Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.20139834G>ACA10108575ZDHHC8c.499G>A (p.Gly167Ser)
c.384+199G>A (n.384+199G>A)
c.466G>A (p.Gly156Ser)
n.58-783G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
22g.20139834G>CCA410734353ZDHHC8c.499G>C (p.Gly167Arg)
c.384+199G>C (n.384+199G>C)
c.466G>C (p.Gly156Arg)
n.58-783G>C
22g.20139834G=CA2396214269ZDHHC8c.499G= (p.Gly167=)
c.384+199G= (n.384+199G=)
c.466G= (p.Gly156=)
n.58-783G=
22g.20139834G>TCA410734355ZDHHC8c.499G>T (p.Gly167Cys)
c.384+199G>T (n.384+199G>T)
c.466G>T (p.Gly156Cys)
n.58-783G>T
22g.20139835G>ACA410734358ZDHHC8c.500G>A (p.Gly167Asp)
c.384+200G>A (n.384+200G>A)
c.467G>A (p.Gly156Asp)
n.58-782G>A
22g.20139835G>CCA410734359ZDHHC8c.500G>C (p.Gly167Ala)
c.384+200G>C (n.384+200G>C)
c.467G>C (p.Gly156Ala)
n.58-782G>C
22g.20139835G>TCA410734361ZDHHC8c.500G>T (p.Gly167Val)
c.384+200G>T (n.384+200G>T)
c.467G>T (p.Gly156Val)
n.58-782G>T
22g.20139836C>ACA513691209ZDHHC8c.501C>A (p.Gly167=)
c.384+201C>A (n.384+201C>A)
c.468C>A (p.Gly156=)
n.58-781C>A
22g.20139836C=CA2396214270ZDHHC8c.501C= (p.Gly167=)
c.384+201C= (n.384+201C=)
c.468C= (p.Gly156=)
n.58-781C=
22g.20139836C>GCA513691210ZDHHC8c.501C>G (p.Gly167=)
c.384+201C>G (n.384+201C>G)
c.468C>G (p.Gly156=)
n.58-781C>G
gnomAD v4
22g.20139836C>TCA10108576ZDHHC8c.501C>T (p.Gly167=)
c.384+201C>T (n.384+201C>T)
c.468C>T (p.Gly156=)
n.58-781C>T
dbSNP ExAC gnomAD v2 gnomAD v4
22g.20139836_20139838delCA2655369130ZDHHC8c.501_503del (p.Leu168del)
c.384+201_384+203del (n.384+201_384+203del)
c.468_470del (p.Leu157del)
n.58-781_58-779del
gnomAD v4
22g.20139837C>ACA410734365ZDHHC8c.502C>A (p.Leu168Met)
c.384+202C>A (n.384+202C>A)
c.469C>A (p.Leu157Met)
n.58-780C>A
22g.20139837C>GCA410734364ZDHHC8c.502C>G (p.Leu168Val)
c.384+202C>G (n.384+202C>G)
c.469C>G (p.Leu157Val)
n.58-780C>G
22g.20139837C>TCA513691212ZDHHC8c.502C>T (p.Leu168=)
c.384+202C>T (n.384+202C>T)
c.469C>T (p.Leu157=)
n.58-780C>T
gnomAD v4
22g.20139838T>ACA410734366ZDHHC8c.503T>A (p.Leu168Gln)
c.384+203T>A (n.384+203T>A)
c.470T>A (p.Leu157Gln)
n.58-779T>A
22g.20139838T>CCA410734367ZDHHC8c.503T>C (p.Leu168Pro)
c.384+203T>C (n.384+203T>C)
c.470T>C (p.Leu157Pro)
n.58-779T>C
22g.20139838T>GCA410734369ZDHHC8c.503T>G (p.Leu168Arg)
c.384+203T>G (n.384+203T>G)
c.470T>G (p.Leu157Arg)
n.58-779T>G
gnomAD v4
22g.20139839G>ACA513691217ZDHHC8c.504G>A (p.Leu168=)
c.384+204G>A (n.384+204G>A)
c.471G>A (p.Leu157=)
n.58-778G>A
22g.20139839G>CCA513691218ZDHHC8c.504G>C (p.Leu168=)
c.384+204G>C (n.384+204G>C)
c.471G>C (p.Leu157=)
n.58-778G>C
22g.20139839G=CA2396214271ZDHHC8c.504G= (p.Leu168=)
c.384+204G= (n.384+204G=)
c.471G= (p.Leu157=)
n.58-778G=
22g.20139839G>TCA513691219ZDHHC8c.504G>T (p.Leu168=)
c.384+204G>T (n.384+204G>T)
c.471G>T (p.Leu157=)
n.58-778G>T
dbSNP gnomAD v4
22g.20139840G>ACA410734371ZDHHC8c.505G>A (p.Val169Ile)
c.384+205G>A (n.384+205G>A)
c.472G>A (p.Val158Ile)
n.58-777G>A
22g.20139840G>CCA410734373ZDHHC8c.505G>C (p.Val169Leu)
c.384+205G>C (n.384+205G>C)
c.472G>C (p.Val158Leu)
n.58-777G>C
22g.20139840G>TCA410734374ZDHHC8c.505G>T (p.Val169Phe)
c.384+205G>T (n.384+205G>T)
c.472G>T (p.Val158Phe)
n.58-777G>T
gnomAD v4
22g.20139841T>ACA410734375ZDHHC8c.506T>A (p.Val169Asp)
c.384+206T>A (n.384+206T>A)
c.473T>A (p.Val158Asp)
n.58-776T>A
22g.20139841T>CCA410734377ZDHHC8c.506T>C (p.Val169Ala)
c.384+206T>C (n.384+206T>C)
c.473T>C (p.Val158Ala)
n.58-776T>C
22g.20139841T>GCA410734379ZDHHC8c.506T>G (p.Val169Gly)
c.384+206T>G (n.384+206T>G)
c.473T>G (p.Val158Gly)
n.58-776T>G
dbSNP
22g.20139841T=CA2396214272ZDHHC8c.506T= (p.Val169=)
c.384+206T= (n.384+206T=)
c.473T= (p.Val158=)
n.58-776T=
22g.20139842C>ACA513691225ZDHHC8c.507C>A (p.Val169=)
c.384+207C>A (n.384+207C>A)
c.474C>A (p.Val158=)
n.58-775C>A
22g.20139842C>GCA513691226ZDHHC8c.507C>G (p.Val169=)
c.384+207C>G (n.384+207C>G)
c.474C>G (p.Val158=)
n.58-775C>G
22g.20139842C>TCA513691227ZDHHC8c.507C>T (p.Val169=)
c.384+207C>T (n.384+207C>T)
c.474C>T (p.Val158=)
n.58-775C>T
22g.20139843T>ACA410734381ZDHHC8c.508T>A (p.Tyr170Asn)
c.384+208T>A (n.384+208T>A)
c.475T>A (p.Tyr159Asn)
n.58-774T>A
22g.20139843T>CCA410734382ZDHHC8c.508T>C (p.Tyr170His)
c.384+208T>C (n.384+208T>C)
c.475T>C (p.Tyr159His)
n.58-774T>C
22g.20139843T>GCA410734384ZDHHC8c.508T>G (p.Tyr170Asp)
c.384+208T>G (n.384+208T>G)
c.475T>G (p.Tyr159Asp)
n.58-774T>G
22g.20139844A>CCA410734390ZDHHC8c.509A>C (p.Tyr170Ser)
c.384+209A>C (n.384+209A>C)
c.476A>C (p.Tyr159Ser)
n.58-773A>C
22g.20139844A>GCA410734388ZDHHC8c.509A>G (p.Tyr170Cys)
c.384+209A>G (n.384+209A>G)
c.476A>G (p.Tyr159Cys)
n.58-773A>G
22g.20139844A>TCA410734387ZDHHC8c.509A>T (p.Tyr170Phe)
c.384+209A>T (n.384+209A>T)
c.476A>T (p.Tyr159Phe)
n.58-773A>T
22g.20139845C>ACA410734392ZDHHC8c.510C>A (p.Tyr170Ter)
c.384+210C>A (n.384+210C>A)
c.477C>A (p.Tyr159Ter)
n.58-772C>A
gnomAD v4
22g.20139845C=CA2396214273ZDHHC8c.510C= (p.Tyr170=)
c.384+210C= (n.384+210C=)
c.477C= (p.Tyr159=)
n.58-772C=
22g.20139845C>GCA410734395ZDHHC8c.510C>G (p.Tyr170Ter)
c.384+210C>G (n.384+210C>G)
c.477C>G (p.Tyr159Ter)
n.58-772C>G
22g.20139845C>TCA10108577ZDHHC8c.510C>T (p.Tyr170=)
c.384+210C>T (n.384+210C>T)
c.477C>T (p.Tyr159=)
n.58-772C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.20139846G>ACA10108578ZDHHC8c.511G>A (p.Val171Met)
c.384+211G>A (n.384+211G>A)
c.478G>A (p.Val160Met)
n.58-771G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.20139846G>CCA410734397ZDHHC8c.511G>C (p.Val171Leu)
c.384+211G>C (n.384+211G>C)
c.478G>C (p.Val160Leu)
n.58-771G>C
22g.20139846G=CA2396214274ZDHHC8c.511G= (p.Val171=)
c.384+211G= (n.384+211G=)
c.478G= (p.Val160=)
n.58-771G=
22g.20139846G>TCA10108579ZDHHC8c.511G>T (p.Val171Leu)
c.384+211G>T (n.384+211G>T)
c.478G>T (p.Val160Leu)
n.58-771G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.20139847T>ACA410734400ZDHHC8c.512T>A (p.Val171Glu)
c.384+212T>A (n.384+212T>A)
c.479T>A (p.Val160Glu)
n.58-770T>A
22g.20139847T>CCA410734402ZDHHC8c.512T>C (p.Val171Ala)
c.384+212T>C (n.384+212T>C)
c.479T>C (p.Val160Ala)
n.58-770T>C
22g.20139847T>GCA410734403ZDHHC8c.512T>G (p.Val171Gly)
c.384+212T>G (n.384+212T>G)
c.479T>G (p.Val160Gly)
n.58-770T>G
22g.20139848G>ACA513691241ZDHHC8c.513G>A (p.Val171=)
c.384+213G>A (n.384+213G>A)
c.480G>A (p.Val160=)
n.58-769G>A

Number of alleles fetched