Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.172448249_172448270delCA2524707107GHSRc.144_165del (p.Thr49TrpfsTer?)
3g.172448266A>CCA355516450GHSRc.148T>G (p.Cys50Gly)
3g.172448266A>GCA355516446GHSRc.148T>C (p.Cys50Arg)
3g.172448266A>TCA355516448GHSRc.148T>A (p.Cys50Ser)
3g.172448267G>ACA436965603GHSRc.147C>T (p.Thr49=)
gnomAD v4
3g.172448267G>CCA436965605GHSRc.147C>G (p.Thr49=)
3g.172448267G>TCA436965607GHSRc.147C>A (p.Thr49=)
3g.172448268G>ACA2706523GHSRc.146C>T (p.Thr49Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.172448268G>CCA355516453GHSRc.146C>G (p.Thr49Ser)
3g.172448268G=CA1420511857GHSRc.146C= (p.Thr49=)
3g.172448268G>TCA355516455GHSRc.146C>A (p.Thr49Asn)
dbSNP gnomAD v2 gnomAD v4
3g.172448269T>ACA355516457GHSRc.145A>T (p.Thr49Ser)
3g.172448269T>CCA355516458GHSRc.145A>G (p.Thr49Ala)
3g.172448269T>GCA355516459GHSRc.145A>C (p.Thr49Pro)
3g.172448270G>ACA2706524GHSRc.144C>T (p.Ala48=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.172448270G>CCA436965610GHSRc.144C>G (p.Ala48=)
3g.172448270G=CA1420511858GHSRc.144C= (p.Ala48=)
3g.172448270G>TCA436965611GHSRc.144C>A (p.Ala48=)
3g.172448270_172448283delCA645535948GHSRc.131_144del (p.Ala44AspfsTer?)
COSMIC COSMIC
3g.172448271G>ACA355516469GHSRc.143C>T (p.Ala48Val)
3g.172448271G>CCA355516464GHSRc.143C>G (p.Ala48Gly)
3g.172448271G=CA1420511859GHSRc.143C= (p.Ala48=)
3g.172448271G>TCA355516466GHSRc.143C>A (p.Ala48Asp)
dbSNP gnomAD v3 gnomAD v4
3g.172448272C>ACA355516471GHSRc.142G>T (p.Ala48Ser)
3g.172448272C>GCA355516473GHSRc.142G>C (p.Ala48Pro)
3g.172448272C>TCA355516474GHSRc.142G>A (p.Ala48Thr)
3g.172448273T>ACA436965613GHSRc.141A>T (p.Thr47=)
3g.172448273T>CCA436965615GHSRc.141A>G (p.Thr47=)
3g.172448273T>GCA436965617GHSRc.141A>C (p.Thr47=)
3g.172448273_172448274insAGGGTGACTTCATATGAGATTGTTTGGGCTACTGCTCGCATCA2668560153GHSRc.141_142insTGCGAGCAGTAGCCCAAACAATCTCATATGAAGTCACCCTA (p.Ala48CysfsTer4)
gnomAD v4
3g.172448274G>ACA355516480GHSRc.140C>T (p.Thr47Ile)
3g.172448274G>CCA355516478GHSRc.140C>G (p.Thr47Arg)
3g.172448274G>TCA355516476GHSRc.140C>A (p.Thr47Lys)
gnomAD v4
3g.172448274_172448279delCA2541600003GHSRc.135_140del (p.Val46_Thr47del)
3g.172448275T>ACA355516483GHSRc.139A>T (p.Thr47Ser)
3g.172448275T>CCA355516485GHSRc.139A>G (p.Thr47Ala)
3g.172448275T>GCA355516487GHSRc.139A>C (p.Thr47Pro)
3g.172448276G>ACA436965619GHSRc.138C>T (p.Val46=)
dbSNP
3g.172448276G>CCA436965621GHSRc.138C>G (p.Val46=)
3g.172448276G=CA1420511860GHSRc.138C= (p.Val46=)
3g.172448276G>TCA436965623GHSRc.138C>A (p.Val46=)
3g.172448277A=CA1420511861GHSRc.137T= (p.Val46=)
3g.172448277A>CCA355516489GHSRc.137T>G (p.Val46Gly)
3g.172448277A>GCA355516492GHSRc.137T>C (p.Val46Ala)
gnomAD v4
3g.172448277A>TCA2706525GHSRc.137T>A (p.Val46Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.172448278C>ACA355516495GHSRc.136G>T (p.Val46Phe)
dbSNP gnomAD v4
3g.172448278C=CA1420511862GHSRc.136G= (p.Val46=)
3g.172448278C>GCA2706526GHSRc.136G>C (p.Val46Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.172448278C>TCA355516497GHSRc.136G>A (p.Val46Ile)
3g.172448279G>ACA436965627GHSRc.135C>T (p.Gly45=)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched