Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.63942847C>ACA400616352SCN4Ac.4267G>T (p.Val1423Phe)
17g.63942847C=CA2270161681SCN4Ac.4267G= (p.Val1423=)
17g.63942847C>GCA400616353SCN4Ac.4267G>C (p.Val1423Leu)
17g.63942847C>TCA292958144SCN4Ac.4267G>A (p.Val1423Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63942848C>ACA501214802SCN4Ac.4266G>T (p.Val1422=)
17g.63942848C=CA2270161682SCN4Ac.4266G= (p.Val1422=)
17g.63942848C>GCA501214804SCN4Ac.4266G>C (p.Val1422=)
17g.63942848C>TCA501214806SCN4Ac.4266G>A (p.Val1422=)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63942849A>CCA400616354SCN4Ac.4265T>G (p.Val1422Gly)
ClinVar
17g.63942849A>GCA400616355SCN4Ac.4265T>C (p.Val1422Ala)
17g.63942849A>TCA400616356SCN4Ac.4265T>A (p.Val1422Glu)
17g.63942850C>ACA400616357SCN4Ac.4264G>T (p.Val1422Leu)
17g.63942850C=CA2270161683SCN4Ac.4264G= (p.Val1422=)
17g.63942850C>GCA400616358SCN4Ac.4264G>C (p.Val1422Leu)
17g.63942850C>TCA8709028SCN4Ac.4264G>A (p.Val1422Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.63942851G>ACA8709029SCN4Ac.4263C>T (p.Phe1421=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.63942851G>CCA400616359SCN4Ac.4263C>G (p.Phe1421Leu)
dbSNP
17g.63942851G=CA2270161684SCN4Ac.4263C= (p.Phe1421=)
17g.63942851G>TCA400616360SCN4Ac.4263C>A (p.Phe1421Leu)
17g.63942852A>CCA400616362SCN4Ac.4262T>G (p.Phe1421Cys)
17g.63942852A>GCA400616363SCN4Ac.4262T>C (p.Phe1421Ser)
17g.63942852A>TCA400616361SCN4Ac.4262T>A (p.Phe1421Tyr)
17g.63942853A>CCA400616365SCN4Ac.4261T>G (p.Phe1421Val)
17g.63942853A>GCA400616364SCN4Ac.4261T>C (p.Phe1421Leu)
gnomAD v4
17g.63942853A>TCA400616366SCN4Ac.4261T>A (p.Phe1421Ile)
17g.63942854G>ACA501214809SCN4Ac.4260C>T (p.Asp1420=)
ClinVar dbSNP gnomAD v4
17g.63942854G>CCA400616367SCN4Ac.4260C>G (p.Asp1420Glu)
17g.63942854G=CA2270161685SCN4Ac.4260C= (p.Asp1420=)
17g.63942854G>TCA400616368SCN4Ac.4260C>A (p.Asp1420Glu)
17g.63942855T>ACA400616369SCN4Ac.4259A>T (p.Asp1420Val)
17g.63942855T>CCA400616370SCN4Ac.4259A>G (p.Asp1420Gly)
gnomAD v4
17g.63942855T>GCA400616371SCN4Ac.4259A>C (p.Asp1420Ala)
17g.63942856C>ACA400616372SCN4Ac.4258G>T (p.Asp1420Tyr)
dbSNP
17g.63942856C=CA2270161686SCN4Ac.4258G= (p.Asp1420=)
17g.63942856C>GCA400616373SCN4Ac.4258G>C (p.Asp1420His)
17g.63942856C>TCA400616374SCN4Ac.4258G>A (p.Asp1420Asn)
ClinVar dbSNP
17g.63942857A>CCA400616375SCN4Ac.4257T>G (p.Phe1419Leu)
17g.63942857A>GCA501214810SCN4Ac.4257T>C (p.Phe1419=)
17g.63942857A>TCA400616376SCN4Ac.4257T>A (p.Phe1419Leu)
17g.63942858A>CCA400616379SCN4Ac.4256T>G (p.Phe1419Cys)
17g.63942858A>GCA400616378SCN4Ac.4256T>C (p.Phe1419Ser)
17g.63942858A>TCA400616377SCN4Ac.4256T>A (p.Phe1419Tyr)
17g.63942859A>CCA400616380SCN4Ac.4255T>G (p.Phe1419Val)
17g.63942859A>GCA400616381SCN4Ac.4255T>C (p.Phe1419Leu)
17g.63942859A>TCA400616382SCN4Ac.4255T>A (p.Phe1419Ile)
17g.63942860G>ACA501214811SCN4Ac.4254C>T (p.Ile1418=)
dbSNP gnomAD v4
17g.63942860G>CCA400616383SCN4Ac.4254C>G (p.Ile1418Met)
17g.63942860G>TCA501214812SCN4Ac.4254C>A (p.Ile1418=)
17g.63942861A>CCA400616384SCN4Ac.4253T>G (p.Ile1418Ser)
17g.63942861A>GCA400616385SCN4Ac.4253T>C (p.Ile1418Thr)
17g.63942861A>TCA400616386SCN4Ac.4253T>A (p.Ile1418Asn)
17g.63942862T>ACA400616387SCN4Ac.4252A>T (p.Ile1418Phe)
17g.63942862T>CCA400616388SCN4Ac.4252A>G (p.Ile1418Val)
dbSNP gnomAD v4
17g.63942862T>GCA400616389SCN4Ac.4252A>C (p.Ile1418Leu)
17g.63942862T=CA2270161687SCN4Ac.4252A= (p.Ile1418=)
17g.63942863G>ACA501214813SCN4Ac.4251C>T (p.Asn1417=)
17g.63942863G>CCA400616390SCN4Ac.4251C>G (p.Asn1417Lys)
17g.63942863G>TCA400616391SCN4Ac.4251C>A (p.Asn1417Lys)
17g.63942864T>ACA400616393SCN4Ac.4250A>T (p.Asn1417Ile)
17g.63942864T>CCA400616394SCN4Ac.4250A>G (p.Asn1417Ser)
17g.63942864T>GCA400616392SCN4Ac.4250A>C (p.Asn1417Thr)
17g.63942865T>ACA400616395SCN4Ac.4249A>T (p.Asn1417Tyr)
17g.63942865T>CCA400616396SCN4Ac.4249A>G (p.Asn1417Asp)
17g.63942865T>GCA400616397SCN4Ac.4249A>C (p.Asn1417His)
17g.63942866C>ACA400616398SCN4Ac.4248G>T (p.Trp1416Cys)
17g.63942866C=CA2270161688SCN4Ac.4248G= (p.Trp1416=)
17g.63942866C>GCA400616399SCN4Ac.4248G>C (p.Trp1416Cys)
17g.63942866C>TCA400616400SCN4Ac.4248G>A (p.Trp1416Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.63942867C>ACA400616401SCN4Ac.4247G>T (p.Trp1416Leu)
17g.63942867C>GCA400616402SCN4Ac.4247G>C (p.Trp1416Ser)
17g.63942867C>TCA400616403SCN4Ac.4247G>A (p.Trp1416Ter)
17g.63942868A>CCA400616404SCN4Ac.4246T>G (p.Trp1416Gly)
17g.63942868A>GCA400616405SCN4Ac.4246T>C (p.Trp1416Arg)
17g.63942868A>TCA400616406SCN4Ac.4246T>A (p.Trp1416Arg)
17g.63942869G>ACA501214814SCN4Ac.4245C>T (p.Gly1415=)
17g.63942869G>CCA501214815SCN4Ac.4245C>G (p.Gly1415=)
17g.63942869G>TCA501214816SCN4Ac.4245C>A (p.Gly1415=)
17g.63942870C>ACA400616409SCN4Ac.4244G>T (p.Gly1415Val)
17g.63942870C>GCA400616407SCN4Ac.4244G>C (p.Gly1415Ala)
17g.63942870C>TCA400616408SCN4Ac.4244G>A (p.Gly1415Asp)
17g.63942871C>ACA400616410SCN4Ac.4243G>T (p.Gly1415Cys)
17g.63942871C>GCA400616411SCN4Ac.4243G>C (p.Gly1415Arg)
17g.63942871C>TCA400616412SCN4Ac.4243G>A (p.Gly1415Ser)
gnomAD v4
17g.63942872A>CCA501214817SCN4Ac.4242T>G (p.Val1414=)
gnomAD v4
17g.63942872A>GCA501214818SCN4Ac.4242T>C (p.Val1414=)
17g.63942872A>TCA501214819SCN4Ac.4242T>A (p.Val1414=)
17g.63942873A=CA2270161689SCN4Ac.4241T= (p.Val1414=)
17g.63942873A>CCA400616413SCN4Ac.4241T>G (p.Val1414Gly)
17g.63942873A>GCA400616414SCN4Ac.4241T>C (p.Val1414Ala)
dbSNP gnomAD v2 gnomAD v4
17g.63942873A>TCA400616415SCN4Ac.4241T>A (p.Val1414Asp)
17g.63942874C>ACA400616416SCN4Ac.4240G>T (p.Val1414Phe)
17g.63942874C=CA2270161690SCN4Ac.4240G= (p.Val1414=)
17g.63942874C>GCA400616417SCN4Ac.4240G>C (p.Val1414Leu)
17g.63942874C>TCA8709030SCN4Ac.4240G>A (p.Val1414Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.63942875G>ACA8709031SCN4Ac.4239C>T (p.Thr1413=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942875G>CCA501214820SCN4Ac.4239C>G (p.Thr1413=)
17g.63942875G=CA2270161691SCN4Ac.4239C= (p.Thr1413=)
17g.63942875G>TCA501214821SCN4Ac.4239C>A (p.Thr1413=)
17g.63942876G>ACA400616418SCN4Ac.4238C>T (p.Thr1413Ile)
ClinVar dbSNP gnomAD v4
17g.63942876G>CCA400616419SCN4Ac.4238C>G (p.Thr1413Ser)
17g.63942876G=CA2270161692SCN4Ac.4238C= (p.Thr1413=)
17g.63942876G>TCA400616420SCN4Ac.4238C>A (p.Thr1413Asn)
17g.63942877T>ACA400616422SCN4Ac.4237A>T (p.Thr1413Ser)
17g.63942877T>CCA400616423SCN4Ac.4237A>G (p.Thr1413Ala)
17g.63942877T>GCA400616421SCN4Ac.4237A>C (p.Thr1413Pro)
17g.63942878G>ACA501214822SCN4Ac.4236C>T (p.Phe1412=)
17g.63942878G>CCA400616424SCN4Ac.4236C>G (p.Phe1412Leu)
17g.63942878G=CA2270161693SCN4Ac.4236C= (p.Phe1412=)
17g.63942878G>TCA8709032SCN4Ac.4236C>A (p.Phe1412Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942879A>CCA400616425SCN4Ac.4235T>G (p.Phe1412Cys)
17g.63942879A>GCA400616426SCN4Ac.4235T>C (p.Phe1412Ser)
17g.63942879A>TCA400616427SCN4Ac.4235T>A (p.Phe1412Tyr)
17g.63942880A>CCA400616428SCN4Ac.4234T>G (p.Phe1412Val)
17g.63942880A>GCA400616429SCN4Ac.4234T>C (p.Phe1412Leu)
ClinVar
17g.63942880A>TCA400616430SCN4Ac.4234T>A (p.Phe1412Ile)
17g.63942881G>ACA501214823SCN4Ac.4233C>T (p.Tyr1411=)
17g.63942881G>CCA400616431SCN4Ac.4233C>G (p.Tyr1411Ter)
17g.63942881G>TCA400616432SCN4Ac.4233C>A (p.Tyr1411Ter)
17g.63942882T>ACA400616433SCN4Ac.4232A>T (p.Tyr1411Phe)
17g.63942882T>CCA400616434SCN4Ac.4232A>G (p.Tyr1411Cys)
gnomAD v4
17g.63942882T>GCA400616435SCN4Ac.4232A>C (p.Tyr1411Ser)
17g.63942883A=CA2270161694SCN4Ac.4231T= (p.Tyr1411=)
17g.63942883A>CCA400616438SCN4Ac.4231T>G (p.Tyr1411Asp)
17g.63942883A>GCA400616437SCN4Ac.4231T>C (p.Tyr1411His)
17g.63942883A>TCA400616436SCN4Ac.4231T>A (p.Tyr1411Asn)
dbSNP
17g.63942884G>ACA8709033SCN4Ac.4230C>T (p.Tyr1410=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942884G>CCA400616439SCN4Ac.4230C>G (p.Tyr1410Ter)
17g.63942884G=CA2270161695SCN4Ac.4230C= (p.Tyr1410=)
17g.63942884G>TCA400616440SCN4Ac.4230C>A (p.Tyr1410Ter)
17g.63942885T>ACA400616441SCN4Ac.4229A>T (p.Tyr1410Phe)
17g.63942885T>CCA400616442SCN4Ac.4229A>G (p.Tyr1410Cys)
ClinVar dbSNP gnomAD v4
17g.63942885T>GCA400616443SCN4Ac.4229A>C (p.Tyr1410Ser)
17g.63942886A>CCA400616444SCN4Ac.4228T>G (p.Tyr1410Asp)
17g.63942886A>GCA400616445SCN4Ac.4228T>C (p.Tyr1410His)
17g.63942886A>TCA400616446SCN4Ac.4228T>A (p.Tyr1410Asn)
17g.63942887C>ACA400616447SCN4Ac.4227G>T (p.Gln1409His)
17g.63942887C>GCA400616448SCN4Ac.4227G>C (p.Gln1409His)
17g.63942887C>TCA501214824SCN4Ac.4227G>A (p.Gln1409=)
17g.63942888T>ACA400616449SCN4Ac.4226A>T (p.Gln1409Leu)
17g.63942888T>CCA400616450SCN4Ac.4226A>G (p.Gln1409Arg)
17g.63942888T>GCA400616451SCN4Ac.4226A>C (p.Gln1409Pro)
17g.63942889G>ACA400616453SCN4Ac.4225C>T (p.Gln1409Ter)
17g.63942889G>CCA400616454SCN4Ac.4225C>G (p.Gln1409Glu)
17g.63942889G>TCA400616452SCN4Ac.4225C>A (p.Gln1409Lys)
17g.63942890G>ACA501214825SCN4Ac.4224C>T (p.Arg1408=)
17g.63942890G>CCA501214827SCN4Ac.4224C>G (p.Arg1408=)
17g.63942890G>TCA501214826SCN4Ac.4224C>A (p.Arg1408=)
17g.63942891C>ACA400616455SCN4Ac.4223G>T (p.Arg1408Leu)
17g.63942891C=CA2270161696SCN4Ac.4223G= (p.Arg1408=)
17g.63942891C>GCA400616456SCN4Ac.4223G>C (p.Arg1408Pro)
17g.63942891C>TCA400616457SCN4Ac.4223G>A (p.Arg1408His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.63942892G>ACA8709034SCN4Ac.4222C>T (p.Arg1408Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942892G>CCA400616458SCN4Ac.4222C>G (p.Arg1408Gly)
gnomAD v4
17g.63942892G=CA2270161697SCN4Ac.4222C= (p.Arg1408=)
17g.63942892G>TCA8709035SCN4Ac.4222C>A (p.Arg1408Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942893C>ACA501214828SCN4Ac.4221G>T (p.Leu1407=)
17g.63942893C>GCA501214829SCN4Ac.4221G>C (p.Leu1407=)
17g.63942893C>TCA501214830SCN4Ac.4221G>A (p.Leu1407=)
gnomAD v4
17g.63942894A>CCA400616459SCN4Ac.4220T>G (p.Leu1407Arg)
gnomAD v4
17g.63942894A>GCA400616460SCN4Ac.4220T>C (p.Leu1407Pro)
17g.63942894A>TCA400616461SCN4Ac.4220T>A (p.Leu1407Gln)
17g.63942895G>ACA501214831SCN4Ac.4219C>T (p.Leu1407=)
17g.63942895G>CCA400616462SCN4Ac.4219C>G (p.Leu1407Val)
17g.63942895G>TCA400616463SCN4Ac.4219C>A (p.Leu1407Met)
17g.63942896G>ACA501214832SCN4Ac.4218C>T (p.Ala1406=)
17g.63942896G>CCA8709036SCN4Ac.4218C>G (p.Ala1406=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942896G=CA2270161698SCN4Ac.4218C= (p.Ala1406=)
17g.63942896G>TCA501214833SCN4Ac.4218C>A (p.Ala1406=)
17g.63942897G>ACA400616465SCN4Ac.4217C>T (p.Ala1406Val)
17g.63942897G>CCA400616466SCN4Ac.4217C>G (p.Ala1406Gly)
17g.63942897G>TCA400616464SCN4Ac.4217C>A (p.Ala1406Asp)
17g.63942898C>ACA400616467SCN4Ac.4216G>T (p.Ala1406Ser)
gnomAD v4
17g.63942898C=CA2270161699SCN4Ac.4216G= (p.Ala1406=)
17g.63942898C>GCA400616468SCN4Ac.4216G>C (p.Ala1406Pro)
17g.63942898C>TCA8709037SCN4Ac.4216G>A (p.Ala1406Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942899G>ACA8709038SCN4Ac.4215C>T (p.Leu1405=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942899G>CCA501214834SCN4Ac.4215C>G (p.Leu1405=)
17g.63942899G=CA2270161700SCN4Ac.4215C= (p.Leu1405=)
17g.63942899G>TCA501214835SCN4Ac.4215C>A (p.Leu1405=)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63942900A>CCA400616471SCN4Ac.4214T>G (p.Leu1405Arg)
17g.63942900A>GCA400616470SCN4Ac.4214T>C (p.Leu1405Pro)
17g.63942900A>TCA400616469SCN4Ac.4214T>A (p.Leu1405His)
17g.63942901G>ACA400616472SCN4Ac.4213C>T (p.Leu1405Phe)
17g.63942901G>CCA400616473SCN4Ac.4213C>G (p.Leu1405Val)
17g.63942901G>TCA400616474SCN4Ac.4213C>A (p.Leu1405Ile)
gnomAD v4
17g.63942902C>ACA400616475SCN4Ac.4212G>T (p.Met1404Ile)
17g.63942902C>GCA400616476SCN4Ac.4212G>C (p.Met1404Ile)
17g.63942902C>TCA400616477SCN4Ac.4212G>A (p.Met1404Ile)
COSMIC
17g.63942903A>CCA400616480SCN4Ac.4211T>G (p.Met1404Arg)
17g.63942903A>GCA400616479SCN4Ac.4211T>C (p.Met1404Thr)
17g.63942903A>TCA400616478SCN4Ac.4211T>A (p.Met1404Lys)
17g.63942904T>ACA400616481SCN4Ac.4210A>T (p.Met1404Leu)
17g.63942904T>CCA8709039SCN4Ac.4210A>G (p.Met1404Val)
dbSNP ExAC gnomAD v3 gnomAD v4
17g.63942904T>GCA400616482SCN4Ac.4210A>C (p.Met1404Leu)
17g.63942904T=CA2270161701SCN4Ac.4210A= (p.Met1404=)
17g.63942905C>ACA400616483SCN4Ac.4209G>T (p.Lys1403Asn)
17g.63942905C>GCA400616484SCN4Ac.4209G>C (p.Lys1403Asn)
ClinVar dbSNP
17g.63942905C>TCA501214836SCN4Ac.4209G>A (p.Lys1403=)
COSMIC
17g.63942906T>ACA400616485SCN4Ac.4208A>T (p.Lys1403Met)
dbSNP
17g.63942906T>CCA400616486SCN4Ac.4208A>G (p.Lys1403Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.63942906T>GCA400616487SCN4Ac.4208A>C (p.Lys1403Thr)
17g.63942906T=CA2270161702SCN4Ac.4208A= (p.Lys1403=)
17g.63942907T>ACA400616488SCN4Ac.4207A>T (p.Lys1403Ter)
dbSNP
17g.63942907T>CCA400616489SCN4Ac.4207A>G (p.Lys1403Glu)
17g.63942907T>GCA400616490SCN4Ac.4207A>C (p.Lys1403Gln)
ClinVar dbSNP
17g.63942907T=CA2270161703SCN4Ac.4207A= (p.Lys1403=)
17g.63942908G>ACA501214837SCN4Ac.4206C>T (p.Leu1402=)
17g.63942908G>CCA501214838SCN4Ac.4206C>G (p.Leu1402=)
dbSNP gnomAD v4
17g.63942908G=CA2270161704SCN4Ac.4206C= (p.Leu1402=)
17g.63942908G>TCA501214839SCN4Ac.4206C>A (p.Leu1402=)
17g.63942909A>CCA400616491SCN4Ac.4205T>G (p.Leu1402Arg)
17g.63942909A>GCA400616492SCN4Ac.4205T>C (p.Leu1402Pro)
17g.63942909A>TCA400616493SCN4Ac.4205T>A (p.Leu1402His)
17g.63942910G>ACA400616494SCN4Ac.4204C>T (p.Leu1402Phe)
17g.63942910G>CCA400616495SCN4Ac.4204C>G (p.Leu1402Val)
17g.63942910G>TCA400616496SCN4Ac.4204C>A (p.Leu1402Ile)
17g.63942911C>ACA501214840SCN4Ac.4203G>T (p.Val1401=)
17g.63942911C>GCA501214841SCN4Ac.4203G>C (p.Val1401=)
17g.63942911C>TCA501214842SCN4Ac.4203G>A (p.Val1401=)
gnomAD v4
17g.63942912A>CCA400616499SCN4Ac.4202T>G (p.Val1401Gly)
17g.63942912A>GCA400616497SCN4Ac.4202T>C (p.Val1401Ala)
17g.63942912A>TCA400616498SCN4Ac.4202T>A (p.Val1401Glu)
17g.63942913C>ACA400616500SCN4Ac.4201G>T (p.Val1401Leu)
17g.63942913C=CA2270161705SCN4Ac.4201G= (p.Val1401=)
17g.63942913C>GCA400616501SCN4Ac.4201G>C (p.Val1401Leu)
17g.63942913C>TCA8709040SCN4Ac.4201G>A (p.Val1401Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.63942914G>ACA8709041SCN4Ac.4200C>T (p.Cys1400=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.63942914G>CCA400616502SCN4Ac.4200C>G (p.Cys1400Trp)
17g.63942914G=CA2270161706SCN4Ac.4200C= (p.Cys1400=)
17g.63942914G>TCA400616503SCN4Ac.4200C>A (p.Cys1400Ter)
dbSNP
17g.63942915C>ACA400616504SCN4Ac.4199G>T (p.Cys1400Phe)
gnomAD v4
17g.63942915C>GCA400616505SCN4Ac.4199G>C (p.Cys1400Ser)
17g.63942915C>TCA400616506SCN4Ac.4199G>A (p.Cys1400Tyr)
17g.63942916A>CCA400616507SCN4Ac.4198T>G (p.Cys1400Gly)
17g.63942916A>GCA400616508SCN4Ac.4198T>C (p.Cys1400Arg)
gnomAD v4
17g.63942916A>TCA400616509SCN4Ac.4198T>A (p.Cys1400Ser)
ClinVar dbSNP
17g.63942917C>ACA400616510SCN4Ac.4197G>T (p.Glu1399Asp)
17g.63942917C>GCA400616511SCN4Ac.4197G>C (p.Glu1399Asp)
17g.63942917C>TCA501214843SCN4Ac.4197G>A (p.Glu1399=)
17g.63942918T>ACA400616512SCN4Ac.4196A>T (p.Glu1399Val)
17g.63942918T>CCA400616513SCN4Ac.4196A>G (p.Glu1399Gly)
17g.63942918T>GCA400616514SCN4Ac.4196A>C (p.Glu1399Ala)
17g.63942919C>ACA400616515SCN4Ac.4195G>T (p.Glu1399Ter)
dbSNP
17g.63942919C=CA2270161707SCN4Ac.4195G= (p.Glu1399=)
17g.63942919C>GCA400616516SCN4Ac.4195G>C (p.Glu1399Gln)
17g.63942919C>TCA400616517SCN4Ac.4195G>A (p.Glu1399Lys)
17g.63942920C>ACA501214846SCN4Ac.4194G>T (p.Gly1398=)
17g.63942920C>GCA501214845SCN4Ac.4194G>C (p.Gly1398=)
17g.63942920C>TCA501214844SCN4Ac.4194G>A (p.Gly1398=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.63942921C>ACA400616518SCN4Ac.4193G>T (p.Gly1398Val)
17g.63942921C>GCA400616519SCN4Ac.4193G>C (p.Gly1398Ala)
17g.63942921C>TCA400616520SCN4Ac.4193G>A (p.Gly1398Glu)
COSMIC
17g.63942922C>ACA400616521SCN4Ac.4192G>T (p.Gly1398Trp)
gnomAD v4
17g.63942922C>GCA400616522SCN4Ac.4192G>C (p.Gly1398Arg)
17g.63942922C>TCA400616523SCN4Ac.4192G>A (p.Gly1398Arg)
COSMIC
17g.63942923T>ACA501214847SCN4Ac.4191A>T (p.Thr1397=)
17g.63942923T>CCA501214848SCN4Ac.4191A>G (p.Thr1397=)
17g.63942923T>GCA501214849SCN4Ac.4191A>C (p.Thr1397=)
17g.63942924G>ACA400616526SCN4Ac.4190C>T (p.Thr1397Ile)
gnomAD v4
17g.63942924G>CCA400616524SCN4Ac.4190C>G (p.Thr1397Arg)
17g.63942924G>TCA400616525SCN4Ac.4190C>A (p.Thr1397Lys)
17g.63942925T>ACA400616527SCN4Ac.4189A>T (p.Thr1397Ser)
17g.63942925T>CCA400616528SCN4Ac.4189A>G (p.Thr1397Ala)
17g.63942925T>GCA400616529SCN4Ac.4189A>C (p.Thr1397Pro)
17g.63942926G>ACA501214850SCN4Ac.4188C>T (p.Phe1396=)
17g.63942926G>CCA400616530SCN4Ac.4188C>G (p.Phe1396Leu)
17g.63942926G>TCA400616531SCN4Ac.4188C>A (p.Phe1396Leu)
17g.63942927A>CCA400616532SCN4Ac.4187T>G (p.Phe1396Cys)
17g.63942927A>GCA400616533SCN4Ac.4187T>C (p.Phe1396Ser)
17g.63942927A>TCA400616534SCN4Ac.4187T>A (p.Phe1396Tyr)
17g.63942928A>CCA400616535SCN4Ac.4186T>G (p.Phe1396Val)
17g.63942928A>GCA400616536SCN4Ac.4186T>C (p.Phe1396Leu)
17g.63942928A>TCA400616537SCN4Ac.4186T>A (p.Phe1396Ile)
17g.63942929G>ACA501214851SCN4Ac.4185C>T (p.Ile1395=)
COSMIC
17g.63942929G>CCA400616538SCN4Ac.4185C>G (p.Ile1395Met)
17g.63942929G>TCA501214852SCN4Ac.4185C>A (p.Ile1395=)
17g.63942937_63942939delCA2639308428SCN4Ac.4183_4185del (p.Ile1395del)
gnomAD v4
17g.63942930A>CCA400616541SCN4Ac.4184T>G (p.Ile1395Ser)
17g.63942930A>GCA400616540SCN4Ac.4184T>C (p.Ile1395Thr)
17g.63942930A>TCA400616539SCN4Ac.4184T>A (p.Ile1395Asn)
17g.63942931T>ACA400616543SCN4Ac.4183A>T (p.Ile1395Phe)
gnomAD v4
17g.63942931T>CCA400616542SCN4Ac.4183A>G (p.Ile1395Val)
ClinVar dbSNP gnomAD v4
17g.63942931T>GCA400616544SCN4Ac.4183A>C (p.Ile1395Leu)
17g.63942931T=CA2270161708SCN4Ac.4183A= (p.Ile1395=)
17g.63942932G>ACA501214853SCN4Ac.4182C>T (p.Ile1394=)
17g.63942932G>CCA400616545SCN4Ac.4182C>G (p.Ile1394Met)
17g.63942932G>TCA501214854SCN4Ac.4182C>A (p.Ile1394=)
17g.63942933A=CA2270161709SCN4Ac.4181T= (p.Ile1394=)
17g.63942933A>CCA400616546SCN4Ac.4181T>G (p.Ile1394Ser)
17g.63942933A>GCA400616547SCN4Ac.4181T>C (p.Ile1394Thr)
17g.63942933A>TCA8709042SCN4Ac.4181T>A (p.Ile1394Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.63942934T>ACA400616548SCN4Ac.4180A>T (p.Ile1394Phe)
17g.63942934T>CCA292958193SCN4Ac.4180A>G (p.Ile1394Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.63942934T>GCA400616549SCN4Ac.4180A>C (p.Ile1394Leu)
17g.63942934T=CA2270161710SCN4Ac.4180A= (p.Ile1394=)
17g.63942935G>ACA501214855SCN4Ac.4179C>T (p.Ile1393=)
gnomAD v4
17g.63942935G>CCA400616550SCN4Ac.4179C>G (p.Ile1393Met)
17g.63942935G>TCA501214856SCN4Ac.4179C>A (p.Ile1393=)
17g.63942935_63942936insGGCA16620555SCN4Ac.4179_4180insCC (p.Ile1394ProfsTer?)
ClinVar dbSNP
17g.63942936A>CCA400616551SCN4Ac.4178T>G (p.Ile1393Ser)
17g.63942936A>GCA400616552SCN4Ac.4178T>C (p.Ile1393Thr)
17g.63942936A>TCA400616553SCN4Ac.4178T>A (p.Ile1393Asn)
gnomAD v4
17g.63942937T>ACA400616556SCN4Ac.4177A>T (p.Ile1393Phe)
17g.63942937T>CCA400616555SCN4Ac.4177A>G (p.Ile1393Val)
dbSNP gnomAD v2 gnomAD v4
17g.63942937T>GCA400616554SCN4Ac.4177A>C (p.Ile1393Leu)
dbSNP gnomAD v4
17g.63942937T=CA2270161711SCN4Ac.4177A= (p.Ile1393=)
17g.63942938G>ACA501214857SCN4Ac.4176C>T (p.Phe1392=)
17g.63942938G>CCA400616557SCN4Ac.4176C>G (p.Phe1392Leu)
17g.63942938G>TCA400616558SCN4Ac.4176C>A (p.Phe1392Leu)
17g.63942939A=CA2270161712SCN4Ac.4175T= (p.Phe1392=)
17g.63942939A>CCA400616559SCN4Ac.4175T>G (p.Phe1392Cys)
17g.63942939A>GCA400616560SCN4Ac.4175T>C (p.Phe1392Ser)
ClinVar dbSNP
17g.63942939A>TCA400616561SCN4Ac.4175T>A (p.Phe1392Tyr)
17g.63942940A>CCA400616562SCN4Ac.4174T>G (p.Phe1392Val)
17g.63942940A>GCA400616563SCN4Ac.4174T>C (p.Phe1392Leu)
gnomAD v4
17g.63942940A>TCA400616564SCN4Ac.4174T>A (p.Phe1392Ile)
17g.63942941G>ACA501214859SCN4Ac.4173C>T (p.Ile1391=)
17g.63942941G>CCA400616565SCN4Ac.4173C>G (p.Ile1391Met)
COSMIC
17g.63942941G>TCA501214860SCN4Ac.4173C>A (p.Ile1391=)
17g.63942942A=CA2270161713SCN4Ac.4172T= (p.Ile1391=)
17g.63942942A>CCA400616566SCN4Ac.4172T>G (p.Ile1391Ser)
17g.63942942A>GCA400616567SCN4Ac.4172T>C (p.Ile1391Thr)
gnomAD v4
17g.63942942A>TCA400616568SCN4Ac.4172T>A (p.Ile1391Asn)
dbSNP gnomAD v2 gnomAD v4
17g.63942943T>ACA400616570SCN4Ac.4171A>T (p.Ile1391Phe)
dbSNP gnomAD v2 gnomAD v4
17g.63942943T>CCA292958196SCN4Ac.4171A>G (p.Ile1391Val)
ClinVar dbSNP
17g.63942943T>GCA400616569SCN4Ac.4171A>C (p.Ile1391Leu)
17g.63942943T=CA2270161714SCN4Ac.4171A= (p.Ile1391=)
17g.63942944C>ACA400616571SCN4Ac.4170G>T (p.Met1390Ile)
17g.63942944C>GCA400616572SCN4Ac.4170G>C (p.Met1390Ile)
17g.63942944C>TCA400616573SCN4Ac.4170G>A (p.Met1390Ile)
gnomAD v4
17g.63942945A>CCA400616574SCN4Ac.4169T>G (p.Met1390Arg)
ClinVar
17g.63942945A>GCA400616575SCN4Ac.4169T>C (p.Met1390Thr)
17g.63942945A>TCA400616576SCN4Ac.4169T>A (p.Met1390Lys)
17g.63942946T>ACA8709043SCN4Ac.4168A>T (p.Met1390Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63942946T>CCA400616577SCN4Ac.4168A>G (p.Met1390Val)
ClinVar dbSNP
17g.63942946T>GCA400616578SCN4Ac.4168A>C (p.Met1390Leu)
ClinVar
17g.63942946T=CA2270161715SCN4Ac.4168A= (p.Met1390=)
17g.63942947G>ACA501214861SCN4Ac.4167C>T (p.Asn1389=)
ClinVar dbSNP
17g.63942947G>CCA400616579SCN4Ac.4167C>G (p.Asn1389Lys)
17g.63942947G=CA2270161716SCN4Ac.4167C= (p.Asn1389=)
17g.63942947G>TCA400616580SCN4Ac.4167C>A (p.Asn1389Lys)
ClinVar dbSNP

Number of alleles fetched