Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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=) | |
1 | g.214657289G>A | CA344857348 | CENPF | c.8665G>A (p.Ala2889Thr) n.941G>A c.8842G>A (p.Ala2948Thr) n.613G>A c.7777G>A (p.Ala2593Thr) | |
1 | g.214657289G>C | CA344857349 | CENPF | c.8665G>C (p.Ala2889Pro) n.941G>C c.8842G>C (p.Ala2948Pro) n.613G>C c.7777G>C (p.Ala2593Pro) | |
1 | g.214657289G>T | CA344857351 | CENPF | c.8665G>T (p.Ala2889Ser) n.941G>T c.8842G>T (p.Ala2948Ser) n.613G>T c.7777G>T (p.Ala2593Ser) | |
1 | g.214657290C>A | CA344857353 | CENPF | c.8666C>A (p.Ala2889Asp) n.942C>A c.8843C>A (p.Ala2948Asp) n.614C>A c.7778C>A (p.Ala2593Asp) | |
1 | g.214657290C>G | CA344857356 | CENPF | c.8666C>G (p.Ala2889Gly) n.942C>G c.8843C>G (p.Ala2948Gly) n.614C>G c.7778C>G (p.Ala2593Gly) | |
1 | g.214657290C>T | CA344857355 | CENPF | c.8666C>T (p.Ala2889Val) n.942C>T c.8843C>T (p.Ala2948Val) n.614C>T c.7778C>T (p.Ala2593Val) | |
1 | g.214657291T>A | CA423429430 | CENPF | c.8667T>A (p.Ala2889=) n.943T>A c.8844T>A (p.Ala2948=) n.615T>A c.7779T>A (p.Ala2593=) | |
1 | g.214657291T>C | CA423429427 | CENPF | c.8667T>C (p.Ala2889=) n.943T>C c.8844T>C (p.Ala2948=) n.615T>C c.7779T>C (p.Ala2593=) | gnomAD v4 |
1 | g.214657291T>G | CA423429425 | CENPF | c.8667T>G (p.Ala2889=) n.943T>G c.8844T>G (p.Ala2948=) n.615T>G c.7779T>G (p.Ala2593=) | |
1 | g.214657292A= | CA2486377681 | CENPF | c.8668A= (p.Thr2890=) n.944A= c.8845A= (p.Thr2949=) n.616A= c.7780A= (p.Thr2594=) | |
1 | g.214657292A>C | CA344857357 | CENPF | c.8668A>C (p.Thr2890Pro) n.944A>C c.8845A>C (p.Thr2949Pro) n.616A>C c.7780A>C (p.Thr2594Pro) | |
1 | g.214657292A>G | CA1391507 | CENPF | c.8668A>G (p.Thr2890Ala) n.944A>G c.8845A>G (p.Thr2949Ala) n.616A>G c.7780A>G (p.Thr2594Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.214657292A>T | CA344857359 | CENPF | c.8668A>T (p.Thr2890Ser) n.944A>T c.8845A>T (p.Thr2949Ser) n.616A>T c.7780A>T (p.Thr2594Ser) | |
1 | g.214657293C>A | CA344857362 | CENPF | c.8669C>A (p.Thr2890Asn) n.945C>A c.8846C>A (p.Thr2949Asn) n.617C>A c.7781C>A (p.Thr2594Asn) | gnomAD v4 |
1 | g.214657293C>G | CA344857365 | CENPF | c.8669C>G (p.Thr2890Ser) n.945C>G c.8846C>G (p.Thr2949Ser) n.617C>G c.7781C>G (p.Thr2594Ser) | |
1 | g.214657293C>T | CA344857363 | CENPF | c.8669C>T (p.Thr2890Ile) n.945C>T c.8846C>T (p.Thr2949Ile) n.617C>T c.7781C>T (p.Thr2594Ile) | |
1 | g.214657294C>A | CA423429432 | CENPF | c.8670C>A (p.Thr2890=) n.946C>A c.8847C>A (p.Thr2949=) n.618C>A c.7782C>A (p.Thr2594=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657294C= | CA2486377682 | CENPF | c.8670C= (p.Thr2890=) n.946C= c.8847C= (p.Thr2949=) n.618C= c.7782C= (p.Thr2594=) | |
1 | g.214657294C>G | CA423429436 | CENPF | c.8670C>G (p.Thr2890=) n.946C>G c.8847C>G (p.Thr2949=) n.618C>G c.7782C>G (p.Thr2594=) | dbSNP gnomAD v4 |
1 | g.214657294C>T | CA423429433 | CENPF | c.8670C>T (p.Thr2890=) n.946C>T c.8847C>T (p.Thr2949=) n.618C>T c.7782C>T (p.Thr2594=) | gnomAD v4 |
1 | g.214657295C>A | CA344857367 | CENPF | c.8671C>A (p.Pro2891Thr) n.947C>A c.8848C>A (p.Pro2950Thr) n.619C>A c.7783C>A (p.Pro2595Thr) | |
1 | g.214657295C>G | CA344857371 | CENPF | c.8671C>G (p.Pro2891Ala) n.947C>G c.8848C>G (p.Pro2950Ala) n.619C>G c.7783C>G (p.Pro2595Ala) | |
1 | g.214657295C>T | CA344857369 | CENPF | c.8671C>T (p.Pro2891Ser) n.947C>T c.8848C>T (p.Pro2950Ser) n.619C>T c.7783C>T (p.Pro2595Ser) | |
1 | g.214657296C>A | CA344857372 | CENPF | c.8672C>A (p.Pro2891Gln) n.948C>A c.8849C>A (p.Pro2950Gln) n.620C>A c.7784C>A (p.Pro2595Gln) | |
1 | g.214657296C>G | CA344857374 | CENPF | c.8672C>G (p.Pro2891Arg) n.948C>G c.8849C>G (p.Pro2950Arg) n.620C>G c.7784C>G (p.Pro2595Arg) | |
1 | g.214657296C>T | CA344857376 | CENPF | c.8672C>T (p.Pro2891Leu) n.948C>T c.8849C>T (p.Pro2950Leu) n.620C>T c.7784C>T (p.Pro2595Leu) | gnomAD v4 |
1 | g.214657296_214657298delinsCAG | CA2486377683 | CENPF | c.8672_8674delinsCAG (p.Pro2891=) n.948_950delinsCAG c.8849_8851delinsCAG (p.Pro2950=) n.620_622delinsCAG c.7784_7786delinsCAG (p.Pro2595=) | |
1 | g.214657297A= | CA2486377684 | CENPF | c.8673A= (p.Pro2891=) n.949A= c.8850A= (p.Pro2950=) n.621A= c.7785A= (p.Pro2595=) | |
1 | g.214657297A>C | CA423429440 | CENPF | c.8673A>C (p.Pro2891=) n.949A>C c.8850A>C (p.Pro2950=) n.621A>C c.7785A>C (p.Pro2595=) | gnomAD v4 |
1 | g.214657297A>G | CA1391508 | CENPF | c.8673A>G (p.Pro2891=) n.949A>G c.8850A>G (p.Pro2950=) n.621A>G c.7785A>G (p.Pro2595=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.214657297A>T | CA423429442 | CENPF | c.8673A>T (p.Pro2891=) n.949A>T c.8850A>T (p.Pro2950=) n.621A>T c.7785A>T (p.Pro2595=) | |
1 | g.214657301_214657302del | CA529001866 | CENPF | c.8677_8678del (p.Ser2893LeufsTer3) n.953_954del c.8854_8855del (p.Ser2952LeufsTer3) n.625_626del c.7789_7790del (p.Ser2597LeufsTer3) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657298G>A | CA1391509 | CENPF | c.8674G>A (p.Glu2892Lys) n.950G>A c.8851G>A (p.Glu2951Lys) n.622G>A c.7786G>A (p.Glu2596Lys) | dbSNP ExAC gnomAD v2 |
1 | g.214657298G>C | CA344857379 | CENPF | c.8674G>C (p.Glu2892Gln) n.950G>C c.8851G>C (p.Glu2951Gln) n.622G>C c.7786G>C (p.Glu2596Gln) | |
1 | g.214657298G= | CA1148250855 | CENPF | c.8674G= (p.Glu2892=) n.950G= c.8851G= (p.Glu2951=) n.622G= c.7786G= (p.Glu2596=) | |
1 | g.214657298G>T | CA344857382 | CENPF | c.8674G>T (p.Glu2892Ter) n.950G>T c.8851G>T (p.Glu2951Ter) n.622G>T c.7786G>T (p.Glu2596Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657299A>C | CA344857386 | CENPF | c.8675A>C (p.Glu2892Ala) n.951A>C c.8852A>C (p.Glu2951Ala) n.623A>C c.7787A>C (p.Glu2596Ala) | |
1 | g.214657299A>G | CA344857383 | CENPF | c.8675A>G (p.Glu2892Gly) n.951A>G c.8852A>G (p.Glu2951Gly) n.623A>G c.7787A>G (p.Glu2596Gly) | |
1 | g.214657299A>T | CA344857385 | CENPF | c.8675A>T (p.Glu2892Val) n.951A>T c.8852A>T (p.Glu2951Val) n.623A>T c.7787A>T (p.Glu2596Val) | |
1 | g.214657300G>A | CA423429447 | CENPF | c.8676G>A (p.Glu2892=) n.952G>A c.8853G>A (p.Glu2951=) n.624G>A c.7788G>A (p.Glu2596=) | gnomAD v4 |
1 | g.214657300G>C | CA344857387 | CENPF | c.8676G>C (p.Glu2892Asp) n.952G>C c.8853G>C (p.Glu2951Asp) n.624G>C c.7788G>C (p.Glu2596Asp) | |
1 | g.214657300G= | CA2486377685 | CENPF | c.8676G= (p.Glu2892=) n.952G= c.8853G= (p.Glu2951=) n.624G= c.7788G= (p.Glu2596=) | |
1 | g.214657300G>T | CA344857389 | CENPF | c.8676G>T (p.Glu2892Asp) n.952G>T c.8853G>T (p.Glu2951Asp) n.624G>T c.7788G>T (p.Glu2596Asp) | dbSNP gnomAD v4 |
1 | g.214657300dup | CA2840225139 | CENPF | c.8676dup (p.Ser2893GlufsTer4) n.952dup c.8853dup (p.Ser2952GlufsTer4) n.624dup c.7788dup (p.Ser2597GlufsTer4) | |
1 | g.214657301A= | CA2486377686 | CENPF | c.8677A= (p.Ser2893=) n.953A= c.8854A= (p.Ser2952=) n.625A= c.7789A= (p.Ser2597=) | |
1 | g.214657301A>C | CA344857390 | CENPF | c.8677A>C (p.Ser2893Arg) n.953A>C c.8854A>C (p.Ser2952Arg) n.625A>C c.7789A>C (p.Ser2597Arg) | |
1 | g.214657301A>G | CA344857391 | CENPF | c.8677A>G (p.Ser2893Gly) n.953A>G c.8854A>G (p.Ser2952Gly) n.625A>G c.7789A>G (p.Ser2597Gly) | |
1 | g.214657301A>T | CA344857393 | CENPF | c.8677A>T (p.Ser2893Cys) n.953A>T c.8854A>T (p.Ser2952Cys) n.625A>T c.7789A>T (p.Ser2597Cys) | |
1 | g.214657302G>A | CA344857396 | CENPF | c.8678G>A (p.Ser2893Asn) n.954G>A c.8855G>A (p.Ser2952Asn) n.626G>A c.7790G>A (p.Ser2597Asn) | |
1 | g.214657302G>C | CA1391510 | CENPF | c.8678G>C (p.Ser2893Thr) n.954G>C c.8855G>C (p.Ser2952Thr) n.626G>C c.7790G>C (p.Ser2597Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657302G= | CA1147191330 | CENPF | c.8678G= (p.Ser2893=) n.954G= c.8855G= (p.Ser2952=) n.626G= c.7790G= (p.Ser2597=) | |
1 | g.214657302G>T | CA344857395 | CENPF | c.8678G>T (p.Ser2893Ile) n.954G>T c.8855G>T (p.Ser2952Ile) n.626G>T c.7790G>T (p.Ser2597Ile) | |
1 | g.214657302_214657304dup | CA37381385 | CENPF | c.8678_8680dup (p.Ser2893_Phe2894insCys) n.954_956dup c.8855_8857dup (p.Ser2952_Phe2953insCys) n.626_628dup c.7790_7792dup (p.Ser2597_Phe2598insCys) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657303C>A | CA344857398 | CENPF | c.8679C>A (p.Ser2893Arg) n.955C>A c.8856C>A (p.Ser2952Arg) n.627C>A c.7791C>A (p.Ser2597Arg) | |
1 | g.214657303C>G | CA344857402 | CENPF | c.8679C>G (p.Ser2893Arg) n.955C>G c.8856C>G (p.Ser2952Arg) n.627C>G c.7791C>G (p.Ser2597Arg) | |
1 | g.214657303C>T | CA423429454 | CENPF | c.8679C>T (p.Ser2893=) n.955C>T c.8856C>T (p.Ser2952=) n.627C>T c.7791C>T (p.Ser2597=) | gnomAD v4 |
1 | g.214657304T>A | CA344857404 | CENPF | c.8680T>A (p.Phe2894Ile) n.956T>A c.8857T>A (p.Phe2953Ile) n.628T>A c.7792T>A (p.Phe2598Ile) | |
1 | g.214657304T>C | CA344857407 | CENPF | c.8680T>C (p.Phe2894Leu) n.956T>C c.8857T>C (p.Phe2953Leu) n.628T>C c.7792T>C (p.Phe2598Leu) | |
1 | g.214657304T>G | CA344857409 | CENPF | c.8680T>G (p.Phe2894Val) n.956T>G c.8857T>G (p.Phe2953Val) n.628T>G c.7792T>G (p.Phe2598Val) | |
1 | g.214657305T>A | CA344857412 | CENPF | c.8681T>A (p.Phe2894Tyr) n.957T>A c.8858T>A (p.Phe2953Tyr) n.629T>A c.7793T>A (p.Phe2598Tyr) | |
1 | g.214657305T>C | CA344857413 | CENPF | c.8681T>C (p.Phe2894Ser) n.957T>C c.8858T>C (p.Phe2953Ser) n.629T>C c.7793T>C (p.Phe2598Ser) | |
1 | g.214657305T>G | CA344857415 | CENPF | c.8681T>G (p.Phe2894Cys) n.957T>G c.8858T>G (p.Phe2953Cys) n.629T>G c.7793T>G (p.Phe2598Cys) | |
1 | g.214657306T>A | CA344857417 | CENPF | c.8682T>A (p.Phe2894Leu) n.958T>A c.8859T>A (p.Phe2953Leu) n.630T>A c.7794T>A (p.Phe2598Leu) | |
1 | g.214657306T>C | CA423429458 | CENPF | c.8682T>C (p.Phe2894=) n.958T>C c.8859T>C (p.Phe2953=) n.630T>C c.7794T>C (p.Phe2598=) | |
1 | g.214657306T>G | CA344857418 | CENPF | c.8682T>G (p.Phe2894Leu) n.958T>G c.8859T>G (p.Phe2953Leu) n.630T>G c.7794T>G (p.Phe2598Leu) | |
1 | g.214657307T>A | CA344857420 | CENPF | c.8683T>A (p.Ser2895Thr) n.959T>A c.8860T>A (p.Ser2954Thr) n.631T>A c.7795T>A (p.Ser2599Thr) | |
1 | g.214657307T>C | CA344857422 | CENPF | c.8683T>C (p.Ser2895Pro) n.959T>C c.8860T>C (p.Ser2954Pro) n.631T>C c.7795T>C (p.Ser2599Pro) | dbSNP |
1 | g.214657307T>G | CA344857421 | CENPF | c.8683T>G (p.Ser2895Ala) n.959T>G c.8860T>G (p.Ser2954Ala) n.631T>G c.7795T>G (p.Ser2599Ala) | |
1 | g.214657307T= | CA2486377687 | CENPF | c.8683T= (p.Ser2895=) n.959T= c.8860T= (p.Ser2954=) n.631T= c.7795T= (p.Ser2599=) | |
1 | g.214657308C>A | CA344857423 | CENPF | c.8684C>A (p.Ser2895Tyr) n.960C>A c.8861C>A (p.Ser2954Tyr) n.632C>A c.7796C>A (p.Ser2599Tyr) | |
1 | g.214657308C>G | CA344857424 | CENPF | c.8684C>G (p.Ser2895Cys) n.960C>G c.8861C>G (p.Ser2954Cys) n.632C>G c.7796C>G (p.Ser2599Cys) | |
1 | g.214657308C>T | CA344857427 | CENPF | c.8684C>T (p.Ser2895Phe) n.960C>T c.8861C>T (p.Ser2954Phe) n.632C>T c.7796C>T (p.Ser2599Phe) | gnomAD v4 |
1 | g.214657309T>A | CA423429460 | CENPF | c.8685T>A (p.Ser2895=) n.961T>A c.8862T>A (p.Ser2954=) n.633T>A c.7797T>A (p.Ser2599=) | |
1 | g.214657309T>C | CA423429463 | CENPF | c.8685T>C (p.Ser2895=) n.961T>C c.8862T>C (p.Ser2954=) n.633T>C c.7797T>C (p.Ser2599=) | |
1 | g.214657309T>G | CA423429462 | CENPF | c.8685T>G (p.Ser2895=) n.961T>G c.8862T>G (p.Ser2954=) n.633T>G c.7797T>G (p.Ser2599=) | gnomAD v4 |
1 | g.214657309T= | CA2486377688 | CENPF | c.8685T= (p.Ser2895=) n.961T= c.8862T= (p.Ser2954=) n.633T= c.7797T= (p.Ser2599=) | |
1 | g.214657310A>C | CA344857429 | CENPF | c.8686A>C (p.Lys2896Gln) n.962A>C c.8863A>C (p.Lys2955Gln) n.634A>C c.7798A>C (p.Lys2600Gln) | |
1 | g.214657310A>G | CA344857432 | CENPF | c.8686A>G (p.Lys2896Glu) n.962A>G c.8863A>G (p.Lys2955Glu) n.634A>G c.7798A>G (p.Lys2600Glu) | |
1 | g.214657310A>T | CA344857434 | CENPF | c.8686A>T (p.Lys2896Ter) n.962A>T c.8863A>T (p.Lys2955Ter) n.634A>T c.7798A>T (p.Lys2600Ter) | |
1 | g.214657316_214657317insAAAAAAAAA | CA2747692471 | CENPF | c.8692_8693insAAAAAAAAA (p.Lys2897_Ser2898insLysLysLys) n.968_969insAAAAAAAAA c.8869_8870insAAAAAAAAA (p.Lys2956_Ser2957insLysLysLys) n.640_641insAAAAAAAAA c.7804_7805insAAAAAAAAA (p.Lys2601_Ser2602insLysLysLys) | |
1 | g.214657316_214657317insAAAAAAAAAA | CA2747692472 | CENPF | c.8692_8693insAAAAAAAAAA (p.Ser2898LysfsTer22) n.968_969insAAAAAAAAAA c.8869_8870insAAAAAAAAAA (p.Ser2957LysfsTer22) n.640_641insAAAAAAAAAA c.7804_7805insAAAAAAAAAA (p.Ser2602LysfsTer22) | |
1 | g.214657316dup | CA1391511 | CENPF | c.8692dup (p.Ser2898LysfsTer19) n.968dup c.8869dup (p.Ser2957LysfsTer19) n.640dup c.7804dup (p.Ser2602LysfsTer19) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.214657316del | CA423429466 | CENPF | c.8692del (p.Ser2898AlafsTer6) n.968del c.8869del (p.Ser2957AlafsTer6) n.640del c.7804del (p.Ser2602AlafsTer6) | gnomAD v2 gnomAD v4 COSMIC |
1 | g.214657315_214657316del | CA2840225140 | CENPF | c.8691_8692del (p.Ser2898GlnfsTer18) n.967_968del c.8868_8869del (p.Ser2957GlnfsTer18) n.639_640del c.7803_7804del (p.Ser2602GlnfsTer18) | |
1 | g.214657311A>C | CA344857435 | CENPF | c.8687A>C (p.Lys2896Thr) n.963A>C c.8864A>C (p.Lys2955Thr) n.635A>C c.7799A>C (p.Lys2600Thr) | |
1 | g.214657311A>G | CA344857436 | CENPF | c.8687A>G (p.Lys2896Arg) n.963A>G c.8864A>G (p.Lys2955Arg) n.635A>G c.7799A>G (p.Lys2600Arg) | |
1 | g.214657311A>T | CA344857437 | CENPF | c.8687A>T (p.Lys2896Ile) n.963A>T c.8864A>T (p.Lys2955Ile) n.635A>T c.7799A>T (p.Lys2600Ile) | |
1 | g.214657312A>C | CA344857438 | CENPF | c.8688A>C (p.Lys2896Asn) n.964A>C c.8865A>C (p.Lys2955Asn) n.636A>C c.7800A>C (p.Lys2600Asn) | |
1 | g.214657312A>G | CA423429470 | CENPF | c.8688A>G (p.Lys2896=) n.964A>G c.8865A>G (p.Lys2955=) n.636A>G c.7800A>G (p.Lys2600=) | |
1 | g.214657312A>T | CA344857439 | CENPF | c.8688A>T (p.Lys2896Asn) n.964A>T c.8865A>T (p.Lys2955Asn) n.636A>T c.7800A>T (p.Lys2600Asn) | |
1 | g.214657313A>C | CA344857442 | CENPF | c.8689A>C (p.Lys2897Gln) n.965A>C c.8866A>C (p.Lys2956Gln) n.637A>C c.7801A>C (p.Lys2601Gln) | |
1 | g.214657313A>G | CA344857440 | CENPF | c.8689A>G (p.Lys2897Glu) n.965A>G c.8866A>G (p.Lys2956Glu) n.637A>G c.7801A>G (p.Lys2601Glu) | |
1 | g.214657313A>T | CA344857441 | CENPF | c.8689A>T (p.Lys2897Ter) n.965A>T c.8866A>T (p.Lys2956Ter) n.637A>T c.7801A>T (p.Lys2601Ter) | gnomAD v4 |
1 | g.214657314A>C | CA344857443 | CENPF | c.8690A>C (p.Lys2897Thr) n.966A>C c.8867A>C (p.Lys2956Thr) n.638A>C c.7802A>C (p.Lys2601Thr) | |
1 | g.214657314A>G | CA344857444 | CENPF | c.8690A>G (p.Lys2897Arg) n.966A>G c.8867A>G (p.Lys2956Arg) n.638A>G c.7802A>G (p.Lys2601Arg) | |
1 | g.214657314A>T | CA344857445 | CENPF | c.8690A>T (p.Lys2897Ile) n.966A>T c.8867A>T (p.Lys2956Ile) n.638A>T c.7802A>T (p.Lys2601Ile) | |
1 | g.214657315A>C | CA344857446 | CENPF | c.8691A>C (p.Lys2897Asn) n.967A>C c.8868A>C (p.Lys2956Asn) n.639A>C c.7803A>C (p.Lys2601Asn) | gnomAD v4 |
1 | g.214657315A>G | CA423429474 | CENPF | c.8691A>G (p.Lys2897=) n.967A>G c.8868A>G (p.Lys2956=) n.639A>G c.7803A>G (p.Lys2601=) | |
1 | g.214657315A>T | CA344857448 | CENPF | c.8691A>T (p.Lys2897Asn) n.967A>T c.8868A>T (p.Lys2956Asn) n.639A>T c.7803A>T (p.Lys2601Asn) | |
1 | g.214657316A= | CA2486377689 | CENPF | c.8692A= (p.Ser2898=) n.968A= c.8869A= (p.Ser2957=) n.640A= c.7804A= (p.Ser2602=) | |
1 | g.214657316A>C | CA344857449 | CENPF | c.8692A>C (p.Ser2898Arg) n.968A>C c.8869A>C (p.Ser2957Arg) n.640A>C c.7804A>C (p.Ser2602Arg) | |
1 | g.214657316A>G | CA344857450 | CENPF | c.8692A>G (p.Ser2898Gly) n.968A>G c.8869A>G (p.Ser2957Gly) n.640A>G c.7804A>G (p.Ser2602Gly) | COSMIC |
1 | g.214657316A>T | CA344857451 | CENPF | c.8692A>T (p.Ser2898Cys) n.968A>T c.8869A>T (p.Ser2957Cys) n.640A>T c.7804A>T (p.Ser2602Cys) | dbSNP |
1 | g.214657317G>A | CA344857452 | CENPF | c.8693G>A (p.Ser2898Asn) n.969G>A c.8870G>A (p.Ser2957Asn) n.641G>A c.7805G>A (p.Ser2602Asn) | gnomAD v4 |
1 | g.214657317G>C | CA1391512 | CENPF | c.8693G>C (p.Ser2898Thr) n.969G>C c.8870G>C (p.Ser2957Thr) n.641G>C c.7805G>C (p.Ser2602Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657317G= | CA1144828258 | CENPF | c.8693G= (p.Ser2898=) n.969G= c.8870G= (p.Ser2957=) n.641G= c.7805G= (p.Ser2602=) | |
1 | g.214657317G>T | CA344857454 | CENPF | c.8693G>T (p.Ser2898Ile) n.969G>T c.8870G>T (p.Ser2957Ile) n.641G>T c.7805G>T (p.Ser2602Ile) | |
1 | g.214657318C>A | CA344857455 | CENPF | c.8694C>A (p.Ser2898Arg) n.970C>A c.8871C>A (p.Ser2957Arg) n.642C>A c.7806C>A (p.Ser2602Arg) | |
1 | g.214657318C>G | CA344857456 | CENPF | c.8694C>G (p.Ser2898Arg) n.970C>G c.8871C>G (p.Ser2957Arg) n.642C>G c.7806C>G (p.Ser2602Arg) | |
1 | g.214657318C>T | CA423429475 | CENPF | c.8694C>T (p.Ser2898=) n.970C>T c.8871C>T (p.Ser2957=) n.642C>T c.7806C>T (p.Ser2602=) | |
1 | g.214657319A= | CA2486377690 | CENPF | c.8695A= (p.Lys2899=) n.971A= c.8872A= (p.Lys2958=) n.643A= c.7807A= (p.Lys2603=) | |
1 | g.214657319A>C | CA344857458 | CENPF | c.8695A>C (p.Lys2899Gln) n.971A>C c.8872A>C (p.Lys2958Gln) n.643A>C c.7807A>C (p.Lys2603Gln) | gnomAD v4 |
1 | g.214657319A>G | CA344857461 | CENPF | c.8695A>G (p.Lys2899Glu) n.971A>G c.8872A>G (p.Lys2958Glu) n.643A>G c.7807A>G (p.Lys2603Glu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657319A>T | CA344857459 | CENPF | c.8695A>T (p.Lys2899Ter) n.971A>T c.8872A>T (p.Lys2958Ter) n.643A>T c.7807A>T (p.Lys2603Ter) | |
1 | g.214657320A= | CA2486377691 | CENPF | c.8696A= (p.Lys2899=) n.972A= c.8873A= (p.Lys2958=) n.644A= c.7808A= (p.Lys2603=) | |
1 | g.214657320A>C | CA344857463 | CENPF | c.8696A>C (p.Lys2899Thr) n.972A>C c.8873A>C (p.Lys2958Thr) n.644A>C c.7808A>C (p.Lys2603Thr) | |
1 | g.214657320A>G | CA344857465 | CENPF | c.8696A>G (p.Lys2899Arg) n.972A>G c.8873A>G (p.Lys2958Arg) n.644A>G c.7808A>G (p.Lys2603Arg) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657320A>T | CA344857468 | CENPF | c.8696A>T (p.Lys2899Met) n.972A>T c.8873A>T (p.Lys2958Met) n.644A>T c.7808A>T (p.Lys2603Met) | |
1 | g.214657321G>A | CA423429481 | CENPF | c.8697G>A (p.Lys2899=) n.973G>A c.8874G>A (p.Lys2958=) n.645G>A c.7809G>A (p.Lys2603=) | |
1 | g.214657321G>C | CA344857470 | CENPF | c.8697G>C (p.Lys2899Asn) n.973G>C c.8874G>C (p.Lys2958Asn) n.645G>C c.7809G>C (p.Lys2603Asn) | |
1 | g.214657321G= | CA2486377692 | CENPF | c.8697G= (p.Lys2899=) n.973G= c.8874G= (p.Lys2958=) n.645G= c.7809G= (p.Lys2603=) | |
1 | g.214657321G>T | CA344857472 | CENPF | c.8697G>T (p.Lys2899Asn) n.973G>T c.8874G>T (p.Lys2958Asn) n.645G>T c.7809G>T (p.Lys2603Asn) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.214657322A>C | CA344857473 | CENPF | c.8698A>C (p.Lys2900Gln) n.974A>C c.8875A>C (p.Lys2959Gln) n.646A>C c.7810A>C (p.Lys2604Gln) | |
1 | g.214657322A>G | CA344857475 | CENPF | c.8698A>G (p.Lys2900Glu) n.974A>G c.8875A>G (p.Lys2959Glu) n.646A>G c.7810A>G (p.Lys2604Glu) | |
1 | g.214657322A>T | CA344857476 | CENPF | c.8698A>T (p.Lys2900Ter) n.974A>T c.8875A>T (p.Lys2959Ter) n.646A>T c.7810A>T (p.Lys2604Ter) | |
1 | g.214657324dup | CA2840225141 | CENPF | c.8700dup (p.Ala2901SerfsTer16) n.976dup c.8877dup (p.Ala2960SerfsTer16) n.648dup c.7812dup (p.Ala2605SerfsTer16) | |
1 | g.214657323A>C | CA344857478 | CENPF | c.8699A>C (p.Lys2900Thr) n.975A>C c.8876A>C (p.Lys2959Thr) n.647A>C c.7811A>C (p.Lys2604Thr) | |
1 | g.214657323A>G | CA344857479 | CENPF | c.8699A>G (p.Lys2900Arg) n.975A>G c.8876A>G (p.Lys2959Arg) n.647A>G c.7811A>G (p.Lys2604Arg) | |
1 | g.214657323A>T | CA344857480 | CENPF | c.8699A>T (p.Lys2900Ile) n.975A>T c.8876A>T (p.Lys2959Ile) n.647A>T c.7811A>T (p.Lys2604Ile) | |
1 | g.214657324A>C | CA344857485 | CENPF | c.8700A>C (p.Lys2900Asn) n.976A>C c.8877A>C (p.Lys2959Asn) n.648A>C c.7812A>C (p.Lys2604Asn) | |
1 | g.214657324A>G | CA423429486 | CENPF | c.8700A>G (p.Lys2900=) n.976A>G c.8877A>G (p.Lys2959=) n.648A>G c.7812A>G (p.Lys2604=) | |
1 | g.214657324A>T | CA344857487 | CENPF | c.8700A>T (p.Lys2900Asn) n.976A>T c.8877A>T (p.Lys2959Asn) n.648A>T c.7812A>T (p.Lys2604Asn) | |
1 | g.214657325G>A | CA344857489 | CENPF | c.8701G>A (p.Ala2901Thr) n.977G>A c.8878G>A (p.Ala2960Thr) n.649G>A c.7813G>A (p.Ala2605Thr) | gnomAD v4 |
1 | g.214657325G>C | CA344857492 | CENPF | c.8701G>C (p.Ala2901Pro) n.977G>C c.8878G>C (p.Ala2960Pro) n.649G>C c.7813G>C (p.Ala2605Pro) | |
1 | g.214657325G>T | CA344857491 | CENPF | c.8701G>T (p.Ala2901Ser) n.977G>T c.8878G>T (p.Ala2960Ser) n.649G>T c.7813G>T (p.Ala2605Ser) | |
1 | g.214657326C>A | CA344857494 | CENPF | c.8702C>A (p.Ala2901Glu) n.978C>A c.8879C>A (p.Ala2960Glu) n.650C>A c.7814C>A (p.Ala2605Glu) | |
1 | g.214657326C>G | CA344857495 | CENPF | c.8702C>G (p.Ala2901Gly) n.978C>G c.8879C>G (p.Ala2960Gly) n.650C>G c.7814C>G (p.Ala2605Gly) | |
1 | g.214657326C>T | CA344857498 | CENPF | c.8702C>T (p.Ala2901Val) n.978C>T c.8879C>T (p.Ala2960Val) n.650C>T c.7814C>T (p.Ala2605Val) | |
1 | g.214657327A>C | CA423429492 | CENPF | c.8703A>C (p.Ala2901=) n.979A>C c.8880A>C (p.Ala2960=) n.651A>C c.7815A>C (p.Ala2605=) | |
1 | g.214657327A>G | CA423429493 | CENPF | c.8703A>G (p.Ala2901=) n.979A>G c.8880A>G (p.Ala2960=) n.651A>G c.7815A>G (p.Ala2605=) | |
1 | g.214657327A>T | CA423429494 | CENPF | c.8703A>T (p.Ala2901=) n.979A>T c.8880A>T (p.Ala2960=) n.651A>T c.7815A>T (p.Ala2605=) | |
1 | g.214657328G>A | CA1391513 | CENPF | c.8704G>A (p.Val2902Ile) n.980G>A c.8881G>A (p.Val2961Ile) n.652G>A c.7816G>A (p.Val2606Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.214657328G>C | CA344857506 | CENPF | c.8704G>C (p.Val2902Leu) n.980G>C c.8881G>C (p.Val2961Leu) n.652G>C c.7816G>C (p.Val2606Leu) | |
1 | g.214657328G= | CA1149069033 | CENPF | c.8704G= (p.Val2902=) n.980G= c.8881G= (p.Val2961=) n.652G= c.7816G= (p.Val2606=) | |
1 | g.214657328G>T | CA344857507 | CENPF | c.8704G>T (p.Val2902Phe) n.980G>T c.8881G>T (p.Val2961Phe) n.652G>T c.7816G>T (p.Val2606Phe) | gnomAD v4 COSMIC |
1 | g.214657329T>A | CA344857508 | CENPF | c.8705T>A (p.Val2902Asp) n.981T>A c.8882T>A (p.Val2961Asp) n.653T>A c.7817T>A (p.Val2606Asp) | |
1 | g.214657329T>C | CA344857510 | CENPF | c.8705T>C (p.Val2902Ala) n.981T>C c.8882T>C (p.Val2961Ala) n.653T>C c.7817T>C (p.Val2606Ala) | |
1 | g.214657329T>G | CA344857511 | CENPF | c.8705T>G (p.Val2902Gly) n.981T>G c.8882T>G (p.Val2961Gly) n.653T>G c.7817T>G (p.Val2606Gly) | |
1 | g.214657330C>A | CA37381419 | CENPF | c.8706C>A (p.Val2902=) n.982C>A c.8883C>A (p.Val2961=) n.654C>A c.7818C>A (p.Val2606=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657330C= | CA2486377693 | CENPF | c.8706C= (p.Val2902=) n.982C= c.8883C= (p.Val2961=) n.654C= c.7818C= (p.Val2606=) | |
1 | g.214657330C>G | CA423429504 | CENPF | c.8706C>G (p.Val2902=) n.982C>G c.8883C>G (p.Val2961=) n.654C>G c.7818C>G (p.Val2606=) | |
1 | g.214657330C>T | CA423429500 | CENPF | c.8706C>T (p.Val2902=) n.982C>T c.8883C>T (p.Val2961=) n.654C>T c.7818C>T (p.Val2606=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657331A>C | CA344857520 | CENPF | c.8707A>C (p.Met2903Leu) n.983A>C c.8884A>C (p.Met2962Leu) n.655A>C c.7819A>C (p.Met2607Leu) | |
1 | g.214657331A>G | CA344857518 | CENPF | c.8707A>G (p.Met2903Val) n.983A>G c.8884A>G (p.Met2962Val) n.655A>G c.7819A>G (p.Met2607Val) | ClinVar |
1 | g.214657331A>T | CA344857517 | CENPF | c.8707A>T (p.Met2903Leu) n.983A>T c.8884A>T (p.Met2962Leu) n.655A>T c.7819A>T (p.Met2607Leu) | |
1 | g.214657332T>A | CA344857521 | CENPF | c.8708T>A (p.Met2903Lys) n.984T>A c.8885T>A (p.Met2962Lys) n.656T>A c.7820T>A (p.Met2607Lys) | |
1 | g.214657332T>C | CA344857522 | CENPF | c.8708T>C (p.Met2903Thr) n.984T>C c.8885T>C (p.Met2962Thr) n.656T>C c.7820T>C (p.Met2607Thr) | gnomAD v4 |
1 | g.214657332T>G | CA344857524 | CENPF | c.8708T>G (p.Met2903Arg) n.984T>G c.8885T>G (p.Met2962Arg) n.656T>G c.7820T>G (p.Met2607Arg) | |
1 | g.214657333G>A | CA344857526 | CENPF | c.8709G>A (p.Met2903Ile) n.985G>A c.8886G>A (p.Met2962Ile) n.657G>A c.7821G>A (p.Met2607Ile) | |
1 | g.214657333G>C | CA344857529 | CENPF | c.8709G>C (p.Met2903Ile) n.985G>C c.8886G>C (p.Met2962Ile) n.657G>C c.7821G>C (p.Met2607Ile) | |
1 | g.214657333G>T | CA344857530 | CENPF | c.8709G>T (p.Met2903Ile) n.985G>T c.8886G>T (p.Met2962Ile) n.657G>T c.7821G>T (p.Met2607Ile) | |
1 | g.214657334A>C | CA344857534 | CENPF | c.8710A>C (p.Ser2904Arg) n.986A>C c.8887A>C (p.Ser2963Arg) n.658A>C c.7822A>C (p.Ser2608Arg) | |
1 | g.214657334A>G | CA344857532 | CENPF | c.8710A>G (p.Ser2904Gly) n.986A>G c.8887A>G (p.Ser2963Gly) n.658A>G c.7822A>G (p.Ser2608Gly) | |
1 | g.214657334A>T | CA344857533 | CENPF | c.8710A>T (p.Ser2904Cys) n.986A>T c.8887A>T (p.Ser2963Cys) n.658A>T c.7822A>T (p.Ser2608Cys) | |
1 | g.214657335G>A | CA344857540 | CENPF | c.8711G>A (p.Ser2904Asn) n.987G>A c.8888G>A (p.Ser2963Asn) n.659G>A c.7823G>A (p.Ser2608Asn) | dbSNP |
1 | g.214657335G>C | CA344857542 | CENPF | c.8711G>C (p.Ser2904Thr) n.987G>C c.8888G>C (p.Ser2963Thr) n.659G>C c.7823G>C (p.Ser2608Thr) | |
1 | g.214657335G= | CA2486377694 | CENPF | c.8711G= (p.Ser2904=) n.987G= c.8888G= (p.Ser2963=) n.659G= c.7823G= (p.Ser2608=) | |
1 | g.214657335G>T | CA344857543 | CENPF | c.8711G>T (p.Ser2904Ile) n.987G>T c.8888G>T (p.Ser2963Ile) n.659G>T c.7823G>T (p.Ser2608Ile) | dbSNP |
1 | g.214657336T>A | CA344857545 | CENPF | c.8712T>A (p.Ser2904Arg) n.988T>A c.8889T>A (p.Ser2963Arg) n.660T>A c.7824T>A (p.Ser2608Arg) | |
1 | g.214657336T>C | CA423429515 | CENPF | c.8712T>C (p.Ser2904=) n.988T>C c.8889T>C (p.Ser2963=) n.660T>C c.7824T>C (p.Ser2608=) | dbSNP gnomAD v4 |
1 | g.214657336T>G | CA344857548 | CENPF | c.8712T>G (p.Ser2904Arg) n.988T>G c.8889T>G (p.Ser2963Arg) n.660T>G c.7824T>G (p.Ser2608Arg) | |
1 | g.214657336T= | CA2486377695 | CENPF | c.8712T= (p.Ser2904=) n.988T= c.8889T= (p.Ser2963=) n.660T= c.7824T= (p.Ser2608=) | |
1 | g.214657337G>A | CA344857550 | CENPF | c.8713G>A (p.Gly2905Ser) n.989G>A c.8890G>A (p.Gly2964Ser) n.661G>A c.7825G>A (p.Gly2609Ser) | |
1 | g.214657337G>C | CA344857552 | CENPF | c.8713G>C (p.Gly2905Arg) n.989G>C c.8890G>C (p.Gly2964Arg) n.661G>C c.7825G>C (p.Gly2609Arg) | |
1 | g.214657337G>T | CA344857551 | CENPF | c.8713G>T (p.Gly2905Cys) n.989G>T c.8890G>T (p.Gly2964Cys) n.661G>T c.7825G>T (p.Gly2609Cys) | |
1 | g.214657338G>A | CA344857554 | CENPF | c.8714G>A (p.Gly2905Asp) n.990G>A c.8891G>A (p.Gly2964Asp) n.662G>A c.7826G>A (p.Gly2609Asp) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657338G>C | CA344857556 | CENPF | c.8714G>C (p.Gly2905Ala) n.990G>C c.8891G>C (p.Gly2964Ala) n.662G>C c.7826G>C (p.Gly2609Ala) | |
1 | g.214657338G= | CA2486377696 | CENPF | c.8714G= (p.Gly2905=) n.990G= c.8891G= (p.Gly2964=) n.662G= c.7826G= (p.Gly2609=) | |
1 | g.214657338G>T | CA344857557 | CENPF | c.8714G>T (p.Gly2905Val) n.990G>T c.8891G>T (p.Gly2964Val) n.662G>T c.7826G>T (p.Gly2609Val) | |
1 | g.214657339T>A | CA423429523 | CENPF | c.8715T>A (p.Gly2905=) n.991T>A c.8892T>A (p.Gly2964=) n.663T>A c.7827T>A (p.Gly2609=) | |
1 | g.214657339T>C | CA423429522 | CENPF | c.8715T>C (p.Gly2905=) n.991T>C c.8892T>C (p.Gly2964=) n.663T>C c.7827T>C (p.Gly2609=) | ClinVar dbSNP gnomAD v4 |
1 | g.214657339T>G | CA423429521 | CENPF | c.8715T>G (p.Gly2905=) n.991T>G c.8892T>G (p.Gly2964=) n.663T>G c.7827T>G (p.Gly2609=) | gnomAD v4 |
1 | g.214657339T= | CA2486377697 | CENPF | c.8715T= (p.Gly2905=) n.991T= c.8892T= (p.Gly2964=) n.663T= c.7827T= (p.Gly2609=) | |
1 | g.214657339dup | CA2650488283 | CENPF | c.8715dup (p.Ile2906TyrfsTer11) n.991dup c.8892dup (p.Ile2965TyrfsTer11) n.663dup c.7827dup (p.Ile2610TyrfsTer11) | gnomAD v4 |
1 | g.214657340A= | CA2486377698 | CENPF | c.8716A= (p.Ile2906=) n.992A= c.8893A= (p.Ile2965=) n.664A= c.7828A= (p.Ile2610=) | |
1 | g.214657340A>C | CA344857558 | CENPF | c.8716A>C (p.Ile2906Leu) n.992A>C c.8893A>C (p.Ile2965Leu) n.664A>C c.7828A>C (p.Ile2610Leu) | |
1 | g.214657340A>G | CA344857559 | CENPF | c.8716A>G (p.Ile2906Val) n.992A>G c.8893A>G (p.Ile2965Val) n.664A>G c.7828A>G (p.Ile2610Val) | dbSNP |
1 | g.214657340A>T | CA344857560 | CENPF | c.8716A>T (p.Ile2906Phe) n.992A>T c.8893A>T (p.Ile2965Phe) n.664A>T c.7828A>T (p.Ile2610Phe) | |
1 | g.214657341T>A | CA344857562 | CENPF | c.8717T>A (p.Ile2906Asn) n.993T>A c.8894T>A (p.Ile2965Asn) n.665T>A c.7829T>A (p.Ile2610Asn) | |
1 | g.214657341T>C | CA344857563 | CENPF | c.8717T>C (p.Ile2906Thr) n.993T>C c.8894T>C (p.Ile2965Thr) n.665T>C c.7829T>C (p.Ile2610Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657341T>G | CA344857566 | CENPF | c.8717T>G (p.Ile2906Ser) n.993T>G c.8894T>G (p.Ile2965Ser) n.665T>G c.7829T>G (p.Ile2610Ser) | |
1 | g.214657341T= | CA2486377699 | CENPF | c.8717T= (p.Ile2906=) n.993T= c.8894T= (p.Ile2965=) n.665T= c.7829T= (p.Ile2610=) | |
1 | g.214657342T>A | CA423429525 | CENPF | c.8718T>A (p.Ile2906=) n.994T>A c.8895T>A (p.Ile2965=) n.666T>A c.7830T>A (p.Ile2610=) | |
1 | g.214657342T>C | CA423429526 | CENPF | c.8718T>C (p.Ile2906=) n.994T>C c.8895T>C (p.Ile2965=) n.666T>C c.7830T>C (p.Ile2610=) | gnomAD v4 |
1 | g.214657342T>G | CA344857568 | CENPF | c.8718T>G (p.Ile2906Met) n.994T>G c.8895T>G (p.Ile2965Met) n.666T>G c.7830T>G (p.Ile2610Met) | |
1 | g.214657343C>A | CA344857573 | CENPF | c.8719C>A (p.His2907Asn) n.995C>A c.8896C>A (p.His2966Asn) n.667C>A c.7831C>A (p.His2611Asn) | |
1 | g.214657343C>G | CA344857572 | CENPF | c.8719C>G (p.His2907Asp) n.995C>G c.8896C>G (p.His2966Asp) n.667C>G c.7831C>G (p.His2611Asp) | |
1 | g.214657343C>T | CA344857570 | CENPF | c.8719C>T (p.His2907Tyr) n.995C>T c.8896C>T (p.His2966Tyr) n.667C>T c.7831C>T (p.His2611Tyr) | |
1 | g.214657344A>C | CA344857575 | CENPF | c.8720A>C (p.His2907Pro) n.996A>C c.8897A>C (p.His2966Pro) n.668A>C c.7832A>C (p.His2611Pro) | |
1 | g.214657344A>G | CA344857582 | CENPF | c.8720A>G (p.His2907Arg) n.996A>G c.8897A>G (p.His2966Arg) n.668A>G c.7832A>G (p.His2611Arg) | |
1 | g.214657344A>T | CA344857580 | CENPF | c.8720A>T (p.His2907Leu) n.996A>T c.8897A>T (p.His2966Leu) n.668A>T c.7832A>T (p.His2611Leu) | |
1 | g.214657345C>A | CA344857586 | CENPF | c.8721C>A (p.His2907Gln) n.997C>A c.8898C>A (p.His2966Gln) n.669C>A c.7833C>A (p.His2611Gln) | |
1 | g.214657345C>G | CA344857588 | CENPF | c.8721C>G (p.His2907Gln) n.997C>G c.8898C>G (p.His2966Gln) n.669C>G c.7833C>G (p.His2611Gln) | |
1 | g.214657345C>T | CA423429530 | CENPF | c.8721C>T (p.His2907=) n.997C>T c.8898C>T (p.His2966=) n.669C>T c.7833C>T (p.His2611=) | gnomAD v4 |
1 | g.214657346C>A | CA344857592 | CENPF | c.8722C>A (p.Pro2908Thr) n.998C>A c.8899C>A (p.Pro2967Thr) n.670C>A c.7834C>A (p.Pro2612Thr) | gnomAD v4 |
1 | g.214657346C= | CA2486377700 | CENPF | c.8722C= (p.Pro2908=) n.998C= c.8899C= (p.Pro2967=) n.670C= c.7834C= (p.Pro2612=) | |
1 | g.214657346C>G | CA344857593 | CENPF | c.8722C>G (p.Pro2908Ala) n.998C>G c.8899C>G (p.Pro2967Ala) n.670C>G c.7834C>G (p.Pro2612Ala) | |
1 | g.214657346C>T | CA1391514 | CENPF | c.8722C>T (p.Pro2908Ser) n.998C>T c.8899C>T (p.Pro2967Ser) n.670C>T c.7834C>T (p.Pro2612Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.214657347C>A | CA344857596 | CENPF | c.8723C>A (p.Pro2908His) n.999C>A c.8900C>A (p.Pro2967His) n.671C>A c.7835C>A (p.Pro2612His) | |
1 | g.214657347C= | CA2486377701 | CENPF | c.8723C= (p.Pro2908=) n.999C= c.8900C= (p.Pro2967=) n.671C= c.7835C= (p.Pro2612=) | |
1 | g.214657347C>G | CA344857598 | CENPF | c.8723C>G (p.Pro2908Arg) n.999C>G c.8900C>G (p.Pro2967Arg) n.671C>G c.7835C>G (p.Pro2612Arg) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657347C>T | CA37381433 | CENPF | c.8723C>T (p.Pro2908Leu) n.999C>T c.8900C>T (p.Pro2967Leu) n.671C>T c.7835C>T (p.Pro2612Leu) | dbSNP |
1 | g.214657348T>A | CA423429537 | CENPF | c.8724T>A (p.Pro2908=) n.1000T>A c.8901T>A (p.Pro2967=) n.672T>A c.7836T>A (p.Pro2612=) | |
1 | g.214657348T>C | CA423429540 | CENPF | c.8724T>C (p.Pro2908=) n.1000T>C c.8901T>C (p.Pro2967=) n.672T>C c.7836T>C (p.Pro2612=) | |
1 | g.214657348T>G | CA423429541 | CENPF | c.8724T>G (p.Pro2908=) n.1000T>G c.8901T>G (p.Pro2967=) n.672T>G c.7836T>G (p.Pro2612=) | gnomAD v4 |
1 | g.214657349G>A | CA1391515 | CENPF | c.8725G>A (p.Ala2909Thr) n.1001G>A c.8902G>A (p.Ala2968Thr) n.673G>A c.7837G>A (p.Ala2613Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657349G>C | CA344857600 | CENPF | c.8725G>C (p.Ala2909Pro) n.1001G>C c.8902G>C (p.Ala2968Pro) n.673G>C c.7837G>C (p.Ala2613Pro) | |
1 | g.214657349G= | CA2486377702 | CENPF | c.8725G= (p.Ala2909=) n.1001G= c.8902G= (p.Ala2968=) n.673G= c.7837G= (p.Ala2613=) | |
1 | g.214657349G>T | CA344857602 | CENPF | c.8725G>T (p.Ala2909Ser) n.1001G>T c.8902G>T (p.Ala2968Ser) n.673G>T c.7837G>T (p.Ala2613Ser) | |
1 | g.214657350C>A | CA344857607 | CENPF | c.8726C>A (p.Ala2909Glu) n.1002C>A c.8903C>A (p.Ala2968Glu) n.674C>A c.7838C>A (p.Ala2613Glu) | |
1 | g.214657350C>G | CA344857605 | CENPF | c.8726C>G (p.Ala2909Gly) n.1002C>G c.8903C>G (p.Ala2968Gly) n.674C>G c.7838C>G (p.Ala2613Gly) | |
1 | g.214657350C>T | CA344857604 | CENPF | c.8726C>T (p.Ala2909Val) n.1002C>T c.8903C>T (p.Ala2968Val) n.674C>T c.7838C>T (p.Ala2613Val) | |
1 | g.214657351A>C | CA423429550 | CENPF | c.8727A>C (p.Ala2909=) n.1003A>C c.8904A>C (p.Ala2968=) n.675A>C c.7839A>C (p.Ala2613=) | gnomAD v4 |
1 | g.214657351A>G | CA423429551 | CENPF | c.8727A>G (p.Ala2909=) n.1003A>G c.8904A>G (p.Ala2968=) n.675A>G c.7839A>G (p.Ala2613=) | gnomAD v4 |
1 | g.214657351A>T | CA423429552 | CENPF | c.8727A>T (p.Ala2909=) n.1003A>T c.8904A>T (p.Ala2968=) n.675A>T c.7839A>T (p.Ala2613=) | |
1 | g.214657352G>A | CA344857609 | CENPF | c.8728G>A (p.Glu2910Lys) n.1004G>A c.8905G>A (p.Glu2969Lys) n.676G>A c.7840G>A (p.Glu2614Lys) | |
1 | g.214657352G>C | CA344857611 | CENPF | c.8728G>C (p.Glu2910Gln) n.1004G>C c.8905G>C (p.Glu2969Gln) n.676G>C c.7840G>C (p.Glu2614Gln) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.214657352G= | CA2486377703 | CENPF | c.8728G= (p.Glu2910=) n.1004G= c.8905G= (p.Glu2969=) n.676G= c.7840G= (p.Glu2614=) | |
1 | g.214657352G>T | CA344857612 | CENPF | c.8728G>T (p.Glu2910Ter) n.1004G>T c.8905G>T (p.Glu2969Ter) n.676G>T c.7840G>T (p.Glu2614Ter) | |
1 | g.214657353A= | CA1148560444 | CENPF | c.8729A= (p.Glu2910=) n.1005A= c.8906A= (p.Glu2969=) n.677A= c.7841A= (p.Glu2614=) | |
1 | g.214657353A>C | CA1391516 | CENPF | c.8729A>C (p.Glu2910Ala) n.1005A>C c.8906A>C (p.Glu2969Ala) n.677A>C c.7841A>C (p.Glu2614Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.214657353A>G | CA344857615 | CENPF | c.8729A>G (p.Glu2910Gly) n.1005A>G c.8906A>G (p.Glu2969Gly) n.677A>G c.7841A>G (p.Glu2614Gly) | |
1 | g.214657353A>T | CA344857616 | CENPF | c.8729A>T (p.Glu2910Val) n.1005A>T c.8906A>T (p.Glu2969Val) n.677A>T c.7841A>T (p.Glu2614Val) | |
1 | g.214657354A= | CA2486377704 | CENPF | c.8730A= (p.Glu2910=) n.1006A= c.8907A= (p.Glu2969=) n.678A= c.7842A= (p.Glu2614=) | |
1 | g.214657354A>C | CA344857619 | CENPF | c.8730A>C (p.Glu2910Asp) n.1006A>C c.8907A>C (p.Glu2969Asp) n.678A>C c.7842A>C (p.Glu2614Asp) | |
1 | g.214657354A>G | CA1391517 | CENPF | c.8730A>G (p.Glu2910=) n.1006A>G c.8907A>G (p.Glu2969=) n.678A>G c.7842A>G (p.Glu2614=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.214657354A>T | CA344857622 | CENPF | c.8730A>T (p.Glu2910Asp) n.1006A>T c.8907A>T (p.Glu2969Asp) n.678A>T c.7842A>T (p.Glu2614Asp) | |
1 | g.214657355G>A | CA344857623 | CENPF | c.8731G>A (p.Asp2911Asn) n.1007G>A c.8908G>A (p.Asp2970Asn) n.679G>A c.7843G>A (p.Asp2615Asn) | dbSNP |
1 | g.214657355G>C | CA344857624 | CENPF | c.8731G>C (p.Asp2911His) n.1007G>C c.8908G>C (p.Asp2970His) n.679G>C c.7843G>C (p.Asp2615His) | |
1 | g.214657355G= | CA2486377705 | CENPF | c.8731G= (p.Asp2911=) n.1007G= c.8908G= (p.Asp2970=) n.679G= c.7843G= (p.Asp2615=) | |
1 | g.214657355G>T | CA344857626 | CENPF | c.8731G>T (p.Asp2911Tyr) n.1007G>T c.8908G>T (p.Asp2970Tyr) n.679G>T c.7843G>T (p.Asp2615Tyr) | |
1 | g.214657356A>C | CA344857630 | CENPF | c.8732A>C (p.Asp2911Ala) n.1008A>C c.8909A>C (p.Asp2970Ala) n.680A>C c.7844A>C (p.Asp2615Ala) | |
1 | g.214657356A>G | CA344857629 | CENPF | c.8732A>G (p.Asp2911Gly) n.1008A>G c.8909A>G (p.Asp2970Gly) n.680A>G c.7844A>G (p.Asp2615Gly) | |
1 | g.214657356A>T | CA344857628 | CENPF | c.8732A>T (p.Asp2911Val) n.1008A>T c.8909A>T (p.Asp2970Val) n.680A>T c.7844A>T (p.Asp2615Val) | |
1 | g.214657357C>A | CA344857632 | CENPF | c.8733C>A (p.Asp2911Glu) n.1009C>A c.8910C>A (p.Asp2970Glu) n.681C>A c.7845C>A (p.Asp2615Glu) | |
1 | g.214657357C>G | CA344857631 | CENPF | c.8733C>G (p.Asp2911Glu) n.1009C>G c.8910C>G (p.Asp2970Glu) n.681C>G c.7845C>G (p.Asp2615Glu) | |
1 | g.214657357C>T | CA423429557 | CENPF | c.8733C>T (p.Asp2911=) n.1009C>T c.8910C>T (p.Asp2970=) n.681C>T c.7845C>T (p.Asp2615=) | |
1 | g.214657358A>C | CA344857633 | CENPF | c.8734A>C (p.Thr2912Pro) n.1010A>C c.8911A>C (p.Thr2971Pro) n.682A>C c.7846A>C (p.Thr2616Pro) | |
1 | g.214657358A>G | CA344857635 | CENPF | c.8734A>G (p.Thr2912Ala) n.1010A>G c.8911A>G (p.Thr2971Ala) n.682A>G c.7846A>G (p.Thr2616Ala) | |
1 | g.214657358A>T | CA344857636 | CENPF | c.8734A>T (p.Thr2912Ser) n.1010A>T c.8911A>T (p.Thr2971Ser) n.682A>T c.7846A>T (p.Thr2616Ser) | |
1 | g.214657359C>A | CA1391519 | CENPF | c.8735C>A (p.Thr2912Lys) n.1011C>A c.8912C>A (p.Thr2971Lys) n.683C>A c.7847C>A (p.Thr2616Lys) | dbSNP ExAC gnomAD v2 |
1 | g.214657359C= | CA2486377706 | CENPF | c.8735C= (p.Thr2912=) n.1011C= c.8912C= (p.Thr2971=) n.683C= c.7847C= (p.Thr2616=) | |
1 | g.214657359C>G | CA344857639 | CENPF | c.8735C>G (p.Thr2912Arg) n.1011C>G c.8912C>G (p.Thr2971Arg) n.683C>G c.7847C>G (p.Thr2616Arg) | |
1 | g.214657359C>T | CA1391518 | CENPF | c.8735C>T (p.Thr2912Met) n.1011C>T c.8912C>T (p.Thr2971Met) n.683C>T c.7847C>T (p.Thr2616Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.214657360G>A | CA1391520 | CENPF | c.8736G>A (p.Thr2912=) n.1012G>A c.8913G>A (p.Thr2971=) n.684G>A c.7848G>A (p.Thr2616=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.214657360G>C | CA423429565 | CENPF | c.8736G>C (p.Thr2912=) n.1012G>C c.8913G>C (p.Thr2971=) n.684G>C c.7848G>C (p.Thr2616=) | |
1 | g.214657360G= | CA1142280377 | CENPF | c.8736G= (p.Thr2912=) n.1012G= c.8913G= (p.Thr2971=) n.684G= c.7848G= (p.Thr2616=) | |
1 | g.214657360G>T | CA423429564 | CENPF | c.8736G>T (p.Thr2912=) n.1012G>T c.8913G>T (p.Thr2971=) n.684G>T c.7848G>T (p.Thr2616=) | dbSNP gnomAD v4 |
1 | g.214657361G>A | CA344857643 | CENPF | c.8737G>A (p.Glu2913Lys) n.1013G>A c.8914G>A (p.Glu2972Lys) n.685G>A c.7849G>A (p.Glu2617Lys) | |
1 | g.214657361G>C | CA344857644 | CENPF | c.8737G>C (p.Glu2913Gln) n.1013G>C c.8914G>C (p.Glu2972Gln) n.685G>C c.7849G>C (p.Glu2617Gln) | |
1 | g.214657361G>T | CA344857645 | CENPF | c.8737G>T (p.Glu2913Ter) n.1013G>T c.8914G>T (p.Glu2972Ter) n.685G>T c.7849G>T (p.Glu2617Ter) | |
1 | g.214657362A= | CA1143960473 | CENPF | c.8738A= (p.Glu2913=) n.1014A= c.8915A= (p.Glu2972=) n.686A= c.7850A= (p.Glu2617=) | |
1 | g.214657362A>C | CA344857646 | CENPF | c.8738A>C (p.Glu2913Ala) n.1014A>C c.8915A>C (p.Glu2972Ala) n.686A>C c.7850A>C (p.Glu2617Ala) | |
1 | g.214657362A>G | CA37381489 | CENPF | c.8738A>G (p.Glu2913Gly) n.1014A>G c.8915A>G (p.Glu2972Gly) n.686A>G c.7850A>G (p.Glu2617Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657362A>T | CA344857648 | CENPF | c.8738A>T (p.Glu2913Val) n.1014A>T c.8915A>T (p.Glu2972Val) n.686A>T c.7850A>T (p.Glu2617Val) | dbSNP |
1 | g.214657363A>C | CA344857650 | CENPF | c.8739A>C (p.Glu2913Asp) n.1015A>C c.8916A>C (p.Glu2972Asp) n.687A>C c.7851A>C (p.Glu2617Asp) | |
1 | g.214657363A>G | CA423429569 | CENPF | c.8739A>G (p.Glu2913=) n.1015A>G c.8916A>G (p.Glu2972=) n.687A>G c.7851A>G (p.Glu2617=) | gnomAD v4 |
1 | g.214657363A>T | CA344857653 | CENPF | c.8739A>T (p.Glu2913Asp) n.1015A>T c.8916A>T (p.Glu2972Asp) n.687A>T c.7851A>T (p.Glu2617Asp) | |
1 | g.214657364G>A | CA344857657 | CENPF | c.8740G>A (p.Gly2914Ser) n.1016G>A c.8917G>A (p.Gly2973Ser) n.688G>A c.7852G>A (p.Gly2618Ser) | |
1 | g.214657364G>C | CA344857664 | CENPF | c.8740G>C (p.Gly2914Arg) n.1016G>C c.8917G>C (p.Gly2973Arg) n.688G>C c.7852G>C (p.Gly2618Arg) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.214657364G= | CA2486377707 | CENPF | c.8740G= (p.Gly2914=) n.1016G= c.8917G= (p.Gly2973=) n.688G= c.7852G= (p.Gly2618=) | |
1 | g.214657364G>T | CA344857665 | CENPF | c.8740G>T (p.Gly2914Cys) n.1016G>T c.8917G>T (p.Gly2973Cys) n.688G>T c.7852G>T (p.Gly2618Cys) | gnomAD v4 |
1 | g.214657365G>A | CA344857666 | CENPF | c.8741G>A (p.Gly2914Asp) n.1017G>A c.8918G>A (p.Gly2973Asp) n.689G>A c.7853G>A (p.Gly2618Asp) | dbSNP gnomAD v2 |
1 | g.214657365G>C | CA344857668 | CENPF | c.8741G>C (p.Gly2914Ala) n.1017G>C c.8918G>C (p.Gly2973Ala) n.689G>C c.7853G>C (p.Gly2618Ala) | |
1 | g.214657365G= | CA2486377708 | CENPF | c.8741G= (p.Gly2914=) n.1017G= c.8918G= (p.Gly2973=) n.689G= c.7853G= (p.Gly2618=) | |
1 | g.214657365G>T | CA344857669 | CENPF | c.8741G>T (p.Gly2914Val) n.1017G>T c.8918G>T (p.Gly2973Val) n.689G>T c.7853G>T (p.Gly2618Val) | |
1 | g.214657366T>A | CA423429575 | CENPF | c.8742T>A (p.Gly2914=) n.1018T>A c.8919T>A (p.Gly2973=) n.690T>A c.7854T>A (p.Gly2618=) | |
1 | g.214657366T>C | CA423429576 | CENPF | c.8742T>C (p.Gly2914=) n.1018T>C c.8919T>C (p.Gly2973=) n.690T>C c.7854T>C (p.Gly2618=) | |
1 | g.214657366T>G | CA423429577 | CENPF | c.8742T>G (p.Gly2914=) n.1018T>G c.8919T>G (p.Gly2973=) n.690T>G c.7854T>G (p.Gly2618=) | |
1 | g.214657367A= | CA2486377709 | CENPF | c.8743A= (p.Thr2915=) n.1019A= c.8920A= (p.Thr2974=) n.691A= c.7855A= (p.Thr2619=) | |
1 | g.214657367A>C | CA344857671 | CENPF | c.8743A>C (p.Thr2915Pro) n.1019A>C c.8920A>C (p.Thr2974Pro) n.691A>C c.7855A>C (p.Thr2619Pro) | |
1 | g.214657367A>G | CA37381502 | CENPF | c.8743A>G (p.Thr2915Ala) n.1019A>G c.8920A>G (p.Thr2974Ala) n.691A>G c.7855A>G (p.Thr2619Ala) | dbSNP gnomAD v4 |
1 | g.214657367A>T | CA344857675 | CENPF | c.8743A>T (p.Thr2915Ser) n.1019A>T c.8920A>T (p.Thr2974Ser) n.691A>T c.7855A>T (p.Thr2619Ser) | |
1 | g.214657368C>A | CA344857677 | CENPF | c.8744C>A (p.Thr2915Asn) n.1020C>A c.8921C>A (p.Thr2974Asn) n.692C>A c.7856C>A (p.Thr2619Asn) | |
1 | g.214657368C>G | CA344857679 | CENPF | c.8744C>G (p.Thr2915Ser) n.1020C>G c.8921C>G (p.Thr2974Ser) n.692C>G c.7856C>G (p.Thr2619Ser) | |
1 | g.214657368C>T | CA344857681 | CENPF | c.8744C>T (p.Thr2915Ile) n.1020C>T c.8921C>T (p.Thr2974Ile) n.692C>T c.7856C>T (p.Thr2619Ile) | |
1 | g.214657369T>A | CA423429584 | CENPF | c.8745T>A (p.Thr2915=) n.1021T>A c.8922T>A (p.Thr2974=) n.693T>A c.7857T>A (p.Thr2619=) | |
1 | g.214657369T>C | CA423429586 | CENPF | c.8745T>C (p.Thr2915=) n.1021T>C c.8922T>C (p.Thr2974=) n.693T>C c.7857T>C (p.Thr2619=) | gnomAD v4 |
1 | g.214657369T>G | CA423429587 | CENPF | c.8745T>G (p.Thr2915=) n.1021T>G c.8922T>G (p.Thr2974=) n.693T>G c.7857T>G (p.Thr2619=) | |
1 | g.214657370G>A | CA344857683 | CENPF | c.8746G>A (p.Glu2916Lys) n.1022G>A c.8923G>A (p.Glu2975Lys) n.694G>A c.7858G>A (p.Glu2620Lys) | |
1 | g.214657370G>C | CA344857684 | CENPF | c.8746G>C (p.Glu2916Gln) n.1022G>C c.8923G>C (p.Glu2975Gln) n.694G>C c.7858G>C (p.Glu2620Gln) | |
1 | g.214657370G>T | CA344857682 | CENPF | c.8746G>T (p.Glu2916Ter) n.1022G>T c.8923G>T (p.Glu2975Ter) n.694G>T c.7858G>T (p.Glu2620Ter) | |
1 | g.214657371A>C | CA344857685 | CENPF | c.8747A>C (p.Glu2916Ala) n.1023A>C c.8924A>C (p.Glu2975Ala) n.695A>C c.7859A>C (p.Glu2620Ala) | |
1 | g.214657371A>G | CA344857689 | CENPF | c.8747A>G (p.Glu2916Gly) n.1023A>G c.8924A>G (p.Glu2975Gly) n.695A>G c.7859A>G (p.Glu2620Gly) | |
1 | g.214657371A>T | CA344857686 | CENPF | c.8747A>T (p.Glu2916Val) n.1023A>T c.8924A>T (p.Glu2975Val) n.695A>T c.7859A>T (p.Glu2620Val) | |
1 | g.214657372G>A | CA37381505 | CENPF | c.8748G>A (p.Glu2916=) n.1024G>A c.8925G>A (p.Glu2975=) n.696G>A c.7860G>A (p.Glu2620=) | dbSNP |
1 | g.214657372G>C | CA344857692 | CENPF | c.8748G>C (p.Glu2916Asp) n.1024G>C c.8925G>C (p.Glu2975Asp) n.696G>C c.7860G>C (p.Glu2620Asp) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657372G= | CA2486377710 | CENPF | c.8748G= (p.Glu2916=) n.1024G= c.8925G= (p.Glu2975=) n.696G= c.7860G= (p.Glu2620=) | |
1 | g.214657372G>T | CA344857695 | CENPF | c.8748G>T (p.Glu2916Asp) n.1024G>T c.8925G>T (p.Glu2975Asp) n.696G>T c.7860G>T (p.Glu2620Asp) | |
1 | g.214657373T>A | CA344857702 | CENPF | c.8749T>A (p.Phe2917Ile) n.1025T>A c.8926T>A (p.Phe2976Ile) n.697T>A c.7861T>A (p.Phe2621Ile) | |
1 | g.214657373T>C | CA344857703 | CENPF | c.8749T>C (p.Phe2917Leu) n.1025T>C c.8926T>C (p.Phe2976Leu) n.697T>C c.7861T>C (p.Phe2621Leu) | |
1 | g.214657373T>G | CA344857705 | CENPF | c.8749T>G (p.Phe2917Val) n.1025T>G c.8926T>G (p.Phe2976Val) n.697T>G c.7861T>G (p.Phe2621Val) | |
1 | g.214657374T>A | CA344857707 | CENPF | c.8750T>A (p.Phe2917Tyr) n.1026T>A c.8927T>A (p.Phe2976Tyr) n.698T>A c.7862T>A (p.Phe2621Tyr) | |
1 | g.214657374T>C | CA344857709 | CENPF | c.8750T>C (p.Phe2917Ser) n.1026T>C c.8927T>C (p.Phe2976Ser) n.698T>C c.7862T>C (p.Phe2621Ser) | dbSNP |
1 | g.214657374T>G | CA344857711 | CENPF | c.8750T>G (p.Phe2917Cys) n.1026T>G c.8927T>G (p.Phe2976Cys) n.698T>G c.7862T>G (p.Phe2621Cys) | |
1 | g.214657375T>A | CA344857712 | CENPF | c.8751T>A (p.Phe2917Leu) n.1027T>A c.8928T>A (p.Phe2976Leu) n.699T>A c.7863T>A (p.Phe2621Leu) | |
1 | g.214657375T>C | CA423429592 | CENPF | c.8751T>C (p.Phe2917=) n.1027T>C c.8928T>C (p.Phe2976=) n.699T>C c.7863T>C (p.Phe2621=) | |
1 | g.214657375T>G | CA344857713 | CENPF | c.8751T>G (p.Phe2917Leu) n.1027T>G c.8928T>G (p.Phe2976Leu) n.699T>G c.7863T>G (p.Phe2621Leu) | |
1 | g.214657376G>A | CA344857728 | CENPF | c.8752G>A (p.Glu2918Lys) n.1028G>A c.8929G>A (p.Glu2977Lys) n.700G>A c.7864G>A (p.Glu2622Lys) | gnomAD v4 |
1 | g.214657376G>C | CA344857726 | CENPF | c.8752G>C (p.Glu2918Gln) n.1028G>C c.8929G>C (p.Glu2977Gln) n.700G>C c.7864G>C (p.Glu2622Gln) | |
1 | g.214657376G>T | CA344857716 | CENPF | c.8752G>T (p.Glu2918Ter) n.1028G>T c.8929G>T (p.Glu2977Ter) n.700G>T c.7864G>T (p.Glu2622Ter) | |
1 | g.214657377A>C | CA344857730 | CENPF | c.8753A>C (p.Glu2918Ala) n.1029A>C c.8930A>C (p.Glu2977Ala) n.701A>C c.7865A>C (p.Glu2622Ala) | |
1 | g.214657377A>G | CA344857732 | CENPF | c.8753A>G (p.Glu2918Gly) n.1029A>G c.8930A>G (p.Glu2977Gly) n.701A>G c.7865A>G (p.Glu2622Gly) | gnomAD v4 |
1 | g.214657377A>T | CA344857734 | CENPF | c.8753A>T (p.Glu2918Val) n.1029A>T c.8930A>T (p.Glu2977Val) n.701A>T c.7865A>T (p.Glu2622Val) | |
1 | g.214657378G>A | CA423429599 | CENPF | c.8754G>A (p.Glu2918=) n.1030G>A c.8931G>A (p.Glu2977=) n.702G>A c.7866G>A (p.Glu2622=) | |
1 | g.214657378G>C | CA344857738 | CENPF | c.8754G>C (p.Glu2918Asp) n.1030G>C c.8931G>C (p.Glu2977Asp) n.702G>C c.7866G>C (p.Glu2622Asp) | |
1 | g.214657378G>T | CA344857744 | CENPF | c.8754G>T (p.Glu2918Asp) n.1030G>T c.8931G>T (p.Glu2977Asp) n.702G>T c.7866G>T (p.Glu2622Asp) | |
1 | g.214657379C>A | CA344857747 | CENPF | c.8755C>A (p.Pro2919Thr) n.1031C>A c.8932C>A (p.Pro2978Thr) n.703C>A c.7867C>A (p.Pro2623Thr) | gnomAD v4 |
1 | g.214657379C>G | CA344857751 | CENPF | c.8755C>G (p.Pro2919Ala) n.1031C>G c.8932C>G (p.Pro2978Ala) n.703C>G c.7867C>G (p.Pro2623Ala) | |
1 | g.214657379C>T | CA344857754 | CENPF | c.8755C>T (p.Pro2919Ser) n.1031C>T c.8932C>T (p.Pro2978Ser) n.703C>T c.7867C>T (p.Pro2623Ser) | |
1 | g.214657380C>A | CA344857759 | CENPF | c.8756C>A (p.Pro2919Gln) n.1032C>A c.8933C>A (p.Pro2978Gln) n.704C>A c.7868C>A (p.Pro2623Gln) | |
1 | g.214657380C>G | CA344857761 | CENPF | c.8756C>G (p.Pro2919Arg) n.1032C>G c.8933C>G (p.Pro2978Arg) n.704C>G c.7868C>G (p.Pro2623Arg) | |
1 | g.214657380C>T | CA344857763 | CENPF | c.8756C>T (p.Pro2919Leu) n.1032C>T c.8933C>T (p.Pro2978Leu) n.704C>T c.7868C>T (p.Pro2623Leu) | |
1 | g.214657381A= | CA2486377711 | CENPF | c.8757A= (p.Pro2919=) n.1033A= c.8934A= (p.Pro2978=) n.705A= c.7869A= (p.Pro2623=) | |
1 | g.214657381A>C | CA423429607 | CENPF | c.8757A>C (p.Pro2919=) n.1033A>C c.8934A>C (p.Pro2978=) n.705A>C c.7869A>C (p.Pro2623=) | |
1 | g.214657381A>G | CA423429613 | CENPF | c.8757A>G (p.Pro2919=) n.1033A>G c.8934A>G (p.Pro2978=) n.705A>G c.7869A>G (p.Pro2623=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657381A>T | CA423429616 | CENPF | c.8757A>T (p.Pro2919=) n.1033A>T c.8934A>T (p.Pro2978=) n.705A>T c.7869A>T (p.Pro2623=) | |
1 | g.214657382G>A | CA344857768 | CENPF | c.8758G>A (p.Glu2920Lys) n.1034G>A c.8935G>A (p.Glu2979Lys) n.706G>A c.7870G>A (p.Glu2624Lys) | |
1 | g.214657382G>C | CA344857770 | CENPF | c.8758G>C (p.Glu2920Gln) n.1034G>C c.8935G>C (p.Glu2979Gln) n.706G>C c.7870G>C (p.Glu2624Gln) | |
1 | g.214657382G>T | CA344857765 | CENPF | c.8758G>T (p.Glu2920Ter) n.1034G>T c.8935G>T (p.Glu2979Ter) n.706G>T c.7870G>T (p.Glu2624Ter) | |
1 | g.214657383A= | CA2486377712 | CENPF | c.8759A= (p.Glu2920=) n.1035A= c.8936A= (p.Glu2979=) n.707A= c.7871A= (p.Glu2624=) | |
1 | g.214657383A>C | CA344857771 | CENPF | c.8759A>C (p.Glu2920Ala) n.1035A>C c.8936A>C (p.Glu2979Ala) n.707A>C c.7871A>C (p.Glu2624Ala) | |
1 | g.214657383A>G | CA1391521 | CENPF | c.8759A>G (p.Glu2920Gly) n.1035A>G c.8936A>G (p.Glu2979Gly) n.707A>G c.7871A>G (p.Glu2624Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.214657383A>T | CA344857772 | CENPF | c.8759A>T (p.Glu2920Val) n.1035A>T c.8936A>T (p.Glu2979Val) n.707A>T c.7871A>T (p.Glu2624Val) | |
1 | g.214657384G>A | CA423429623 | CENPF | c.8760G>A (p.Glu2920=) n.1036G>A c.8937G>A (p.Glu2979=) n.708G>A c.7872G>A (p.Glu2624=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.214657384G>C | CA344857773 | CENPF | c.8760G>C (p.Glu2920Asp) n.1036G>C c.8937G>C (p.Glu2979Asp) n.708G>C c.7872G>C (p.Glu2624Asp) | gnomAD v4 |
1 | g.214657384G= | CA2486377713 | CENPF | c.8760G= (p.Glu2920=) n.1036G= c.8937G= (p.Glu2979=) n.708G= c.7872G= (p.Glu2624=) | |
1 | g.214657384G>T | CA344857774 | CENPF | c.8760G>T (p.Glu2920Asp) n.1036G>T c.8937G>T (p.Glu2979Asp) n.708G>T c.7872G>T (p.Glu2624Asp) | dbSNP gnomAD v2 |
1 | g.214657385G>A | CA344857780 | CENPF | c.8761G>A (p.Gly2921Arg) n.1037G>A c.8938G>A (p.Gly2980Arg) n.709G>A c.7873G>A (p.Gly2625Arg) | dbSNP |
1 | g.214657385G>C | CA344857778 | CENPF | c.8761G>C (p.Gly2921Arg) n.1037G>C c.8938G>C (p.Gly2980Arg) n.709G>C c.7873G>C (p.Gly2625Arg) | |
1 | g.214657385G= | CA2486377714 | CENPF | c.8761G= (p.Gly2921=) n.1037G= c.8938G= (p.Gly2980=) n.709G= c.7873G= (p.Gly2625=) | |
1 | g.214657385G>T | CA344857776 | CENPF | c.8761G>T (p.Gly2921Ter) n.1037G>T c.8938G>T (p.Gly2980Ter) n.709G>T c.7873G>T (p.Gly2625Ter) |