Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.63941409C>ACA400614674SCN4Ac.4873G>T (p.Glu1625Ter)
dbSNP
17g.63941409C=CA2270160929SCN4Ac.4873G= (p.Glu1625=)
17g.63941409C>GCA400614677SCN4Ac.4873G>C (p.Glu1625Gln)
17g.63941409C>TCA400614680SCN4Ac.4873G>A (p.Glu1625Lys)
dbSNP gnomAD v3 gnomAD v4
17g.63941410C>ACA8708890SCN4Ac.4872G>T (p.Trp1624Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941410C=CA2270160930SCN4Ac.4872G= (p.Trp1624=)
17g.63941410C>GCA400614683SCN4Ac.4872G>C (p.Trp1624Cys)
17g.63941410C>TCA400614685SCN4Ac.4872G>A (p.Trp1624Ter)
dbSNP
17g.63941411C>ACA400614689SCN4Ac.4871G>T (p.Trp1624Leu)
17g.63941411C>GCA400614691SCN4Ac.4871G>C (p.Trp1624Ser)
17g.63941411C>TCA400614693SCN4Ac.4871G>A (p.Trp1624Ter)
17g.63941412A>CCA400614696SCN4Ac.4870T>G (p.Trp1624Gly)
17g.63941412A>GCA400614698SCN4Ac.4870T>C (p.Trp1624Arg)
ClinVar gnomAD v4
17g.63941412A>TCA400614700SCN4Ac.4870T>A (p.Trp1624Arg)
17g.63941413T>ACA501348512SCN4Ac.4869A>T (p.Thr1623=)
gnomAD v4
17g.63941413T>CCA146051SCN4Ac.4869A>G (p.Thr1623=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941413T>GCA501348514SCN4Ac.4869A>C (p.Thr1623=)
17g.63941413T=CA2270160931SCN4Ac.4869A= (p.Thr1623=)
17g.63941414G>ACA400614707SCN4Ac.4868C>T (p.Thr1623Ile)
dbSNP gnomAD v2 gnomAD v4
17g.63941414G>CCA400614705SCN4Ac.4868C>G (p.Thr1623Arg)
17g.63941414G=CA2270160932SCN4Ac.4868C= (p.Thr1623=)
17g.63941414G>TCA400614709SCN4Ac.4868C>A (p.Thr1623Lys)
17g.63941415T>ACA400614712SCN4Ac.4867A>T (p.Thr1623Ser)
17g.63941415T>CCA400614716SCN4Ac.4867A>G (p.Thr1623Ala)
17g.63941415T>GCA400614714SCN4Ac.4867A>C (p.Thr1623Pro)
17g.63941416C>ACA400614719SCN4Ac.4866G>T (p.Glu1622Asp)
17g.63941416C>GCA400614721SCN4Ac.4866G>C (p.Glu1622Asp)
17g.63941416C>TCA501348520SCN4Ac.4866G>A (p.Glu1622=)
17g.63941417T>ACA400614724SCN4Ac.4865A>T (p.Glu1622Val)
17g.63941417T>CCA400614727SCN4Ac.4865A>G (p.Glu1622Gly)
17g.63941417T>GCA400614729SCN4Ac.4865A>C (p.Glu1622Ala)
17g.63941418C>ACA400614732SCN4Ac.4864G>T (p.Glu1622Ter)
dbSNP
17g.63941418C=CA2270160933SCN4Ac.4864G= (p.Glu1622=)
17g.63941418C>GCA400614734SCN4Ac.4864G>C (p.Glu1622Gln)
dbSNP gnomAD v4
17g.63941418C>TCA8708891SCN4Ac.4864G>A (p.Glu1622Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941419G>ACA8708892SCN4Ac.4863C>T (p.Tyr1621=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941419G>CCA400614740SCN4Ac.4863C>G (p.Tyr1621Ter)
17g.63941419G=CA2270160934SCN4Ac.4863C= (p.Tyr1621=)
17g.63941419G>TCA400614742SCN4Ac.4863C>A (p.Tyr1621Ter)
17g.63941420T>ACA400614750SCN4Ac.4862A>T (p.Tyr1621Phe)
17g.63941420T>CCA400614748SCN4Ac.4862A>G (p.Tyr1621Cys)
17g.63941420T>GCA400614746SCN4Ac.4862A>C (p.Tyr1621Ser)
17g.63941421A>CCA400614751SCN4Ac.4861T>G (p.Tyr1621Asp)
17g.63941421A>GCA400614754SCN4Ac.4861T>C (p.Tyr1621His)
17g.63941421A>TCA400614756SCN4Ac.4861T>A (p.Tyr1621Asn)
17g.63941422G>ACA501348529SCN4Ac.4860C>T (p.Phe1620=)
17g.63941422G>CCA400614759SCN4Ac.4860C>G (p.Phe1620Leu)
17g.63941422G>TCA400614761SCN4Ac.4860C>A (p.Phe1620Leu)
17g.63941423A>CCA400614763SCN4Ac.4859T>G (p.Phe1620Cys)
17g.63941423A>GCA400614766SCN4Ac.4859T>C (p.Phe1620Ser)
17g.63941423A>TCA400614769SCN4Ac.4859T>A (p.Phe1620Tyr)
17g.63941424A>CCA400614771SCN4Ac.4858T>G (p.Phe1620Val)
17g.63941424A>GCA400614774SCN4Ac.4858T>C (p.Phe1620Leu)
gnomAD v4
17g.63941424A>TCA400614776SCN4Ac.4858T>A (p.Phe1620Ile)
17g.63941425C>ACA400614783SCN4Ac.4857G>T (p.Met1619Ile)
17g.63941425C>GCA400614781SCN4Ac.4857G>C (p.Met1619Ile)
17g.63941425C>TCA400614779SCN4Ac.4857G>A (p.Met1619Ile)
17g.63941426A=CA2270160935SCN4Ac.4856T= (p.Met1619=)
17g.63941426A>CCA400614786SCN4Ac.4856T>G (p.Met1619Arg)
17g.63941426A>GCA292956828SCN4Ac.4856T>C (p.Met1619Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63941426A>TCA400614789SCN4Ac.4856T>A (p.Met1619Lys)
dbSNP gnomAD v2 gnomAD v4
17g.63941427T>ACA292956829SCN4Ac.4855A>T (p.Met1619Leu)
dbSNP
17g.63941427T>CCA400614792SCN4Ac.4855A>G (p.Met1619Val)
dbSNP
17g.63941427T>GCA400614795SCN4Ac.4855A>C (p.Met1619Leu)
17g.63941427T=CA2270160936SCN4Ac.4855A= (p.Met1619=)
17g.63941428C>ACA400614798SCN4Ac.4854G>T (p.Glu1618Asp)
17g.63941428C>GCA400614800SCN4Ac.4854G>C (p.Glu1618Asp)
17g.63941428C>TCA501348539SCN4Ac.4854G>A (p.Glu1618=)
gnomAD v4
17g.63941429T>ACA400614804SCN4Ac.4853A>T (p.Glu1618Val)
17g.63941429T>CCA400614806SCN4Ac.4853A>G (p.Glu1618Gly)
17g.63941429T>GCA400614808SCN4Ac.4853A>C (p.Glu1618Ala)
17g.63941430C>ACA400614815SCN4Ac.4852G>T (p.Glu1618Ter)
dbSNP
17g.63941430C=CA2270160937SCN4Ac.4852G= (p.Glu1618=)
17g.63941430C>GCA400614812SCN4Ac.4852G>C (p.Glu1618Gln)
17g.63941430C>TCA400614811SCN4Ac.4852G>A (p.Glu1618Lys)
17g.63941431A=CA2270160938SCN4Ac.4851T= (p.Phe1617=)
17g.63941431A>CCA400614818SCN4Ac.4851T>G (p.Phe1617Leu)
gnomAD v4
17g.63941431A>GCA501348543SCN4Ac.4851T>C (p.Phe1617=)
17g.63941431A>TCA8708893SCN4Ac.4851T>A (p.Phe1617Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.63941432A>CCA400614823SCN4Ac.4850T>G (p.Phe1617Cys)
17g.63941432A>GCA400614825SCN4Ac.4850T>C (p.Phe1617Ser)
17g.63941432A>TCA400614828SCN4Ac.4850T>A (p.Phe1617Tyr)
17g.63941433A>CCA400614832SCN4Ac.4849T>G (p.Phe1617Val)
17g.63941433A>GCA400614834SCN4Ac.4849T>C (p.Phe1617Leu)
17g.63941433A>TCA400614835SCN4Ac.4849T>A (p.Phe1617Ile)
17g.63941434G>ACA501348545SCN4Ac.4848C>T (p.Asp1616=)
17g.63941434G>CCA400614836SCN4Ac.4848C>G (p.Asp1616Glu)
17g.63941434G>TCA400614837SCN4Ac.4848C>A (p.Asp1616Glu)
17g.63941435T>ACA400614838SCN4Ac.4847A>T (p.Asp1616Val)
17g.63941435T>CCA400614839SCN4Ac.4847A>G (p.Asp1616Gly)
17g.63941435T>GCA400614840SCN4Ac.4847A>C (p.Asp1616Ala)
17g.63941436C>ACA400614842SCN4Ac.4846G>T (p.Asp1616Tyr)
17g.63941436C>GCA400614843SCN4Ac.4846G>C (p.Asp1616His)
17g.63941436C>TCA400614841SCN4Ac.4846G>A (p.Asp1616Asn)
17g.63941437A=CA2270160939SCN4Ac.4845T= (p.Asp1615=)
17g.63941437A>CCA400614845SCN4Ac.4845T>G (p.Asp1615Glu)
17g.63941437A>GCA501348552SCN4Ac.4845T>C (p.Asp1615=)
dbSNP gnomAD v3 gnomAD v4
17g.63941437A>TCA400614844SCN4Ac.4845T>A (p.Asp1615Glu)
17g.63941438T>ACA400614846SCN4Ac.4844A>T (p.Asp1615Val)
17g.63941438T>CCA400614847SCN4Ac.4844A>G (p.Asp1615Gly)
ClinVar dbSNP
17g.63941438T>GCA400614848SCN4Ac.4844A>C (p.Asp1615Ala)
17g.63941439C>ACA400614849SCN4Ac.4843G>T (p.Asp1615Tyr)
gnomAD v4
17g.63941439C>GCA400614850SCN4Ac.4843G>C (p.Asp1615His)
17g.63941439C>TCA400614851SCN4Ac.4843G>A (p.Asp1615Asn)
17g.63941440T>ACA400614852SCN4Ac.4842A>T (p.Glu1614Asp)
dbSNP gnomAD v2 gnomAD v4
17g.63941440T>CCA501348558SCN4Ac.4842A>G (p.Glu1614=)
17g.63941440T>GCA400614853SCN4Ac.4842A>C (p.Glu1614Asp)
17g.63941440T=CA2270160940SCN4Ac.4842A= (p.Glu1614=)
17g.63941441T>ACA400614854SCN4Ac.4841A>T (p.Glu1614Val)
17g.63941441T>CCA400614855SCN4Ac.4841A>G (p.Glu1614Gly)
17g.63941441T>GCA400614856SCN4Ac.4841A>C (p.Glu1614Ala)
17g.63941442C>ACA400614859SCN4Ac.4840G>T (p.Glu1614Ter)
dbSNP
17g.63941442C=CA2270160941SCN4Ac.4840G= (p.Glu1614=)
17g.63941442C>GCA400614857SCN4Ac.4840G>C (p.Glu1614Gln)
17g.63941442C>TCA400614858SCN4Ac.4840G>A (p.Glu1614Lys)
COSMIC
17g.63941443A>CCA501348567SCN4Ac.4839T>G (p.Gly1613=)
17g.63941443A>GCA501348565SCN4Ac.4839T>C (p.Gly1613=)
17g.63941443A>TCA501348569SCN4Ac.4839T>A (p.Gly1613=)
17g.63941444C>ACA400614860SCN4Ac.4838G>T (p.Gly1613Val)
dbSNP
17g.63941444C=CA2270160942SCN4Ac.4838G= (p.Gly1613=)
17g.63941444C>GCA400614861SCN4Ac.4838G>C (p.Gly1613Ala)
17g.63941444C>TCA400614862SCN4Ac.4838G>A (p.Gly1613Asp)
17g.63941445C>ACA400614863SCN4Ac.4837G>T (p.Gly1613Cys)
gnomAD v3 gnomAD v4
17g.63941445C=CA2270160943SCN4Ac.4837G= (p.Gly1613=)
17g.63941445C>GCA8708894SCN4Ac.4837G>C (p.Gly1613Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941445C>TCA400614864SCN4Ac.4837G>A (p.Gly1613Ser)
17g.63941446A=CA2270160944SCN4Ac.4836T= (p.Leu1612=)
17g.63941446A>CCA501348574SCN4Ac.4836T>G (p.Leu1612=)
17g.63941446A>GCA501348575SCN4Ac.4836T>C (p.Leu1612=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.63941446A>TCA501348576SCN4Ac.4836T>A (p.Leu1612=)
ClinVar dbSNP
17g.63941447A=CA2270160945SCN4Ac.4835T= (p.Leu1612=)
17g.63941447A>CCA400614865SCN4Ac.4835T>G (p.Leu1612Arg)
gnomAD v4
17g.63941447A>GCA400614866SCN4Ac.4835T>C (p.Leu1612Pro)
gnomAD v4
17g.63941447A>TCA400614867SCN4Ac.4835T>A (p.Leu1612His)
dbSNP gnomAD v4
17g.63941448G>ACA400614868SCN4Ac.4834C>T (p.Leu1612Phe)
17g.63941448G>CCA400614869SCN4Ac.4834C>G (p.Leu1612Val)
17g.63941448G>TCA400614870SCN4Ac.4834C>A (p.Leu1612Ile)
17g.63941449G>ACA501348586SCN4Ac.4833C>T (p.Pro1611=)
17g.63941449G>CCA501348587SCN4Ac.4833C>G (p.Pro1611=)
ClinVar
17g.63941449G>TCA501348588SCN4Ac.4833C>A (p.Pro1611=)
17g.63941450G>ACA400614872SCN4Ac.4832C>T (p.Pro1611Leu)
17g.63941450G>CCA400614873SCN4Ac.4832C>G (p.Pro1611Arg)
17g.63941450G>TCA400614871SCN4Ac.4832C>A (p.Pro1611His)
17g.63941451G>ACA400614874SCN4Ac.4831C>T (p.Pro1611Ser)
17g.63941451G>CCA400614875SCN4Ac.4831C>G (p.Pro1611Ala)
17g.63941451G=CA2270160946SCN4Ac.4831C= (p.Pro1611=)
17g.63941451G>TCA8708895SCN4Ac.4831C>A (p.Pro1611Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.63941452C>ACA400614876SCN4Ac.4830G>T (p.Glu1610Asp)
17g.63941452C>GCA400614877SCN4Ac.4830G>C (p.Glu1610Asp)
17g.63941452C>TCA501348600SCN4Ac.4830G>A (p.Glu1610=)
17g.63941453T>ACA400614880SCN4Ac.4829A>T (p.Glu1610Val)
17g.63941453T>CCA400614879SCN4Ac.4829A>G (p.Glu1610Gly)
COSMIC
17g.63941453T>GCA400614878SCN4Ac.4829A>C (p.Glu1610Ala)
17g.63941454C>ACA400614881SCN4Ac.4828G>T (p.Glu1610Ter)
dbSNP
17g.63941454C=CA2270160947SCN4Ac.4828G= (p.Glu1610=)
17g.63941454C>GCA400614882SCN4Ac.4828G>C (p.Glu1610Gln)
17g.63941454C>TCA8708896SCN4Ac.4828G>A (p.Glu1610Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941455G>ACA292956831SCN4Ac.4827C>T (p.Ser1609=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.63941455G>CCA400614883SCN4Ac.4827C>G (p.Ser1609Arg)
ClinVar
17g.63941455G=CA2270160948SCN4Ac.4827C= (p.Ser1609=)
17g.63941455G>TCA400614884SCN4Ac.4827C>A (p.Ser1609Arg)
gnomAD v4
17g.63941456C>ACA400614885SCN4Ac.4826G>T (p.Ser1609Ile)
17g.63941456C>GCA400614887SCN4Ac.4826G>C (p.Ser1609Thr)
17g.63941456C>TCA400614886SCN4Ac.4826G>A (p.Ser1609Asn)
gnomAD v4
17g.63941457T>ACA400614888SCN4Ac.4825A>T (p.Ser1609Cys)
17g.63941457T>CCA400614889SCN4Ac.4825A>G (p.Ser1609Gly)
17g.63941457T>GCA400614890SCN4Ac.4825A>C (p.Ser1609Arg)
ClinVar dbSNP gnomAD v4
17g.63941457T=CA2270160949SCN4Ac.4825A= (p.Ser1609=)
17g.63941458G>ACA501348611SCN4Ac.4824C>T (p.Ser1608=)
gnomAD v4
17g.63941458G>CCA400614891SCN4Ac.4824C>G (p.Ser1608Arg)
17g.63941458G>TCA400614892SCN4Ac.4824C>A (p.Ser1608Arg)
17g.63941459C>ACA400614893SCN4Ac.4823G>T (p.Ser1608Ile)
17g.63941459C=CA2270160950SCN4Ac.4823G= (p.Ser1608=)
17g.63941459C>GCA400614894SCN4Ac.4823G>C (p.Ser1608Thr)
ClinVar dbSNP
17g.63941459C>TCA400614895SCN4Ac.4823G>A (p.Ser1608Asn)
17g.63941460T>ACA400614896SCN4Ac.4822A>T (p.Ser1608Cys)
17g.63941460T>CCA400614897SCN4Ac.4822A>G (p.Ser1608Gly)
17g.63941460T>GCA400614898SCN4Ac.4822A>C (p.Ser1608Arg)
17g.63941461C>ACA400614899SCN4Ac.4821G>T (p.Glu1607Asp)
17g.63941461C=CA2270160951SCN4Ac.4821G= (p.Glu1607=)
17g.63941461C>GCA400614900SCN4Ac.4821G>C (p.Glu1607Asp)
dbSNP gnomAD v4
17g.63941461C>TCA501348613SCN4Ac.4821G>A (p.Glu1607=)
17g.63941464_63941466delCA2695226827SCN4Ac.4819_4821del (p.Glu1607del)
17g.63941462T>ACA400614902SCN4Ac.4820A>T (p.Glu1607Val)
17g.63941462T>CCA400614903SCN4Ac.4820A>G (p.Glu1607Gly)
17g.63941462T>GCA400614901SCN4Ac.4820A>C (p.Glu1607Ala)
17g.63941463C>ACA400614905SCN4Ac.4819G>T (p.Glu1607Ter)
dbSNP
17g.63941463C=CA2270160952SCN4Ac.4819G= (p.Glu1607=)
17g.63941463C>GCA400614904SCN4Ac.4819G>C (p.Glu1607Gln)
17g.63941463C>TCA8708897SCN4Ac.4819G>A (p.Glu1607Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941464C>ACA400614906SCN4Ac.4818G>T (p.Glu1606Asp)
17g.63941464C>GCA400614907SCN4Ac.4818G>C (p.Glu1606Asp)
17g.63941464C>TCA501348614SCN4Ac.4818G>A (p.Glu1606=)
17g.63941465T>ACA400614908SCN4Ac.4817A>T (p.Glu1606Val)
17g.63941465T>CCA400614909SCN4Ac.4817A>G (p.Glu1606Gly)
17g.63941465T>GCA400614910SCN4Ac.4817A>C (p.Glu1606Ala)
17g.63941466C>ACA400614911SCN4Ac.4816G>T (p.Glu1606Ter)
dbSNP
17g.63941466C=CA2270160953SCN4Ac.4816G= (p.Glu1606=)
17g.63941466C>GCA400614912SCN4Ac.4816G>C (p.Glu1606Gln)
17g.63941466C>TCA400614913SCN4Ac.4816G>A (p.Glu1606Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63941467T>ACA8708898SCN4Ac.4815A>T (p.Thr1605=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.63941467T>CCA501348615SCN4Ac.4815A>G (p.Thr1605=)
17g.63941467T>GCA501348616SCN4Ac.4815A>C (p.Thr1605=)
17g.63941467T=CA2270160954SCN4Ac.4815A= (p.Thr1605=)
17g.63941468G>ACA400614914SCN4Ac.4814C>T (p.Thr1605Ile)
ClinVar dbSNP gnomAD v4
17g.63941468G>CCA400614915SCN4Ac.4814C>G (p.Thr1605Arg)
17g.63941468G=CA2270160955SCN4Ac.4814C= (p.Thr1605=)
17g.63941468G>TCA400614916SCN4Ac.4814C>A (p.Thr1605Lys)
17g.63941469T>ACA400614919SCN4Ac.4813A>T (p.Thr1605Ser)
17g.63941469T>CCA400614918SCN4Ac.4813A>G (p.Thr1605Ala)
17g.63941469T>GCA400614917SCN4Ac.4813A>C (p.Thr1605Pro)
17g.63941470G>ACA501347951SCN4Ac.4812C>T (p.Ala1604=)
17g.63941470G>CCA501347953SCN4Ac.4812C>G (p.Ala1604=)
17g.63941470G>TCA501347952SCN4Ac.4812C>A (p.Ala1604=)
17g.63941471G>ACA400614920SCN4Ac.4811C>T (p.Ala1604Val)
17g.63941471G>CCA400614921SCN4Ac.4811C>G (p.Ala1604Gly)
17g.63941471G>TCA400614922SCN4Ac.4811C>A (p.Ala1604Asp)
17g.63941472C>ACA400614923SCN4Ac.4810G>T (p.Ala1604Ser)
17g.63941472C>GCA400614924SCN4Ac.4810G>C (p.Ala1604Pro)
17g.63941472C>TCA400614925SCN4Ac.4810G>A (p.Ala1604Thr)
17g.63941473C>ACA501347964SCN4Ac.4809G>T (p.Val1603=)
17g.63941473C=CA2270160956SCN4Ac.4809G= (p.Val1603=)
17g.63941473C>GCA501347965SCN4Ac.4809G>C (p.Val1603=)
17g.63941473C>TCA8708899SCN4Ac.4809G>A (p.Val1603=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.63941474A>CCA400614926SCN4Ac.4808T>G (p.Val1603Gly)
17g.63941474A>GCA400614927SCN4Ac.4808T>C (p.Val1603Ala)
17g.63941474A>TCA400614928SCN4Ac.4808T>A (p.Val1603Glu)
17g.63941475C>ACA400614929SCN4Ac.4807G>T (p.Val1603Leu)
17g.63941475C>GCA400614930SCN4Ac.4807G>C (p.Val1603Leu)
17g.63941475C>TCA400614931SCN4Ac.4807G>A (p.Val1603Met)
gnomAD v4
17g.63941476A=CA2270160957SCN4Ac.4806T= (p.Asn1602=)
17g.63941476A>CCA400614932SCN4Ac.4806T>G (p.Asn1602Lys)
17g.63941476A>GCA501347984SCN4Ac.4806T>C (p.Asn1602=)
dbSNP gnomAD v4
17g.63941476A>TCA400614933SCN4Ac.4806T>A (p.Asn1602Lys)
17g.63941477T>ACA400614934SCN4Ac.4805A>T (p.Asn1602Ile)
17g.63941477T>CCA8708900SCN4Ac.4805A>G (p.Asn1602Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941477T>GCA400614935SCN4Ac.4805A>C (p.Asn1602Thr)
17g.63941477T=CA2270160958SCN4Ac.4805A= (p.Asn1602=)
17g.63941478T>ACA400614936SCN4Ac.4804A>T (p.Asn1602Tyr)
17g.63941478T>CCA400614937SCN4Ac.4804A>G (p.Asn1602Asp)
17g.63941478T>GCA400614938SCN4Ac.4804A>C (p.Asn1602His)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63941478T=CA2270160959SCN4Ac.4804A= (p.Asn1602=)
17g.63941479G>ACA501347987SCN4Ac.4803C>T (p.Phe1601=)
17g.63941479G>CCA400614939SCN4Ac.4803C>G (p.Phe1601Leu)
17g.63941479G>TCA400614940SCN4Ac.4803C>A (p.Phe1601Leu)
17g.63941480A>CCA400614941SCN4Ac.4802T>G (p.Phe1601Cys)
17g.63941480A>GCA400614942SCN4Ac.4802T>C (p.Phe1601Ser)
17g.63941480A>TCA400614943SCN4Ac.4802T>A (p.Phe1601Tyr)
17g.63941481A>CCA400614944SCN4Ac.4801T>G (p.Phe1601Val)
17g.63941481A>GCA400614945SCN4Ac.4801T>C (p.Phe1601Leu)
17g.63941481A>TCA400614946SCN4Ac.4801T>A (p.Phe1601Ile)
17g.63941482G>ACA501348001SCN4Ac.4800C>T (p.Asn1600=)
17g.63941482G>CCA400614948SCN4Ac.4800C>G (p.Asn1600Lys)
17g.63941482G>TCA400614947SCN4Ac.4800C>A (p.Asn1600Lys)
COSMIC
17g.63941483T>ACA400614949SCN4Ac.4799A>T (p.Asn1600Ile)
17g.63941483T>CCA400614950SCN4Ac.4799A>G (p.Asn1600Ser)
dbSNP gnomAD v2 gnomAD v4
17g.63941483T>GCA400614951SCN4Ac.4799A>C (p.Asn1600Thr)
17g.63941483T=CA2270160960SCN4Ac.4799A= (p.Asn1600=)
17g.63941484T>ACA400614952SCN4Ac.4798A>T (p.Asn1600Tyr)
17g.63941484T>CCA400614953SCN4Ac.4798A>G (p.Asn1600Asp)
gnomAD v4 COSMIC
17g.63941484T>GCA400614954SCN4Ac.4798A>C (p.Asn1600His)
17g.63941485C>ACA400614956SCN4Ac.4797G>T (p.Glu1599Asp)
17g.63941485C>GCA400614955SCN4Ac.4797G>C (p.Glu1599Asp)
17g.63941485C>TCA501348009SCN4Ac.4797G>A (p.Glu1599=)
17g.63941486T>ACA400614957SCN4Ac.4796A>T (p.Glu1599Val)
17g.63941486T>CCA400614958SCN4Ac.4796A>G (p.Glu1599Gly)
17g.63941486T>GCA400614959SCN4Ac.4796A>C (p.Glu1599Ala)
17g.63941487C>ACA400614960SCN4Ac.4795G>T (p.Glu1599Ter)
dbSNP
17g.63941487C=CA2270160961SCN4Ac.4795G= (p.Glu1599=)
17g.63941487C>GCA400614961SCN4Ac.4795G>C (p.Glu1599Gln)
17g.63941487C>TCA400614962SCN4Ac.4795G>A (p.Glu1599Lys)
17g.63941488C>ACA501348017SCN4Ac.4794G>T (p.Leu1598=)
17g.63941488C=CA2270160962SCN4Ac.4794G= (p.Leu1598=)
17g.63941488C>GCA501348018SCN4Ac.4794G>C (p.Leu1598=)
17g.63941488C>TCA501348019SCN4Ac.4794G>A (p.Leu1598=)
dbSNP gnomAD v3 gnomAD v4
17g.63941489A>CCA400614963SCN4Ac.4793T>G (p.Leu1598Arg)
17g.63941489A>GCA400614965SCN4Ac.4793T>C (p.Leu1598Pro)
17g.63941489A>TCA400614964SCN4Ac.4793T>A (p.Leu1598Gln)
17g.63941490G>ACA501348021SCN4Ac.4792C>T (p.Leu1598=)
17g.63941490G>CCA400614966SCN4Ac.4792C>G (p.Leu1598Val)
17g.63941490G>TCA400614967SCN4Ac.4792C>A (p.Leu1598Met)
gnomAD v4
17g.63941491G>ACA501348023SCN4Ac.4791C>T (p.Ile1597=)
17g.63941491G>CCA400614968SCN4Ac.4791C>G (p.Ile1597Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.63941491G=CA2270160963SCN4Ac.4791C= (p.Ile1597=)
17g.63941491G>TCA501348025SCN4Ac.4791C>A (p.Ile1597=)
17g.63941492A>CCA400614969SCN4Ac.4790T>G (p.Ile1597Ser)
17g.63941492A>GCA400614970SCN4Ac.4790T>C (p.Ile1597Thr)
17g.63941492A>TCA400614971SCN4Ac.4790T>A (p.Ile1597Asn)
gnomAD v4
17g.63941493T>ACA400614972SCN4Ac.4789A>T (p.Ile1597Phe)
17g.63941493T>CCA400614973SCN4Ac.4789A>G (p.Ile1597Val)
17g.63941493T>GCA400614974SCN4Ac.4789A>C (p.Ile1597Leu)
17g.63941494G>ACA501348032SCN4Ac.4788C>T (p.Ile1596=)
COSMIC
17g.63941494G>CCA400614975SCN4Ac.4788C>G (p.Ile1596Met)
17g.63941494G>TCA501348034SCN4Ac.4788C>A (p.Ile1596=)
17g.63941495A>CCA400614976SCN4Ac.4787T>G (p.Ile1596Ser)
17g.63941495A>GCA400614977SCN4Ac.4787T>C (p.Ile1596Thr)
17g.63941495A>TCA400614978SCN4Ac.4787T>A (p.Ile1596Asn)
17g.63941496T>ACA400614979SCN4Ac.4786A>T (p.Ile1596Phe)
17g.63941496T>CCA400614980SCN4Ac.4786A>G (p.Ile1596Val)
17g.63941496T>GCA400614981SCN4Ac.4786A>C (p.Ile1596Leu)
dbSNP
17g.63941496T=CA2270160964SCN4Ac.4786A= (p.Ile1596=)
17g.63941497G>ACA501348036SCN4Ac.4785C>T (p.Ala1595=)
17g.63941497G>CCA501348037SCN4Ac.4785C>G (p.Ala1595=)
17g.63941497G>TCA501348038SCN4Ac.4785C>A (p.Ala1595=)
17g.63941498G>ACA400614982SCN4Ac.4784C>T (p.Ala1595Val)
ClinVar dbSNP gnomAD v4
17g.63941498G>CCA400614984SCN4Ac.4784C>G (p.Ala1595Gly)
17g.63941498G=CA2270160965SCN4Ac.4784C= (p.Ala1595=)
17g.63941498G>TCA400614983SCN4Ac.4784C>A (p.Ala1595Asp)
17g.63941499C>ACA400614985SCN4Ac.4783G>T (p.Ala1595Ser)
ClinVar dbSNP
17g.63941499C=CA2270160966SCN4Ac.4783G= (p.Ala1595=)
17g.63941499C>GCA400614986SCN4Ac.4783G>C (p.Ala1595Pro)
17g.63941499C>TCA8708901SCN4Ac.4783G>A (p.Ala1595Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.63941500G>ACA8708902SCN4Ac.4782C>T (p.Ile1594=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941500G>CCA400614987SCN4Ac.4782C>G (p.Ile1594Met)
17g.63941500G=CA2270160967SCN4Ac.4782C= (p.Ile1594=)
17g.63941500G>TCA501348046SCN4Ac.4782C>A (p.Ile1594=)
17g.63941501A>CCA400614988SCN4Ac.4781T>G (p.Ile1594Ser)
17g.63941501A>GCA400614989SCN4Ac.4781T>C (p.Ile1594Thr)
17g.63941501A>TCA400614990SCN4Ac.4781T>A (p.Ile1594Asn)
ClinVar
17g.63941502T>ACA400614991SCN4Ac.4780A>T (p.Ile1594Phe)
17g.63941502T>CCA8708903SCN4Ac.4780A>G (p.Ile1594Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.63941502T>GCA400614992SCN4Ac.4780A>C (p.Ile1594Leu)
17g.63941502T=CA2270160968SCN4Ac.4780A= (p.Ile1594=)
17g.63941503G>ACA501348051SCN4Ac.4779C>T (p.Tyr1593=)
17g.63941503G>CCA400614994SCN4Ac.4779C>G (p.Tyr1593Ter)
17g.63941503G>TCA400614993SCN4Ac.4779C>A (p.Tyr1593Ter)
ClinVar
17g.63941504T>ACA400614995SCN4Ac.4778A>T (p.Tyr1593Phe)
ClinVar dbSNP
17g.63941504T>CCA400614997SCN4Ac.4778A>G (p.Tyr1593Cys)
17g.63941504T>GCA400614996SCN4Ac.4778A>C (p.Tyr1593Ser)
17g.63941504T=CA2270160969SCN4Ac.4778A= (p.Tyr1593=)
17g.63941505A>CCA400614998SCN4Ac.4777T>G (p.Tyr1593Asp)
17g.63941505A>GCA400614999SCN4Ac.4777T>C (p.Tyr1593His)
17g.63941505A>TCA400615000SCN4Ac.4777T>A (p.Tyr1593Asn)
17g.63941506C>ACA10603317SCN4Ac.4776G>T (p.Met1592Ile)
ClinVar dbSNP
17g.63941506C=CA2270160970SCN4Ac.4776G= (p.Met1592=)
17g.63941506C>GCA400615001SCN4Ac.4776G>C (p.Met1592Ile)
17g.63941506C>TCA400615002SCN4Ac.4776G>A (p.Met1592Ile)
ClinVar dbSNP
17g.63941507A>CCA400615003SCN4Ac.4775T>G (p.Met1592Arg)
17g.63941507A>GCA400615004SCN4Ac.4775T>C (p.Met1592Thr)
gnomAD v4
17g.63941507A>TCA400615005SCN4Ac.4775T>A (p.Met1592Lys)
17g.63941508T>ACA400615006SCN4Ac.4774A>T (p.Met1592Leu)
17g.63941508T>CCA117834SCN4Ac.4774A>G (p.Met1592Val)
ClinVar dbSNP
17g.63941508T>GCA400615007SCN4Ac.4774A>C (p.Met1592Leu)
17g.63941508T=CA2270160971SCN4Ac.4774A= (p.Met1592=)
17g.63941509G>ACA501348061SCN4Ac.4773C>T (p.Asn1591=)
dbSNP gnomAD v2 gnomAD v4
17g.63941509G>CCA400615008SCN4Ac.4773C>G (p.Asn1591Lys)
17g.63941509G=CA2270160972SCN4Ac.4773C= (p.Asn1591=)
17g.63941509G>TCA400615009SCN4Ac.4773C>A (p.Asn1591Lys)

Number of alleles fetched