| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.214657274A= | CA1139796882 | CENPF | c.8650A= (p.Arg2884=) n.926A= c.8827A= (p.Arg2943=) n.598A= c.7762A= (p.Arg2588=) | |
| 1 | g.214657274A>C | CA423429891 | CENPF | c.8650A>C (p.Arg2884=) n.926A>C c.8827A>C (p.Arg2943=) n.598A>C c.7762A>C (p.Arg2588=) | dbSNP |
| 1 | g.214657274A>G | CA1391504 | CENPF | c.8650A>G (p.Arg2884Gly) n.926A>G c.8827A>G (p.Arg2943Gly) n.598A>G c.7762A>G (p.Arg2588Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657274A>T | CA344857301 | CENPF | c.8650A>T (p.Arg2884Ter) n.926A>T c.8827A>T (p.Arg2943Ter) n.598A>T c.7762A>T (p.Arg2588Ter) | dbSNP |
| 1 | g.214657275G>A | CA344857303 | CENPF | c.8651G>A (p.Arg2884Lys) n.927G>A c.8828G>A (p.Arg2943Lys) n.599G>A c.7763G>A (p.Arg2588Lys) | |
| 1 | g.214657275G>C | CA344857305 | CENPF | c.8651G>C (p.Arg2884Thr) n.927G>C c.8828G>C (p.Arg2943Thr) n.599G>C c.7763G>C (p.Arg2588Thr) | |
| 1 | g.214657275G>T | CA344857307 | CENPF | c.8651G>T (p.Arg2884Ile) n.927G>T c.8828G>T (p.Arg2943Ile) n.599G>T c.7763G>T (p.Arg2588Ile) | |
| 1 | g.214657276A>C | CA344857309 | CENPF | c.8652A>C (p.Arg2884Ser) n.928A>C c.8829A>C (p.Arg2943Ser) n.600A>C c.7764A>C (p.Arg2588Ser) | gnomAD v4 |
| 1 | g.214657276A>G | CA423429897 | CENPF | c.8652A>G (p.Arg2884=) n.928A>G c.8829A>G (p.Arg2943=) n.600A>G c.7764A>G (p.Arg2588=) | |
| 1 | g.214657276A>T | CA344857310 | CENPF | c.8652A>T (p.Arg2884Ser) n.928A>T c.8829A>T (p.Arg2943Ser) n.600A>T c.7764A>T (p.Arg2588Ser) | |
| 1 | g.214657277G>A | CA344857314 | CENPF | c.8653G>A (p.Gly2885Arg) n.929G>A c.8830G>A (p.Gly2944Arg) n.601G>A c.7765G>A (p.Gly2589Arg) | |
| 1 | g.214657277G>C | CA344857316 | CENPF | c.8653G>C (p.Gly2885Arg) n.929G>C c.8830G>C (p.Gly2944Arg) n.601G>C c.7765G>C (p.Gly2589Arg) | |
| 1 | g.214657277G>T | CA344857317 | CENPF | c.8653G>T (p.Gly2885Ter) n.929G>T c.8830G>T (p.Gly2944Ter) n.601G>T c.7765G>T (p.Gly2589Ter) | |
| 1 | g.214657278G>A | CA344857319 | CENPF | c.8654G>A (p.Gly2885Glu) n.930G>A c.8831G>A (p.Gly2944Glu) n.602G>A c.7766G>A (p.Gly2589Glu) | |
| 1 | g.214657278G>C | CA344857320 | CENPF | c.8654G>C (p.Gly2885Ala) n.930G>C c.8831G>C (p.Gly2944Ala) n.602G>C c.7766G>C (p.Gly2589Ala) | |
| 1 | g.214657278G>T | CA344857322 | CENPF | c.8654G>T (p.Gly2885Val) n.930G>T c.8831G>T (p.Gly2944Val) n.602G>T c.7766G>T (p.Gly2589Val) | |
| 1 | g.214657279A>C | CA423429901 | CENPF | c.8655A>C (p.Gly2885=) n.931A>C c.8832A>C (p.Gly2944=) n.603A>C c.7767A>C (p.Gly2589=) | |
| 1 | g.214657279A>G | CA423429902 | CENPF | c.8655A>G (p.Gly2885=) n.931A>G c.8832A>G (p.Gly2944=) n.603A>G c.7767A>G (p.Gly2589=) | |
| 1 | g.214657279A>T | CA423429903 | CENPF | c.8655A>T (p.Gly2885=) n.931A>T c.8832A>T (p.Gly2944=) n.603A>T c.7767A>T (p.Gly2589=) | |
| 1 | g.214657280C>A | CA344857323 | CENPF | c.8656C>A (p.Pro2886Thr) n.932C>A c.8833C>A (p.Pro2945Thr) n.604C>A c.7768C>A (p.Pro2590Thr) | |
| 1 | g.214657280C>G | CA344857324 | CENPF | c.8656C>G (p.Pro2886Ala) n.932C>G c.8833C>G (p.Pro2945Ala) n.604C>G c.7768C>G (p.Pro2590Ala) | |
| 1 | g.214657280C>T | CA344857325 | CENPF | c.8656C>T (p.Pro2886Ser) n.932C>T c.8833C>T (p.Pro2945Ser) n.604C>T c.7768C>T (p.Pro2590Ser) | gnomAD v4 |
| 1 | g.214657281C>A | CA37381331 | CENPF | c.8657C>A (p.Pro2886Gln) n.933C>A c.8834C>A (p.Pro2945Gln) n.605C>A c.7769C>A (p.Pro2590Gln) | dbSNP gnomAD v4 |
| 1 | g.214657281C= | CA2486377678 | CENPF | c.8657C= (p.Pro2886=) n.933C= c.8834C= (p.Pro2945=) n.605C= c.7769C= (p.Pro2590=) | |
| 1 | g.214657281C>G | CA344857326 | CENPF | c.8657C>G (p.Pro2886Arg) n.933C>G c.8834C>G (p.Pro2945Arg) n.605C>G c.7769C>G (p.Pro2590Arg) | |
| 1 | g.214657281C>T | CA344857327 | CENPF | c.8657C>T (p.Pro2886Leu) n.933C>T c.8834C>T (p.Pro2945Leu) n.605C>T c.7769C>T (p.Pro2590Leu) | |
| 1 | g.214657282A>C | CA423429402 | CENPF | c.8658A>C (p.Pro2886=) n.934A>C c.8835A>C (p.Pro2945=) n.606A>C c.7770A>C (p.Pro2590=) | |
| 1 | g.214657282A>G | CA423429403 | CENPF | c.8658A>G (p.Pro2886=) n.934A>G c.8835A>G (p.Pro2945=) n.606A>G c.7770A>G (p.Pro2590=) | gnomAD v4 |
| 1 | g.214657282A>T | CA423429404 | CENPF | c.8658A>T (p.Pro2886=) n.934A>T c.8835A>T (p.Pro2945=) n.606A>T c.7770A>T (p.Pro2590=) | |
| 1 | g.214657283A= | CA2486377679 | CENPF | c.8659A= (p.Thr2887=) n.935A= c.8836A= (p.Thr2946=) n.607A= c.7771A= (p.Thr2591=) | |
| 1 | g.214657283A>C | CA344857330 | CENPF | c.8659A>C (p.Thr2887Pro) n.935A>C c.8836A>C (p.Thr2946Pro) n.607A>C c.7771A>C (p.Thr2591Pro) | |
| 1 | g.214657283A>G | CA344857331 | CENPF | c.8659A>G (p.Thr2887Ala) n.935A>G c.8836A>G (p.Thr2946Ala) n.607A>G c.7771A>G (p.Thr2591Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.214657283A>T | CA344857329 | CENPF | c.8659A>T (p.Thr2887Ser) n.935A>T c.8836A>T (p.Thr2946Ser) n.607A>T c.7771A>T (p.Thr2591Ser) | |
| 1 | g.214657284C>A | CA344857333 | CENPF | c.8660C>A (p.Thr2887Lys) n.936C>A c.8837C>A (p.Thr2946Lys) n.608C>A c.7772C>A (p.Thr2591Lys) | |
| 1 | g.214657284C>G | CA344857335 | CENPF | c.8660C>G (p.Thr2887Arg) n.936C>G c.8837C>G (p.Thr2946Arg) n.608C>G c.7772C>G (p.Thr2591Arg) | |
| 1 | g.214657284C>T | CA344857337 | CENPF | c.8660C>T (p.Thr2887Ile) n.936C>T c.8837C>T (p.Thr2946Ile) n.608C>T c.7772C>T (p.Thr2591Ile) | gnomAD v4 |
| 1 | g.214657285A= | CA2486377680 | CENPF | c.8661A= (p.Thr2887=) n.937A= c.8838A= (p.Thr2946=) n.609A= c.7773A= (p.Thr2591=) | |
| 1 | g.214657285A>C | CA423429407 | CENPF | c.8661A>C (p.Thr2887=) n.937A>C c.8838A>C (p.Thr2946=) n.609A>C c.7773A>C (p.Thr2591=) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.214657285A>G | CA1391505 | CENPF | c.8661A>G (p.Thr2887=) n.937A>G c.8838A>G (p.Thr2946=) n.609A>G c.7773A>G (p.Thr2591=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657285A>T | CA423429408 | CENPF | c.8661A>T (p.Thr2887=) n.937A>T c.8838A>T (p.Thr2946=) n.609A>T c.7773A>T (p.Thr2591=) | |
| 1 | g.214657286C>A | CA1391506 | CENPF | c.8662C>A (p.Pro2888Thr) n.938C>A c.8839C>A (p.Pro2947Thr) n.610C>A c.7774C>A (p.Pro2592Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657286C= | CA1147239407 | CENPF | c.8662C= (p.Pro2888=) n.938C= c.8839C= (p.Pro2947=) n.610C= c.7774C= (p.Pro2592=) | |
| 1 | g.214657286C>G | CA344857339 | CENPF | c.8662C>G (p.Pro2888Ala) n.938C>G c.8839C>G (p.Pro2947Ala) n.610C>G c.7774C>G (p.Pro2592Ala) | |
| 1 | g.214657286C>T | CA344857338 | CENPF | c.8662C>T (p.Pro2888Ser) n.938C>T c.8839C>T (p.Pro2947Ser) n.610C>T c.7774C>T (p.Pro2592Ser) | gnomAD v4 |
| 1 | g.214657287C>A | CA344857342 | CENPF | c.8663C>A (p.Pro2888His) n.939C>A c.8840C>A (p.Pro2947His) n.611C>A c.7775C>A (p.Pro2592His) | |
| 1 | g.214657287C>G | CA344857344 | CENPF | c.8663C>G (p.Pro2888Arg) n.939C>G c.8840C>G (p.Pro2947Arg) n.611C>G c.7775C>G (p.Pro2592Arg) | |
| 1 | g.214657287C>T | CA344857346 | CENPF | c.8663C>T (p.Pro2888Leu) n.939C>T c.8840C>T (p.Pro2947Leu) n.611C>T c.7775C>T (p.Pro2592Leu) | |
| 1 | g.214657288T>A | CA423429418 | CENPF | c.8664T>A (p.Pro2888=) n.940T>A c.8841T>A (p.Pro2947=) n.612T>A c.7776T>A (p.Pro2592=) | |
| 1 | g.214657288T>C | CA423429421 | CENPF | c.8664T>C (p.Pro2888=) n.940T>C c.8841T>C (p.Pro2947=) n.612T>C c.7776T>C (p.Pro2592=) | |
| 1 | g.214657288T>G | CA423429420 | CENPF | c.8664T>G (p.Pro2888=) n.940T>G c.8841T>G (p.Pro2947=) n.612T>G c.7776T>G (p.Pro2592=) |