Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.44148538_44152555dupCA1139771162GCKc.*207-130_*678-705dup
c.209-130_680-705dup
n.695-130_2387dup
c.212-130_683-705dup
c.206-130_677-705dup
c.209-130_629-705dup
7g.44152358_44152367delCA2695203006GCKc.*272_*281del (n.*272_*281del)
c.274_283del (p.Gly92ArgfsTer7)
n.760_769del
c.277_286del (p.Gly93ArgfsTer7)
c.271_280del (p.Gly91ArgfsTer7)
7g.44152361_44152370delCA2695203007GCKc.*264_*273del (n.*264_*273del)
c.266_275del (p.Val89GlufsTer10)
n.752_761del
c.269_278del (p.Val90GlufsTer10)
c.263_272del (p.Val88GlufsTer10)
7g.44152365T>ACA367402901GCKc.*267A>T (n.*267A>T)
c.269A>T (p.Lys90Met)
n.755A>T
c.272A>T (p.Lys91Met)
c.266A>T (p.Lys89Met)
7g.44152365T>CCA367402903GCKc.*267A>G (n.*267A>G)
c.269A>G (p.Lys90Arg)
n.755A>G
c.272A>G (p.Lys91Arg)
c.266A>G (p.Lys89Arg)
7g.44152365T>GCA367402900GCKc.*267A>C (n.*267A>C)
c.269A>C (p.Lys90Thr)
n.755A>C
c.272A>C (p.Lys91Thr)
c.266A>C (p.Lys89Thr)
ClinVar dbSNP
7g.44152366T>ACA367402908GCKc.*266A>T (n.*266A>T)
c.268A>T (p.Lys90Ter)
n.754A>T
c.271A>T (p.Lys91Ter)
c.265A>T (p.Lys89Ter)
7g.44152366T>CCA367402905GCKc.*266A>G (n.*266A>G)
c.268A>G (p.Lys90Glu)
n.754A>G
c.271A>G (p.Lys91Glu)
c.265A>G (p.Lys89Glu)
7g.44152366T>GCA367402906GCKc.*266A>C (n.*266A>C)
c.268A>C (p.Lys90Gln)
n.754A>C
c.271A>C (p.Lys91Gln)
c.265A>C (p.Lys89Gln)
7g.44152367C>ACA454610267GCKc.*265G>T (n.*265G>T)
c.267G>T (p.Val89=)
n.753G>T
c.270G>T (p.Val90=)
c.264G>T (p.Val88=)
COSMIC COSMIC COSMIC
7g.44152367C>GCA454610268GCKc.*265G>C (n.*265G>C)
c.267G>C (p.Val89=)
n.753G>C
c.270G>C (p.Val90=)
c.264G>C (p.Val88=)
7g.44152367C>TCA454610269GCKc.*265G>A (n.*265G>A)
c.267G>A (p.Val89=)
n.753G>A
c.270G>A (p.Val90=)
c.264G>A (p.Val88=)
gnomAD v4
7g.44152368A>CCA367402909GCKc.*264T>G (n.*264T>G)
c.266T>G (p.Val89Gly)
n.752T>G
c.269T>G (p.Val90Gly)
c.263T>G (p.Val88Gly)
7g.44152368A>GCA367402910GCKc.*264T>C (n.*264T>C)
c.266T>C (p.Val89Ala)
n.752T>C
c.269T>C (p.Val90Ala)
c.263T>C (p.Val88Ala)
7g.44152368A>TCA367402914GCKc.*264T>A (n.*264T>A)
c.266T>A (p.Val89Glu)
n.752T>A
c.269T>A (p.Val90Glu)
c.263T>A (p.Val88Glu)
7g.44152369C>ACA367402916GCKc.*263G>T (n.*263G>T)
c.265G>T (p.Val89Leu)
n.751G>T
c.268G>T (p.Val90Leu)
c.262G>T (p.Val88Leu)
7g.44152369C>GCA367402918GCKc.*263G>C (n.*263G>C)
c.265G>C (p.Val89Leu)
n.751G>C
c.268G>C (p.Val90Leu)
c.262G>C (p.Val88Leu)
7g.44152369C>TCA367402921GCKc.*263G>A (n.*263G>A)
c.265G>A (p.Val89Met)
n.751G>A
c.268G>A (p.Val90Met)
c.262G>A (p.Val88Met)
7g.44152370C>ACA454610270GCKc.*262G>T (n.*262G>T)
c.264G>T (p.Leu88=)
n.750G>T
c.267G>T (p.Leu89=)
c.261G>T (p.Leu87=)
gnomAD v4
7g.44152370C=CA1703637067GCKc.*262G= (n.*262G=)
c.264G= (p.Leu88=)
n.750G=
c.267G= (p.Leu89=)
c.261G= (p.Leu87=)
7g.44152370C>GCA454610271GCKc.*262G>C (n.*262G>C)
c.264G>C (p.Leu88=)
n.750G>C
c.267G>C (p.Leu89=)
c.261G>C (p.Leu87=)
7g.44152370C>TCA4239684GCKc.*262G>A (n.*262G>A)
c.264G>A (p.Leu88=)
n.750G>A
c.267G>A (p.Leu89=)
c.261G>A (p.Leu87=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.44152370_44152371insCATGCACAGATGTAACTGGCAGGCCACTTTGCTCA2682576254GCKc.*261_*262insAGCAAAGTGGCCTGCCAGTTACATCTGTGCATG (n.*261_*262insAGCAAAGTGGCCTGCCAGTTACATCTGTGCATG)
c.263_264insAGCAAAGTGGCCTGCCAGTTACATCTGTGCATG (p.Leu88_Val89insAlaLysTrpProAlaSerTyrIleCysAlaTrp)
n.749_750insAGCAAAGTGGCCTGCCAGTTACATCTGTGCATG
c.266_267insAGCAAAGTGGCCTGCCAGTTACATCTGTGCATG (p.Leu89_Val90insAlaLysTrpProAlaSerTyrIleCysAlaTrp)
c.260_261insAGCAAAGTGGCCTGCCAGTTACATCTGTGCATG (p.Leu87_Val88insAlaLysTrpProAlaSerTyrIleCysAlaTrp)
gnomAD v4
7g.44152371A>CCA367402924GCKc.*261T>G (n.*261T>G)
c.263T>G (p.Leu88Arg)
n.749T>G
c.266T>G (p.Leu89Arg)
c.260T>G (p.Leu87Arg)
7g.44152371A>GCA367402925GCKc.*261T>C (n.*261T>C)
c.263T>C (p.Leu88Pro)
n.749T>C
c.266T>C (p.Leu89Pro)
c.260T>C (p.Leu87Pro)
7g.44152371A>TCA367402927GCKc.*261T>A (n.*261T>A)
c.263T>A (p.Leu88Gln)
n.749T>A
c.266T>A (p.Leu89Gln)
c.260T>A (p.Leu87Gln)
7g.44152372G>ACA454610273GCKc.*260C>T (n.*260C>T)
c.262C>T (p.Leu88=)
n.748C>T
c.265C>T (p.Leu89=)
c.259C>T (p.Leu87=)
gnomAD v4
7g.44152372G>CCA367402931GCKc.*260C>G (n.*260C>G)
c.262C>G (p.Leu88Val)
n.748C>G
c.265C>G (p.Leu89Val)
c.259C>G (p.Leu87Val)
7g.44152372G>TCA367402929GCKc.*260C>A (n.*260C>A)
c.262C>A (p.Leu88Met)
n.748C>A
c.265C>A (p.Leu89Met)
c.259C>A (p.Leu87Met)
7g.44152373C>ACA367402934GCKc.*259G>T (n.*259G>T)
c.261G>T (p.Met87Ile)
n.747G>T
c.264G>T (p.Met88Ile)
c.258G>T (p.Met86Ile)
7g.44152373C>GCA367402936GCKc.*259G>C (n.*259G>C)
c.261G>C (p.Met87Ile)
n.747G>C
c.264G>C (p.Met88Ile)
c.258G>C (p.Met86Ile)
7g.44152373C>TCA367402937GCKc.*259G>A (n.*259G>A)
c.261G>A (p.Met87Ile)
n.747G>A
c.264G>A (p.Met88Ile)
c.258G>A (p.Met86Ile)
7g.44152374A>CCA367402939GCKc.*258T>G (n.*258T>G)
c.260T>G (p.Met87Arg)
n.746T>G
c.263T>G (p.Met88Arg)
c.257T>G (p.Met86Arg)
7g.44152374A>GCA367402942GCKc.*258T>C (n.*258T>C)
c.260T>C (p.Met87Thr)
n.746T>C
c.263T>C (p.Met88Thr)
c.257T>C (p.Met86Thr)
7g.44152374A>TCA367402944GCKc.*258T>A (n.*258T>A)
c.260T>A (p.Met87Lys)
n.746T>A
c.263T>A (p.Met88Lys)
c.257T>A (p.Met86Lys)
7g.44152375T>ACA367402945GCKc.*257A>T (n.*257A>T)
c.259A>T (p.Met87Leu)
n.745A>T
c.262A>T (p.Met88Leu)
c.256A>T (p.Met86Leu)
7g.44152375T>CCA367402947GCKc.*257A>G (n.*257A>G)
c.259A>G (p.Met87Val)
n.745A>G
c.262A>G (p.Met88Val)
c.256A>G (p.Met86Val)
7g.44152375T>GCA367402949GCKc.*257A>C (n.*257A>C)
c.259A>C (p.Met87Leu)
n.745A>C
c.262A>C (p.Met88Leu)
c.256A>C (p.Met86Leu)
7g.44152376C>ACA454610278GCKc.*256G>T (n.*256G>T)
c.258G>T (p.Val86=)
n.744G>T
c.261G>T (p.Val87=)
c.255G>T (p.Val85=)
7g.44152376C=CA1703637068GCKc.*256G= (n.*256G=)
c.258G= (p.Val86=)
n.744G=
c.261G= (p.Val87=)
c.255G= (p.Val85=)
7g.44152376C>GCA454610280GCKc.*256G>C (n.*256G>C)
c.258G>C (p.Val86=)
n.744G>C
c.261G>C (p.Val87=)
c.255G>C (p.Val85=)
7g.44152376C>TCA454610283GCKc.*256G>A (n.*256G>A)
c.258G>A (p.Val86=)
n.744G>A
c.261G>A (p.Val87=)
c.255G>A (p.Val85=)
dbSNP
7g.44152377A>CCA367402951GCKc.*255T>G (n.*255T>G)
c.257T>G (p.Val86Gly)
n.743T>G
c.260T>G (p.Val87Gly)
c.254T>G (p.Val85Gly)
7g.44152377A>GCA367402952GCKc.*255T>C (n.*255T>C)
c.257T>C (p.Val86Ala)
n.743T>C
c.260T>C (p.Val87Ala)
c.254T>C (p.Val85Ala)
7g.44152377A>TCA367402953GCKc.*255T>A (n.*255T>A)
c.257T>A (p.Val86Glu)
n.743T>A
c.260T>A (p.Val87Glu)
c.254T>A (p.Val85Glu)
7g.44152378C>ACA367402955GCKc.*254G>T (n.*254G>T)
c.256G>T (p.Val86Leu)
n.742G>T
c.259G>T (p.Val87Leu)
c.253G>T (p.Val85Leu)
gnomAD v4
7g.44152378C>GCA367402957GCKc.*254G>C (n.*254G>C)
c.256G>C (p.Val86Leu)
n.742G>C
c.259G>C (p.Val87Leu)
c.253G>C (p.Val85Leu)
7g.44152378C>TCA367402954GCKc.*254G>A (n.*254G>A)
c.256G>A (p.Val86Met)
n.742G>A
c.259G>A (p.Val87Met)
c.253G>A (p.Val85Met)
7g.44152379_44152380delCA2580077163GCKc.*253_*254del (n.*253_*254del)
c.255_256del (p.Arg85SerfsTer10)
n.741_742del
c.258_259del (p.Arg86SerfsTer10)
c.252_253del (p.Arg84SerfsTer10)
ClinVar
7g.44152379C>ACA367402958GCKc.*253G>T (n.*253G>T)
c.255G>T (p.Arg85Ser)
n.741G>T
c.258G>T (p.Arg86Ser)
c.252G>T (p.Arg84Ser)
ClinVar dbSNP

Number of alleles fetched