Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.16948752G>A | CA8414016 | TNFRSF13B | c.431C>T (p.Ser144Leu) n.434C>T n.335C>T c.293C>T (p.Ser98Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948752G>C | CA8414017 | TNFRSF13B | c.431C>G (p.Ser144Ter) n.434C>G n.335C>G c.293C>G (p.Ser98Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948752G= | CA2250304356 | TNFRSF13B | c.431C= (p.Ser144=) n.434C= n.335C= c.293C= (p.Ser98=) | |
17 | g.16948752G>T | CA117397 | TNFRSF13B | c.431C>A (p.Ser144Ter) n.434C>A n.335C>A c.293C>A (p.Ser98Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948753A= | CA2250304371 | TNFRSF13B | c.430T= (p.Ser144=) n.433T= n.334T= c.292T= (p.Ser98=) | |
17 | g.16948753A>C | CA398519761 | TNFRSF13B | c.430T>G (p.Ser144Ala) n.433T>G n.334T>G c.292T>G (p.Ser98Ala) | |
17 | g.16948753A>G | CA398519762 | TNFRSF13B | c.430T>C (p.Ser144Pro) n.433T>C n.334T>C c.292T>C (p.Ser98Pro) | gnomAD v4 |
17 | g.16948753A>T | CA398519763 | TNFRSF13B | c.430T>A (p.Ser144Thr) n.433T>A n.334T>A c.292T>A (p.Ser98Thr) | dbSNP |
17 | g.16948754G>A | CA498420118 | TNFRSF13B | c.429C>T (p.Gly143=) n.432C>T n.333C>T c.291C>T (p.Gly97=) | |
17 | g.16948754G>C | CA498420120 | TNFRSF13B | c.429C>G (p.Gly143=) n.432C>G n.333C>G c.291C>G (p.Gly97=) | |
17 | g.16948754G>T | CA498420119 | TNFRSF13B | c.429C>A (p.Gly143=) n.432C>A n.333C>A c.291C>A (p.Gly97=) | |
17 | g.16948755C>A | CA398519766 | TNFRSF13B | c.428G>T (p.Gly143Val) n.431G>T n.332G>T c.290G>T (p.Gly97Val) | |
17 | g.16948755C= | CA2250304383 | TNFRSF13B | c.428G= (p.Gly143=) n.431G= n.332G= c.290G= (p.Gly97=) | |
17 | g.16948755C>G | CA398519764 | TNFRSF13B | c.428G>C (p.Gly143Ala) n.431G>C n.332G>C c.290G>C (p.Gly97Ala) | |
17 | g.16948755C>T | CA398519765 | TNFRSF13B | c.428G>A (p.Gly143Asp) n.431G>A n.332G>A c.290G>A (p.Gly97Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948756C>A | CA398519767 | TNFRSF13B | c.427G>T (p.Gly143Cys) n.430G>T n.331G>T c.289G>T (p.Gly97Cys) | |
17 | g.16948756C= | CA2250304387 | TNFRSF13B | c.427G= (p.Gly143=) n.430G= n.331G= c.289G= (p.Gly97=) | |
17 | g.16948756C>G | CA398519768 | TNFRSF13B | c.427G>C (p.Gly143Arg) n.430G>C n.331G>C c.289G>C (p.Gly97Arg) | gnomAD v4 COSMIC COSMIC |
17 | g.16948756C>T | CA8414018 | TNFRSF13B | c.427G>A (p.Gly143Ser) n.430G>A n.331G>A c.289G>A (p.Gly97Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.16948757T>A | CA398519769 | TNFRSF13B | c.426A>T (p.Arg142Ser) n.429A>T n.330A>T c.288A>T (p.Arg96Ser) | |
17 | g.16948757T>C | CA498420122 | TNFRSF13B | c.426A>G (p.Arg142=) n.429A>G n.330A>G c.288A>G (p.Arg96=) | |
17 | g.16948757T>G | CA398519770 | TNFRSF13B | c.426A>C (p.Arg142Ser) n.429A>C n.330A>C c.288A>C (p.Arg96Ser) | |
17 | g.16948757dup | CA625313744 | TNFRSF13B | c.426dup (p.Gly143ArgfsTer?) n.429dup n.330dup c.288dup (p.Gly97ArgfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.16948758C>A | CA398519771 | TNFRSF13B | c.425G>T (p.Arg142Ile) n.428G>T n.329G>T c.287G>T (p.Arg96Ile) | |
17 | g.16948758C>G | CA398519772 | TNFRSF13B | c.425G>C (p.Arg142Thr) n.428G>C n.329G>C c.287G>C (p.Arg96Thr) | ClinVar |
17 | g.16948758C>T | CA398519773 | TNFRSF13B | c.425G>A (p.Arg142Lys) n.428G>A n.329G>A c.287G>A (p.Arg96Lys) | |
17 | g.16948759T>A | CA398519774 | TNFRSF13B | c.424A>T (p.Arg142Ter) n.427A>T n.328A>T c.286A>T (p.Arg96Ter) | |
17 | g.16948759T>C | CA398519775 | TNFRSF13B | c.424A>G (p.Arg142Gly) n.427A>G n.328A>G c.286A>G (p.Arg96Gly) | |
17 | g.16948759T>G | CA498420125 | TNFRSF13B | c.424A>C (p.Arg142=) n.427A>C n.328A>C c.286A>C (p.Arg96=) | |
17 | g.16948760G>A | CA498420127 | TNFRSF13B | c.423C>T (p.His141=) n.426C>T n.327C>T c.285C>T (p.His95=) | |
17 | g.16948760G>C | CA398519776 | TNFRSF13B | c.423C>G (p.His141Gln) n.426C>G n.327C>G c.285C>G (p.His95Gln) | |
17 | g.16948760G>T | CA398519777 | TNFRSF13B | c.423C>A (p.His141Gln) n.426C>A n.327C>A c.285C>A (p.His95Gln) | |
17 | g.16948761T>A | CA398519778 | TNFRSF13B | c.422A>T (p.His141Leu) n.425A>T n.326A>T c.284A>T (p.His95Leu) | |
17 | g.16948761T>C | CA398519780 | TNFRSF13B | c.422A>G (p.His141Arg) n.425A>G n.326A>G c.284A>G (p.His95Arg) | gnomAD v4 |
17 | g.16948761T>G | CA398519779 | TNFRSF13B | c.422A>C (p.His141Pro) n.425A>C n.326A>C c.284A>C (p.His95Pro) | |
17 | g.16948762G>A | CA398519781 | TNFRSF13B | c.421C>T (p.His141Tyr) n.424C>T n.325C>T c.283C>T (p.His95Tyr) | |
17 | g.16948762G>C | CA398519782 | TNFRSF13B | c.421C>G (p.His141Asp) n.424C>G n.325C>G c.283C>G (p.His95Asp) | |
17 | g.16948762G>T | CA398519783 | TNFRSF13B | c.421C>A (p.His141Asn) n.424C>A n.325C>A c.283C>A (p.His95Asn) | |
17 | g.16948763C>A | CA398519784 | TNFRSF13B | c.420G>T (p.Glu140Asp) n.423G>T n.324G>T c.282G>T (p.Glu94Asp) | |
17 | g.16948763C>G | CA398519785 | TNFRSF13B | c.420G>C (p.Glu140Asp) n.423G>C n.324G>C c.282G>C (p.Glu94Asp) | |
17 | g.16948763C>T | CA498420131 | TNFRSF13B | c.420G>A (p.Glu140=) n.423G>A n.324G>A c.282G>A (p.Glu94=) | gnomAD v4 |
17 | g.16948764T>A | CA398519786 | TNFRSF13B | c.419A>T (p.Glu140Val) n.422A>T n.323A>T c.281A>T (p.Glu94Val) | |
17 | g.16948764T>C | CA288287921 | TNFRSF13B | c.419A>G (p.Glu140Gly) n.422A>G n.323A>G c.281A>G (p.Glu94Gly) | dbSNP |
17 | g.16948764T>G | CA398519787 | TNFRSF13B | c.419A>C (p.Glu140Ala) n.422A>C n.323A>C c.281A>C (p.Glu94Ala) | |
17 | g.16948764T= | CA2250304394 | TNFRSF13B | c.419A= (p.Glu140=) n.422A= n.323A= c.281A= (p.Glu94=) | |
17 | g.16948765C>A | CA398519788 | TNFRSF13B | c.418G>T (p.Glu140Ter) n.421G>T n.322G>T c.280G>T (p.Glu94Ter) | gnomAD v4 |
17 | g.16948765C= | CA2250304397 | TNFRSF13B | c.418G= (p.Glu140=) n.421G= n.322G= c.280G= (p.Glu94=) | |
17 | g.16948765C>G | CA398519789 | TNFRSF13B | c.418G>C (p.Glu140Gln) n.421G>C n.322G>C c.280G>C (p.Glu94Gln) | |
17 | g.16948765C>T | CA8414019 | TNFRSF13B | c.418G>A (p.Glu140Lys) n.421G>A n.322G>A c.280G>A (p.Glu94Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948766C>A | CA398519790 | TNFRSF13B | c.417G>T (p.Leu139Phe) n.420G>T n.321G>T c.279G>T (p.Leu93Phe) |