Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.179203764_179203765insCGTAAATATTCTTTGTGCAACCTACGTGAACA2580611970PIK3CAc.1034_1035insCGTAAATATTCTTTGTGCAACCTACGTGAA (p.Asn345_Val346insValAsnIleLeuCysAlaThrTyrValAsn)
n.788_789insCGTAAATATTCTTTGTGCAACCTACGTGAA
n.3841_3842insCGTAAATATTCTTTGTGCAACCTACGTGAA
3g.179203746_179203775dupCA2580611922PIK3CAc.1016_1045dup (p.Ile348_Arg349insLeuCysAlaThrTyrValAsnValAsnIle)
n.770_799dup
n.3823_3852dup
3g.179203763A=CA1423665597PIK3CAc.1033A= (p.Asn345=)
n.787A=
n.3840A=
3g.179203763A>CCA16602924PIK3CAc.1033A>C (p.Asn345His)
n.787A>C
n.3840A>C
ClinVar dbSNP COSMIC COSMIC
3g.179203763A>GCA355281447PIK3CAc.1033A>G (p.Asn345Asp)
n.787A>G
n.3840A>G
dbSNP
3g.179203763A>TCA355281448PIK3CAc.1033A>T (p.Asn345Tyr)
n.787A>T
n.3840A>T
dbSNP
3g.179203764A=CA1423665612PIK3CAc.1034A= (p.Asn345=)
n.788A=
n.3841A=
3g.179203764A>CCA16602923PIK3CAc.1034A>C (p.Asn345Thr)
n.788A>C
n.3841A>C
ClinVar dbSNP COSMIC COSMIC
3g.179203764A>GCA355281458PIK3CAc.1034A>G (p.Asn345Ser)
n.788A>G
n.3841A>G
ClinVar dbSNP COSMIC
3g.179203764A>TCA16602922PIK3CAc.1034A>T (p.Asn345Ile)
n.788A>T
n.3841A>T
ClinVar dbSNP COSMIC COSMIC
3g.179203765T>ACA16602517PIK3CAc.1035T>A (p.Asn345Lys)
n.789T>A
n.3842T>A
ClinVar dbSNP COSMIC COSMIC
3g.179203765T>CCA437316057PIK3CAc.1035T>C (p.Asn345=)
n.789T>C
n.3842T>C
dbSNP gnomAD v4
3g.179203765T>GCA16602518PIK3CAc.1035T>G (p.Asn345Lys)
n.789T>G
n.3842T>G
ClinVar dbSNP
3g.179203765T=CA1423665626PIK3CAc.1035T= (p.Asn345=)
n.789T=
n.3842T=
3g.179203766G>ACA355281473PIK3CAc.1036G>A (p.Val346Ile)
n.790G>A
n.3843G>A
dbSNP
3g.179203766G>CCA88560757PIK3CAc.1036G>C (p.Val346Leu)
n.790G>C
n.3843G>C
dbSNP
3g.179203766G=CA1423665638PIK3CAc.1036G= (p.Val346=)
n.790G=
n.3843G=
3g.179203766G>TCA355281475PIK3CAc.1036G>T (p.Val346Leu)
n.790G>T
n.3843G>T
3g.179203767T>ACA355281476PIK3CAc.1037T>A (p.Val346Glu)
n.791T>A
n.3844T>A
3g.179203767T>CCA355281477PIK3CAc.1037T>C (p.Val346Ala)
n.791T>C
n.3844T>C
3g.179203767T>GCA355281479PIK3CAc.1037T>G (p.Val346Gly)
n.791T>G
n.3844T>G
COSMIC COSMIC
3g.179203768A>CCA437316058PIK3CAc.1038A>C (p.Val346=)
n.792A>C
n.3845A>C
3g.179203768A>GCA437316059PIK3CAc.1038A>G (p.Val346=)
n.792A>G
n.3845A>G
3g.179203768A>TCA437316060PIK3CAc.1038A>T (p.Val346=)
n.792A>T
n.3845A>T
dbSNP
3g.179203769A>CCA355281481PIK3CAc.1039A>C (p.Asn347His)
n.793A>C
n.3846A>C
3g.179203769A>GCA355281483PIK3CAc.1039A>G (p.Asn347Asp)
n.793A>G
n.3846A>G
3g.179203769A>TCA355281482PIK3CAc.1039A>T (p.Asn347Tyr)
n.793A>T
n.3846A>T
3g.179203770A=CA1423665645PIK3CAc.1040A= (p.Asn347=)
n.794A=
n.3847A=
3g.179203770A>CCA355281484PIK3CAc.1040A>C (p.Asn347Thr)
n.794A>C
n.3847A>C
3g.179203770A>GCA355281487PIK3CAc.1040A>G (p.Asn347Ser)
n.794A>G
n.3847A>G
dbSNP
3g.179203770A>TCA2710619PIK3CAc.1040A>T (p.Asn347Ile)
n.794A>T
n.3847A>T
dbSNP ExAC gnomAD v2 gnomAD v4
3g.179203771T>ACA355281500PIK3CAc.1041T>A (p.Asn347Lys)
n.795T>A
n.3848T>A
dbSNP
3g.179203771T>CCA437316061PIK3CAc.1041T>C (p.Asn347=)
n.795T>C
n.3848T>C
dbSNP
3g.179203771T>GCA355281505PIK3CAc.1041T>G (p.Asn347Lys)
n.795T>G
n.3848T>G
COSMIC
3g.179203772A>CCA355281512PIK3CAc.1042A>C (p.Ile348Leu)
n.796A>C
n.3849A>C
3g.179203772A>GCA355281519PIK3CAc.1042A>G (p.Ile348Val)
n.796A>G
n.3849A>G
dbSNP
3g.179203772A>TCA355281537PIK3CAc.1042A>T (p.Ile348Phe)
n.796A>T
n.3849A>T
dbSNP COSMIC
3g.179203773T>ACA355281539PIK3CAc.1043T>A (p.Ile348Asn)
n.797T>A
n.3850T>A
dbSNP
3g.179203773T>CCA355281541PIK3CAc.1043T>C (p.Ile348Thr)
n.797T>C
n.3850T>C
ClinVar
3g.179203773T>GCA355281543PIK3CAc.1043T>G (p.Ile348Ser)
n.797T>G
n.3850T>G
gnomAD v4
3g.179203774T>ACA437316062PIK3CAc.1044T>A (p.Ile348=)
n.798T>A
n.3851T>A
3g.179203774T>CCA437316063PIK3CAc.1044T>C (p.Ile348=)
n.798T>C
n.3851T>C
3g.179203774T>GCA355281549PIK3CAc.1044T>G (p.Ile348Met)
n.798T>G
n.3851T>G
3g.179203775C>ACA2710620PIK3CAc.1045C>A (p.Arg349=)
n.799C>A
n.3852C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.179203775C=CA1423665650PIK3CAc.1045C= (p.Arg349=)
n.799C=
n.3852C=
3g.179203775C>GCA355281573PIK3CAc.1045C>G (p.Arg349Gly)
n.799C>G
n.3852C>G
3g.179203775C>TCA355281567PIK3CAc.1045C>T (p.Arg349Ter)
n.799C>T
n.3852C>T
dbSNP gnomAD v4 COSMIC
3g.179203776G>ACA355281580PIK3CAc.1046G>A (p.Arg349Gln)
n.800G>A
n.3853G>A
dbSNP gnomAD v4
3g.179203776G>CCA355281581PIK3CAc.1046G>C (p.Arg349Pro)
n.800G>C
n.3853G>C
dbSNP
3g.179203776G>TCA355281583PIK3CAc.1046G>T (p.Arg349Leu)
n.800G>T
n.3853G>T
dbSNP gnomAD v4

Number of alleles fetched