly) c.2729A>G (p.Glu910Gly) | gnomAD v4 |
9 | g.91723756T>G | CA373793185 | ROR2 | c.2738A>C (p.Glu913Ala) c.1920+398A>C (n.1920+398A>C) n.3206A>C c.2318A>C (p.Glu773Ala) c.1535A>C (p.Glu512Ala) c.2729A>C (p.Glu910Ala) | dbSNP gnomAD v2 |
9 | g.91723756T= | CA1863921516 | ROR2 | c.2738A= (p.Glu913=) c.1920+398A= (n.1920+398A=) n.3206A= c.2318A= (p.Glu773=) c.1535A= (p.Glu512=) c.2729A= (p.Glu910=) | |
9 | g.91723756_91723758del | CA5120321 | ROR2 | c.2736_2738del (p.Glu913del) c.1920+396_1920+398del (n.1920+396_1920+398del) n.3204_3206del c.2316_2318del (p.Glu773del) c.1533_1535del (p.Glu512del) c.2727_2729del (p.Glu910del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723757C>A | CA373793187 | ROR2 | c.2737G>T (p.Glu913Ter) c.1920+397G>T (n.1920+397G>T) n.3205G>T c.2317G>T (p.Glu773Ter) c.1534G>T (p.Glu512Ter) c.2728G>T (p.Glu910Ter) | |
9 | g.91723757C= | CA1863921520 | ROR2 | c.2737G= (p.Glu913=) c.1920+397G= (n.1920+397G=) n.3205G= c.2317G= (p.Glu773=) c.1534G= (p.Glu512=) c.2728G= (p.Glu910=) | |
9 | g.91723757C>G | CA373793188 | ROR2 | c.2737G>C (p.Glu913Gln) c.1920+397G>C (n.1920+397G>C) n.3205G>C c.2317G>C (p.Glu773Gln) c.1534G>C (p.Glu512Gln) c.2728G>C (p.Glu910Gln) | dbSNP |
9 | g.91723757C>T | CA373793189 | ROR2 | c.2737G>A (p.Glu913Lys) c.1920+397G>A (n.1920+397G>A) n.3205G>A c.2317G>A (p.Glu773Lys) c.1534G>A (p.Glu512Lys) c.2728G>A (p.Glu910Lys) | |
9 | g.91723758T>A | CA465995507 | ROR2 | c.2736A>T (p.Ala912=) c.1920+396A>T (n.1920+396A>T) n.3204A>T c.2316A>T (p.Ala772=) c.1533A>T (p.Ala511=) c.2727A>T (p.Ala909=) | |
9 | g.91723758T>C | CA465995508 | ROR2 | c.2736A>G (p.Ala912=) c.1920+396A>G (n.1920+396A>G) n.3204A>G c.2316A>G (p.Ala772=) c.1533A>G (p.Ala511=) c.2727A>G (p.Ala909=) | |
9 | g.91723758T>G | CA465995510 | ROR2 | c.2736A>C (p.Ala912=) c.1920+396A>C (n.1920+396A>C) n.3204A>C c.2316A>C (p.Ala772=) c.1533A>C (p.Ala511=) c.2727A>C (p.Ala909=) | |
9 | g.91723759G>A | CA373793190 | ROR2 | c.2735C>T (p.Ala912Val) c.1920+395C>T (n.1920+395C>T) n.3203C>T c.2315C>T (p.Ala772Val) c.1532C>T (p.Ala511Val) c.2726C>T (p.Ala909Val) | |
9 | g.91723759G>C | CA373793191 | ROR2 | c.2735C>G (p.Ala912Gly) c.1920+395C>G (n.1920+395C>G) n.3203C>G c.2315C>G (p.Ala772Gly) c.1532C>G (p.Ala511Gly) c.2726C>G (p.Ala909Gly) | |
9 | g.91723759G>T | CA373793192 | ROR2 | c.2735C>A (p.Ala912Glu) c.1920+395C>A (n.1920+395C>A) n.3203C>A c.2315C>A (p.Ala772Glu) c.1532C>A (p.Ala511Glu) c.2726C>A (p.Ala909Glu) | gnomAD v4 |
9 | g.91723760C>A | CA373793193 | ROR2 | c.2734G>T (p.Ala912Ser) c.1920+394G>T (n.1920+394G>T) n.3202G>T c.2314G>T (p.Ala772Ser) c.1531G>T (p.Ala511Ser) c.2725G>T (p.Ala909Ser) | |
9 | g.91723760C= | CA1863921522 | ROR2 | c.2734G= (p.Ala912=) c.1920+394G= (n.1920+394G=) n.3202G= c.2314G= (p.Ala772=) c.1531G= (p.Ala511=) c.2725G= (p.Ala909=) | |
9 | g.91723760C>G | CA373793194 | ROR2 | c.2734G>C (p.Ala912Pro) c.1920+394G>C (n.1920+394G>C) n.3202G>C c.2314G>C (p.Ala772Pro) c.1531G>C (p.Ala511Pro) c.2725G>C (p.Ala909Pro) | |
9 | g.91723760C>T | CA373793195 | ROR2 | c.2734G>A (p.Ala912Thr) c.1920+394G>A (n.1920+394G>A) n.3202G>A c.2314G>A (p.Ala772Thr) c.1531G>A (p.Ala511Thr) c.2725G>A (p.Ala909Thr) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723761T>A | CA373793197 | ROR2 | c.2733A>T (p.Glu911Asp) c.1920+393A>T (n.1920+393A>T) n.3201A>T c.2313A>T (p.Glu771Asp) c.1530A>T (p.Glu510Asp) c.2724A>T (p.Glu908Asp) | |
9 | g.91723761T>C | CA466334432 | ROR2 | c.2733A>G (p.Glu911=) c.1920+393A>G (n.1920+393A>G) n.3201A>G c.2313A>G (p.Glu771=) c.1530A>G (p.Glu510=) c.2724A>G (p.Glu908=) | |
9 | g.91723761T>G | CA373793196 | ROR2 | c.2733A>C (p.Glu911Asp) c.1920+393A>C (n.1920+393A>C) n.3201A>C c.2313A>C (p.Glu771Asp) c.1530A>C (p.Glu510Asp) c.2724A>C (p.Glu908Asp) | |
9 | g.91723762T>A | CA373793198 | ROR2 | c.2732A>T (p.Glu911Val) c.1920+392A>T (n.1920+392A>T) n.3200A>T c.2312A>T (p.Glu771Val) c.1529A>T (p.Glu510Val) c.2723A>T (p.Glu908Val) | |
9 | g.91723762T>C | CA373793199 | ROR2 | c.2732A>G (p.Glu911Gly) c.1920+392A>G (n.1920+392A>G) n.3200A>G c.2312A>G (p.Glu771Gly) c.1529A>G (p.Glu510Gly) c.2723A>G (p.Glu908Gly) | gnomAD v4 |
9 | g.91723762T>G | CA373793200 | ROR2 | c.2732A>C (p.Glu911Ala) c.1920+392A>C (n.1920+392A>C) n.3200A>C c.2312A>C (p.Glu771Ala) c.1529A>C (p.Glu510Ala) c.2723A>C (p.Glu908Ala) | |
9 | g.91723763C>A | CA373793201 | ROR2 | c.2731G>T (p.Glu911Ter) c.1920+391G>T (n.1920+391G>T) n.3199G>T c.2311G>T (p.Glu771Ter) c.1528G>T (p.Glu510Ter) c.2722G>T (p.Glu908Ter) | gnomAD v4 |
9 | g.91723763C= | CA1863921527 | ROR2 | c.2731G= (p.Glu911=) c.1920+391G= (n.1920+391G=) n.3199G= c.2311G= (p.Glu771=) c.1528G= (p.Glu510=) c.2722G= (p.Glu908=) | |
9 | g.91723763C>G | CA373793202 | ROR2 | c.2731G>C (p.Glu911Gln) c.1920+391G>C (n.1920+391G>C) n.3199G>C c.2311G>C (p.Glu771Gln) c.1528G>C (p.Glu510Gln) c.2722G>C (p.Glu908Gln) | |
9 | g.91723763C>T | CA373793203 | ROR2 | c.2731G>A (p.Glu911Lys) c.1920+391G>A (n.1920+391G>A) n.3199G>A c.2311G>A (p.Glu771Lys) c.1528G>A (p.Glu510Lys) c.2722G>A (p.Glu908Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723764C>A | CA373793204 | ROR2 | c.2730G>T (p.Gln910His) c.1920+390G>T (n.1920+390G>T) n.3198G>T c.2310G>T (p.Gln770His) c.1527G>T (p.Gln509His) c.2721G>T (p.Gln907His) | |
9 | g.91723764C>G | CA373793205 | ROR2 | c.2730G>C (p.Gln910His) c.1920+390G>C (n.1920+390G>C) n.3198G>C c.2310G>C (p.Gln770His) c.1527G>C (p.Gln509His) c.2721G>C (p.Gln907His) | |
9 | g.91723764C>T | CA466334433 | ROR2 | c.2730G>A (p.Gln910=) c.1920+390G>A (n.1920+390G>A) n.3198G>A c.2310G>A (p.Gln770=) c.1527G>A (p.Gln509=) c.2721G>A (p.Gln907=) | |
9 | g.91723765T>A | CA373793206 | ROR2 | c.2729A>T (p.Gln910Leu) c.1920+389A>T (n.1920+389A>T) n.3197A>T c.2309A>T (p.Gln770Leu) c.1526A>T (p.Gln509Leu) c.2720A>T (p.Gln907Leu) | |
9 | g.91723765T>C | CA373793208 | ROR2 | c.2729A>G (p.Gln910Arg) c.1920+389A>G (n.1920+389A>G) n.3197A>G c.2309A>G (p.Gln770Arg) c.1526A>G (p.Gln509Arg) c.2720A>G (p.Gln907Arg) | ClinVar gnomAD v4 |
9 | g.91723765T>G | CA373793207 | ROR2 | c.2729A>C (p.Gln910Pro) c.1920+389A>C (n.1920+389A>C) n.3197A>C c.2309A>C (p.Gln770Pro) c.1526A>C (p.Gln509Pro) c.2720A>C (p.Gln907Pro) | |
9 | g.91723766G>A | CA373793209 | ROR2 | c.2728C>T (p.Gln910Ter) c.1920+388C>T (n.1920+388C>T) n.3196C>T c.2308C>T (p.Gln770Ter) c.1525C>T (p.Gln509Ter) c.2719C>T (p.Gln907Ter) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723766G>C | CA373793210 | ROR2 | c.2728C>G (p.Gln910Glu) c.1920+388C>G (n.1920+388C>G) n.3196C>G c.2308C>G (p.Gln770Glu) c.1525C>G (p.Gln509Glu) c.2719C>G (p.Gln907Glu) | |
9 | g.91723766G= | CA1863921530 | ROR2 | c.2728C= (p.Gln910=) c.1920+388C= (n.1920+388C=) n.3196C= c.2308C= (p.Gln770=) c.1525C= (p.Gln509=) c.2719C= (p.Gln907=) | |
9 | g.91723766G>T | CA373793211 | ROR2 | c.2728C>A (p.Gln910Lys) c.1920+388C>A (n.1920+388C>A) n.3196C>A c.2308C>A (p.Gln770Lys) c.1525C>A (p.Gln509Lys) c.2719C>A (p.Gln907Lys) | |
9 | g.91723767C>A | CA466334434 | ROR2 | c.2727G>T (p.Val909=) c.1920+387G>T (n.1920+387G>T) n.3195G>T c.2307G>T (p.Val769=) c.1524G>T (p.Val508=) c.2718G>T (p.Val906=) | dbSNP gnomAD v2 |
9 | g.91723767C= | CA1863921535 | ROR2 | c.2727G= (p.Val909=) c.1920+387G= (n.1920+387G=) n.3195G= c.2307G= (p.Val769=) c.1524G= (p.Val508=) c.2718G= (p.Val906=) | |
9 | g.91723767C>G | CA466334435 | ROR2 | c.2727G>C (p.Val909=) c.1920+387G>C (n.1920+387G>C) n.3195G>C c.2307G>C (p.Val769=) c.1524G>C (p.Val508=) c.2718G>C (p.Val906=) | |
9 | g.91723767C>T | CA5120322 | ROR2 | c.2727G>A (p.Val909=) c.1920+387G>A (n.1920+387G>A) n.3195G>A c.2307G>A (p.Val769=) c.1524G>A (p.Val508=) c.2718G>A (p.Val906=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723768A= | CA1863921539 | ROR2 | c.2726T= (p.Val909=) c.1920+386T= (n.1920+386T=) n.3194T= c.2306T= (p.Val769=) c.1523T= (p.Val508=) c.2717T= (p.Val906=) | |
9 | g.91723768A>C | CA373793212 | ROR2 | c.2726T>G (p.Val909Gly) c.1920+386T>G (n.1920+386T>G) n.3194T>G c.2306T>G (p.Val769Gly) c.1523T>G (p.Val508Gly) c.2717T>G (p.Val906Gly) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91723768A>G | CA373793214 | ROR2 | c.2726T>C (p.Val909Ala) c.1920+386T>C (n.1920+386T>C) n.3194T>C c.2306T>C (p.Val769Ala) c.1523T>C (p.Val508Ala) c.2717T>C (p.Val906Ala) | |
9 | g.91723768A>T | CA373793213 | ROR2 | c.2726T>A (p.Val909Glu) c.1920+386T>A (n.1920+386T>A) n.3194T>A c.2306T>A (p.Val769Glu) c.1523T>A (p.Val508Glu) c.2717T>A (p.Val906Glu) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723769C>A | CA373793215 | ROR2 | c.2725G>T (p.Val909Leu) c.1920+385G>T (n.1920+385G>T) n.3193G>T c.2305G>T (p.Val769Leu) c.1522G>T (p.Val508Leu) c.2716G>T (p.Val906Leu) | |
9 | g.91723769C= | CA1863921545 | ROR2 | c.2725G= (p.Val909=) c.1920+385G= (n.1920+385G=) n.3193G= c.2305G= (p.Val769=) c.1522G= (p.Val508=) c.2716G= (p.Val906=) | |
9 | g.91723769C>G | CA373793216 | ROR2 | c.2725G>C (p.Val909Leu) c.1920+385G>C (n.1920+385G>C) n.3193G>C c.2305G>C (p.Val769Leu) c.1522G>C (p.Val508Leu) c.2716G>C (p.Val906Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723769C>T | CA5120323 | ROR2 | c.2725G>A (p.Val909Met) c.1920+385G>A (n.1920+385G>A) n.3193G>A c.2305G>A (p.Val769Met) c.1522G>A (p.Val508Met) c.2716G>A (p.Val906Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.91723770G>A | CA5120324 | ROR2 | c.2724C>T (p.Thr908=) c.1920+384C>T (n.1920+384C>T) n.3192C>T c.2304C>T (p.Thr768=) c.1521C>T (p.Thr507=) c.2715C>T (p.Thr905=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723770G>C | CA466334436 | ROR2 | c.2724C>G (p.Thr908=) c.1920+384C>G (n.1920+384C>G) n.3192C>G c.2304C>G (p.Thr768=) c.1521C>G (p.Thr507=) c.2715C>G (p.Thr905=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723770G= | CA1863921552 | ROR2 | c.2724C= (p.Thr908=) c.1920+384C= (n.1920+384C=) n.3192C= c.2304C= (p.Thr768=) c.1521C= (p.Thr507=) c.2715C= (p.Thr905=) | |
9 | g.91723770G>T | CA466334437 | ROR2 | c.2724C>A (p.Thr908=) c.1920+384C>A (n.1920+384C>A) n.3192C>A c.2304C>A (p.Thr768=) c.1521C>A (p.Thr507=) c.2715C>A (p.Thr905=) | COSMIC |
9 | g.91723771G>A | CA373793217 | ROR2 | c.2723C>T (p.Thr908Ile) c.1920+383C>T (n.1920+383C>T) n.3191C>T c.2303C>T (p.Thr768Ile) c.1520C>T (p.Thr507Ile) c.2714C>T (p.Thr905Ile) | gnomAD v4 |
9 | g.91723771G>C | CA373793218 | ROR2 | c.2723C>G (p.Thr908Ser) c.1920+383C>G (n.1920+383C>G) n.3191C>G c.2303C>G (p.Thr768Ser) c.1520C>G (p.Thr507Ser) c.2714C>G (p.Thr905Ser) | |
9 | g.91723771G>T | CA373793219 | ROR2 | c.2723C>A (p.Thr908Asn) c.1920+383C>A (n.1920+383C>A) n.3191C>A c.2303C>A (p.Thr768Asn) c.1520C>A (p.Thr507Asn) c.2714C>A (p.Thr905Asn) | |
9 | g.91723772T>A | CA373793220 | ROR2 | c.2722A>T (p.Thr908Ser) c.1920+382A>T (n.1920+382A>T) n.3190A>T c.2302A>T (p.Thr768Ser) c.1519A>T (p.Thr507Ser) c.2713A>T (p.Thr905Ser) | |
9 | g.91723772T>C | CA373793221 | ROR2 | c.2722A>G (p.Thr908Ala) c.1920+382A>G (n.1920+382A>G) n.3190A>G c.2302A>G (p.Thr768Ala) c.1519A>G (p.Thr507Ala) c.2713A>G (p.Thr905Ala) | |
9 | g.91723772T>G | CA373793222 | ROR2 | c.2722A>C (p.Thr908Pro) c.1920+382A>C (n.1920+382A>C) n.3190A>C c.2302A>C (p.Thr768Pro) c.1519A>C (p.Thr507Pro) c.2713A>C (p.Thr905Pro) | dbSNP |
9 | g.91723773G>A | CA195321461 | ROR2 | c.2721C>T (p.Ser907=) c.1920+381C>T (n.1920+381C>T) n.3189C>T c.2301C>T (p.Ser767=) c.1518C>T (p.Ser506=) c.2712C>T (p.Ser904=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723773G>C | CA373793223 | ROR2 | c.2721C>G (p.Ser907Arg) c.1920+381C>G (n.1920+381C>G) n.3189C>G c.2301C>G (p.Ser767Arg) c.1518C>G (p.Ser506Arg) c.2712C>G (p.Ser904Arg) | |
9 | g.91723773G= | CA1863921555 | ROR2 | c.2721C= (p.Ser907=) c.1920+381C= (n.1920+381C=) n.3189C= c.2301C= (p.Ser767=) c.1518C= (p.Ser506=) c.2712C= (p.Ser904=) | |
9 | g.91723773G>T | CA373793224 | ROR2 | c.2721C>A (p.Ser907Arg) c.1920+381C>A (n.1920+381C>A) n.3189C>A c.2301C>A (p.Ser767Arg) c.1518C>A (p.Ser506Arg) c.2712C>A (p.Ser904Arg) | |
9 | g.91723774C>A | CA373793227 | ROR2 | c.2720G>T (p.Ser907Ile) c.1920+380G>T (n.1920+380G>T) n.3188G>T c.2300G>T (p.Ser767Ile) c.1517G>T (p.Ser506Ile) c.2711G>T (p.Ser904Ile) | |
9 | g.91723774C>G | CA373793226 | ROR2 | c.2720G>C (p.Ser907Thr) c.1920+380G>C (n.1920+380G>C) n.3188G>C c.2300G>C (p.Ser767Thr) c.1517G>C (p.Ser506Thr) c.2711G>C (p.Ser904Thr) | |
9 | g.91723774C>T | CA373793225 | ROR2 | c.2720G>A (p.Ser907Asn) c.1920+380G>A (n.1920+380G>A) n.3188G>A c.2300G>A (p.Ser767Asn) c.1517G>A (p.Ser506Asn) c.2711G>A (p.Ser904Asn) | |
9 | g.91723775T>A | CA373793229 | ROR2 | c.2719A>T (p.Ser907Cys) c.1920+379A>T (n.1920+379A>T) n.3187A>T c.2299A>T (p.Ser767Cys) c.1516A>T (p.Ser506Cys) c.2710A>T (p.Ser904Cys) | |
9 | g.91723775T>C | CA373793228 | ROR2 | c.2719A>G (p.Ser907Gly) c.1920+379A>G (n.1920+379A>G) n.3187A>G c.2299A>G (p.Ser767Gly) c.1516A>G (p.Ser506Gly) c.2710A>G (p.Ser904Gly) | gnomAD v4 |
9 | g.91723775T>G | CA373793230 | ROR2 | c.2719A>C (p.Ser907Arg) c.1920+379A>C (n.1920+379A>C) n.3187A>C c.2299A>C (p.Ser767Arg) c.1516A>C (p.Ser506Arg) c.2710A>C (p.Ser904Arg) | |
9 | g.91723776C>A | CA373793231 | ROR2 | c.2718G>T (p.Gln906His) c.1920+378G>T (n.1920+378G>T) n.3186G>T c.2298G>T (p.Gln766His) c.1515G>T (p.Gln505His) c.2709G>T (p.Gln903His) | |
9 | g.91723776C>G | CA373793232 | ROR2 | c.2718G>C (p.Gln906His) c.1920+378G>C (n.1920+378G>C) n.3186G>C c.2298G>C (p.Gln766His) c.1515G>C (p.Gln505His) c.2709G>C (p.Gln903His) | |
9 | g.91723776C>T | CA466334438 | ROR2 | c.2718G>A (p.Gln906=) c.1920+378G>A (n.1920+378G>A) n.3186G>A c.2298G>A (p.Gln766=) c.1515G>A (p.Gln505=) c.2709G>A (p.Gln903=) | |
9 | g.91723777T>A | CA373793233 | ROR2 | c.2717A>T (p.Gln906Leu) c.1920+377A>T (n.1920+377A>T) n.3185A>T c.2297A>T (p.Gln766Leu) c.1514A>T (p.Gln505Leu) c.2708A>T (p.Gln903Leu) | |
9 | g.91723777T>C | CA5120325 | ROR2 | c.2717A>G (p.Gln906Arg) c.1920+377A>G (n.1920+377A>G) n.3185A>G c.2297A>G (p.Gln766Arg) c.1514A>G (p.Gln505Arg) c.2708A>G (p.Gln903Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91723777T>G | CA373793234 | ROR2 | c.2717A>C (p.Gln906Pro) c.1920+377A>C (n.1920+377A>C) n.3185A>C c.2297A>C (p.Gln766Pro) c.1514A>C (p.Gln505Pro) c.2708A>C (p.Gln903Pro) | |
9 | g.91723777T= | CA1863921563 | ROR2 | c.2717A= (p.Gln906=) c.1920+377A= (n.1920+377A=) n.3185A= c.2297A= (p.Gln766=) c.1514A= (p.Gln505=) c.2708A= (p.Gln903=) | |
9 | g.91723778G>A | CA373793237 | ROR2 | c.2716C>T (p.Gln906Ter) c.1920+376C>T (n.1920+376C>T) n.3184C>T c.2296C>T (p.Gln766Ter) c.1513C>T (p.Gln505Ter) c.2707C>T (p.Gln903Ter) | gnomAD v4 |
9 | g.91723778G>C | CA373793236 | ROR2 | c.2716C>G (p.Gln906Glu) c.1920+376C>G (n.1920+376C>G) n.3184C>G c.2296C>G (p.Gln766Glu) c.1513C>G (p.Gln505Glu) c.2707C>G (p.Gln903Glu) | |
9 | g.91723778G>T | CA373793235 | ROR2 | c.2716C>A (p.Gln906Lys) c.1920+376C>A (n.1920+376C>A) n.3184C>A c.2296C>A (p.Gln766Lys) c.1513C>A (p.Gln505Lys) c.2707C>A (p.Gln903Lys) | gnomAD v4 |
9 | g.91723779G>A | CA466334439 | ROR2 | c.2715C>T (p.Ala905=) c.1920+375C>T (n.1920+375C>T) n.3183C>T c.2295C>T (p.Ala765=) c.1512C>T (p.Ala504=) c.2706C>T (p.Ala902=) | gnomAD v4 |
9 | g.91723779G>C | CA466334440 | ROR2 | c.2715C>G (p.Ala905=) c.1920+375C>G (n.1920+375C>G) n.3183C>G c.2295C>G (p.Ala765=) c.1512C>G (p.Ala504=) c.2706C>G (p.Ala902=) | |
9 | g.91723779G>T | CA466334441 | ROR2 | c.2715C>A (p.Ala905=) c.1920+375C>A (n.1920+375C>A) n.3183C>A c.2295C>A (p.Ala765=) c.1512C>A (p.Ala504=) c.2706C>A (p.Ala902=) | |
9 | g.91723780G>A | CA373793238 | ROR2 | c.2714C>T (p.Ala905Val) c.1920+374C>T (n.1920+374C>T) n.3182C>T c.2294C>T (p.Ala765Val) c.1511C>T (p.Ala504Val) c.2705C>T (p.Ala902Val) | gnomAD v4 |
9 | g.91723780G>C | CA373793239 | ROR2 | c.2714C>G (p.Ala905Gly) c.1920+374C>G (n.1920+374C>G) n.3182C>G c.2294C>G (p.Ala765Gly) c.1511C>G (p.Ala504Gly) c.2705C>G (p.Ala902Gly) | |
9 | g.91723780G>T | CA373793240 | ROR2 | c.2714C>A (p.Ala905Asp) c.1920+374C>A (n.1920+374C>A) n.3182C>A c.2294C>A (p.Ala765Asp) c.1511C>A (p.Ala504Asp) c.2705C>A (p.Ala902Asp) | gnomAD v4 |
9 | g.91723781C>A | CA373793241 | ROR2 | c.2713G>T (p.Ala905Ser) c.1920+373G>T (n.1920+373G>T) n.3181G>T c.2293G>T (p.Ala765Ser) c.1510G>T (p.Ala504Ser) c.2704G>T (p.Ala902Ser) | |
9 | g.91723781C= | CA1863921566 | ROR2 | c.2713G= (p.Ala905=) c.1920+373G= (n.1920+373G=) n.3181G= c.2293G= (p.Ala765=) c.1510G= (p.Ala504=) c.2704G= (p.Ala902=) | |
9 | g.91723781C>G | CA5120326 | ROR2 | c.2713G>C (p.Ala905Pro) c.1920+373G>C (n.1920+373G>C) n.3181G>C c.2293G>C (p.Ala765Pro) c.1510G>C (p.Ala504Pro) c.2704G>C (p.Ala902Pro) | ClinVar dbSNP ExAC gnomAD v2 |
9 | g.91723781C>T | CA373793242 | ROR2 | c.2713G>A (p.Ala905Thr) c.1920+373G>A (n.1920+373G>A) n.3181G>A c.2293G>A (p.Ala765Thr) c.1510G>A (p.Ala504Thr) c.2704G>A (p.Ala902Thr) | |
9 | g.91723782C>A | CA466334442 | ROR2 | c.2712G>T (p.Gly904=) c.1920+372G>T (n.1920+372G>T) n.3180G>T c.2292G>T (p.Gly764=) c.1509G>T (p.Gly503=) c.2703G>T (p.Gly901=) | |
9 | g.91723782C>G | CA466334444 | ROR2 | c.2712G>C (p.Gly904=) c.1920+372G>C (n.1920+372G>C) n.3180G>C c.2292G>C (p.Gly764=) c.1509G>C (p.Gly503=) c.2703G>C (p.Gly901=) | |
9 | g.91723782C>T | CA466334443 | ROR2 | c.2712G>A (p.Gly904=) c.1920+372G>A (n.1920+372G>A) n.3180G>A c.2292G>A (p.Gly764=) c.1509G>A (p.Gly503=) c.2703G>A (p.Gly901=) | |
9 | g.91723783C>A | CA373793244 | ROR2 | c.2711G>T (p.Gly904Val) c.1920+371G>T (n.1920+371G>T) n.3179G>T c.2291G>T (p.Gly764Val) c.1508G>T (p.Gly503Val) c.2702G>T (p.Gly901Val) | |
9 | g.91723783C= | CA1863921572 | ROR2 | c.2711G= (p.Gly904=) c.1920+371G= (n.1920+371G=) n.3179G= c.2291G= (p.Gly764=) c.1508G= (p.Gly503=) c.2702G= (p.Gly901=) | |
9 | g.91723783C>G | CA373793243 | ROR2 | c.2711G>C (p.Gly904Ala) c.1920+371G>C (n.1920+371G>C) n.3179G>C c.2291G>C (p.Gly764Ala) c.1508G>C (p.Gly503Ala) c.2702G>C (p.Gly901Ala) | |
9 | g.91723783C>T | CA5120327 | ROR2 | c.2711G>A (p.Gly904Glu) c.1920+371G>A (n.1920+371G>A) n.3179G>A c.2291G>A (p.Gly764Glu) c.1508G>A (p.Gly503Glu) c.2702G>A (p.Gly901Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91723784C>A | CA373793245 | ROR2 | c.2710G>T (p.Gly904Trp) c.1920+370G>T (n.1920+370G>T) n.3178G>T c.2290G>T (p.Gly764Trp) c.1507G>T (p.Gly503Trp) c.2701G>T (p.Gly901Trp) | COSMIC |
9 | g.91723784C>G | CA373793246 | ROR2 | c.2710G>C (p.Gly904Arg) c.1920+370G>C (n.1920+370G>C) n.3178G>C c.2290G>C (p.Gly764Arg) c.1507G>C (p.Gly503Arg) c.2701G>C (p.Gly901Arg) | |
9 | g.91723784C>T | CA373793247 | ROR2 | c.2710G>A (p.Gly904Arg) c.1920+370G>A (n.1920+370G>A) n.3178G>A c.2290G>A (p.Gly764Arg) c.1507G>A (p.Gly503Arg) c.2701G>A (p.Gly901Arg) | |
9 | g.91723785A= | CA1863921575 | ROR2 | c.2709T= (p.Asp903=) c.1920+369T= (n.1920+369T=) n.3177T= c.2289T= (p.Asp763=) c.1506T= (p.Asp502=) c.2700T= (p.Asp900=) | |
9 | g.91723785A>C | CA373793248 | ROR2 | c.2709T>G (p.Asp903Glu) c.1920+369T>G (n.1920+369T>G) n.3177T>G c.2289T>G (p.Asp763Glu) c.1506T>G (p.Asp502Glu) c.2700T>G (p.Asp900Glu) | |
9 | g.91723785A>G | CA466334445 | ROR2 | c.2709T>C (p.Asp903=) c.1920+369T>C (n.1920+369T>C) n.3177T>C c.2289T>C (p.Asp763=) c.1506T>C (p.Asp502=) c.2700T>C (p.Asp900=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723785A>T | CA373793249 | ROR2 | c.2709T>A (p.Asp903Glu) c.1920+369T>A (n.1920+369T>A) n.3177T>A c.2289T>A (p.Asp763Glu) c.1506T>A (p.Asp502Glu) c.2700T>A (p.Asp900Glu) | |
9 | g.91723786T>A | CA373793250 | ROR2 | c.2708A>T (p.Asp903Val) c.1920+368A>T (n.1920+368A>T) n.3176A>T c.2288A>T (p.Asp763Val) c.1505A>T (p.Asp502Val) c.2699A>T (p.Asp900Val) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91723786T>C | CA373793251 | ROR2 | c.2708A>G (p.Asp903Gly) c.1920+368A>G (n.1920+368A>G) n.3176A>G c.2288A>G (p.Asp763Gly) c.1505A>G (p.Asp502Gly) c.2699A>G (p.Asp900Gly) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91723786T>G | CA373793252 | ROR2 | c.2708A>C (p.Asp903Ala) c.1920+368A>C (n.1920+368A>C) n.3176A>C c.2288A>C (p.Asp763Ala) c.1505A>C (p.Asp502Ala) c.2699A>C (p.Asp900Ala) | |
9 | g.91723786T= | CA1863921581 | ROR2 | c.2708A= (p.Asp903=) c.1920+368A= (n.1920+368A=) n.3176A= c.2288A= (p.Asp763=) c.1505A= (p.Asp502=) c.2699A= (p.Asp900=) | |
9 | g.91723787C>A | CA373793253 | ROR2 | c.2707G>T (p.Asp903Tyr) c.1920+367G>T (n.1920+367G>T) n.3175G>T c.2287G>T (p.Asp763Tyr) c.1504G>T (p.Asp502Tyr) c.2698G>T (p.Asp900Tyr) | |
9 | g.91723787C= | CA1863921584 | ROR2 | c.2707G= (p.Asp903=) c.1920+367G= (n.1920+367G=) n.3175G= c.2287G= (p.Asp763=) c.1504G= (p.Asp502=) c.2698G= (p.Asp900=) | |
9 | g.91723787C>G | CA373793254 | ROR2 | c.2707G>C (p.Asp903His) c.1920+367G>C (n.1920+367G>C) n.3175G>C c.2287G>C (p.Asp763His) c.1504G>C (p.Asp502His) c.2698G>C (p.Asp900His) | |
9 | g.91723787C>T | CA373793255 | ROR2 | c.2707G>A (p.Asp903Asn) c.1920+367G>A (n.1920+367G>A) n.3175G>A c.2287G>A (p.Asp763Asn) c.1504G>A (p.Asp502Asn) c.2698G>A (p.Asp900Asn) | dbSNP |
9 | g.91723788T>A | CA373793256 | ROR2 | c.2706A>T (p.Glu902Asp) c.1920+366A>T (n.1920+366A>T) n.3174A>T c.2286A>T (p.Glu762Asp) c.1503A>T (p.Glu501Asp) c.2697A>T (p.Glu899Asp) | |
9 | g.91723788T>C | CA466334446 | ROR2 | c.2706A>G (p.Glu902=) c.1920+366A>G (n.1920+366A>G) n.3174A>G c.2286A>G (p.Glu762=) c.1503A>G (p.Glu501=) c.2697A>G (p.Glu899=) | |
9 | g.91723788T>G | CA373793257 | ROR2 | c.2706A>C (p.Glu902Asp) c.1920+366A>C (n.1920+366A>C) n.3174A>C c.2286A>C (p.Glu762Asp) c.1503A>C (p.Glu501Asp) c.2697A>C (p.Glu899Asp) | |
9 | g.91723789T>A | CA373793260 | ROR2 | c.2705A>T (p.Glu902Val) c.1920+365A>T (n.1920+365A>T) n.3173A>T c.2285A>T (p.Glu762Val) c.1502A>T (p.Glu501Val) c.2696A>T (p.Glu899Val) | |
9 | g.91723789T>C | CA373793258 | ROR2 | c.2705A>G (p.Glu902Gly) c.1920+365A>G (n.1920+365A>G) n.3173A>G c.2285A>G (p.Glu762Gly) c.1502A>G (p.Glu501Gly) c.2696A>G (p.Glu899Gly) | |
9 | g.91723789T>G | CA373793259 | ROR2 | c.2705A>C (p.Glu902Ala) c.1920+365A>C (n.1920+365A>C) n.3173A>C c.2285A>C (p.Glu762Ala) c.1502A>C (p.Glu501Ala) c.2696A>C (p.Glu899Ala) | gnomAD v4 |
9 | g.91723790C>A | CA373793261 | ROR2 | c.2704G>T (p.Glu902Ter) c.1920+364G>T (n.1920+364G>T) n.3172G>T c.2284G>T (p.Glu762Ter) c.1501G>T (p.Glu501Ter) c.2695G>T (p.Glu899Ter) | gnomAD v4 |
9 | g.91723790C>G | CA373793262 | ROR2 | c.2704G>C (p.Glu902Gln) c.1920+364G>C (n.1920+364G>C) n.3172G>C c.2284G>C (p.Glu762Gln) c.1501G>C (p.Glu501Gln) c.2695G>C (p.Glu899Gln) | |
9 | g.91723790C>T | CA373793263 | ROR2 | c.2704G>A (p.Glu902Lys) c.1920+364G>A (n.1920+364G>A) n.3172G>A c.2284G>A (p.Glu762Lys) c.1501G>A (p.Glu501Lys) c.2695G>A (p.Glu899Lys) | |
9 | g.91723791T>A | CA466334447 | ROR2 | c.2703A>T (p.Pro901=) c.1920+363A>T (n.1920+363A>T) n.3171A>T c.2283A>T (p.Pro761=) c.1500A>T (p.Pro500=) c.2694A>T (p.Pro898=) | |
9 | g.91723791T>C | CA466334448 | ROR2 | c.2703A>G (p.Pro901=) c.1920+363A>G (n.1920+363A>G) n.3171A>G c.2283A>G (p.Pro761=) c.1500A>G (p.Pro500=) c.2694A>G (p.Pro898=) | dbSNP gnomAD v4 |
9 | g.91723791T>G | CA466334449 | ROR2 | c.2703A>C (p.Pro901=) c.1920+363A>C (n.1920+363A>C) n.3171A>C c.2283A>C (p.Pro761=) c.1500A>C (p.Pro500=) c.2694A>C (p.Pro898=) | |
9 | g.91723791T= | CA1863921586 | ROR2 | c.2703A= (p.Pro901=) c.1920+363A= (n.1920+363A=) n.3171A= c.2283A= (p.Pro761=) c.1500A= (p.Pro500=) c.2694A= (p.Pro898=) |