Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532268_129532358dupCA915941573RHOc.548_638dup (p.Ile214AlafsTer?)
ClinVar dbSNP
3g.129532293C>ACA354469680RHOc.573C>A (p.Tyr191Ter)
3g.129532293C>GCA354469682RHOc.573C>G (p.Tyr191Ter)
3g.129532293C>TCA435768906RHOc.573C>T (p.Tyr191=)
COSMIC
3g.129532294T>ACA354469683RHOc.574T>A (p.Tyr192Asn)
gnomAD v4
3g.129532294T>CCA354469684RHOc.574T>C (p.Tyr192His)
3g.129532294T>GCA354469685RHOc.574T>G (p.Tyr192Asp)
3g.129532294dupCA2577961791RHOc.574dup (p.Tyr192LeufsTer?)
gnomAD v4
3g.129532295A=CA1401211071RHOc.575A= (p.Tyr192=)
3g.129532295A>CCA354469686RHOc.575A>C (p.Tyr192Ser)
3g.129532295A>GCA354469688RHOc.575A>G (p.Tyr192Cys)
dbSNP gnomAD v3 gnomAD v4
3g.129532295A>TCA354469690RHOc.575A>T (p.Tyr192Phe)
3g.129532296C>ACA354469691RHOc.576C>A (p.Tyr192Ter)
3g.129532296C=CA1401211074RHOc.576C= (p.Tyr192=)
3g.129532296C>GCA354469693RHOc.576C>G (p.Tyr192Ter)
3g.129532296C>TCA82620436RHOc.576C>T (p.Tyr192=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532297A>CCA354469696RHOc.577A>C (p.Thr193Pro)
3g.129532297A>GCA354469697RHOc.577A>G (p.Thr193Ala)
3g.129532297A>TCA354469698RHOc.577A>T (p.Thr193Ser)
3g.129532298C>ACA2607210RHOc.578C>A (p.Thr193Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532298C=CA1401211083RHOc.578C= (p.Thr193=)
3g.129532298C>GCA354469702RHOc.578C>G (p.Thr193Arg)
3g.129532298C>TCA2607209RHOc.578C>T (p.Thr193Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532299G>ACA2607211RHOc.579G>A (p.Thr193=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532299G>CCA82620446RHOc.579G>C (p.Thr193=)
dbSNP gnomAD v3 gnomAD v4
3g.129532299G=CA1401211090RHOc.579G= (p.Thr193=)
3g.129532299G>TCA435768913RHOc.579G>T (p.Thr193=)
gnomAD v4
3g.129532300C>ACA354469705RHOc.580C>A (p.Leu194Ile)
3g.129532300C>GCA354469707RHOc.580C>G (p.Leu194Val)
3g.129532300C>TCA354469709RHOc.580C>T (p.Leu194Phe)
3g.129532301T>ACA354469711RHOc.581T>A (p.Leu194His)
3g.129532301T>CCA354469712RHOc.581T>C (p.Leu194Pro)
3g.129532301T>GCA354469714RHOc.581T>G (p.Leu194Arg)
3g.129532302C>ACA435768918RHOc.582C>A (p.Leu194=)
3g.129532302C=CA1401211094RHOc.582C= (p.Leu194=)
3g.129532302C>GCA435768920RHOc.582C>G (p.Leu194=)
dbSNP gnomAD v2 gnomAD v4
3g.129532302C>TCA435768921RHOc.582C>T (p.Leu194=)
gnomAD v4
3g.129532303A>CCA354469715RHOc.583A>C (p.Lys195Gln)
3g.129532303A>GCA354469717RHOc.583A>G (p.Lys195Glu)
3g.129532303A>TCA354469719RHOc.583A>T (p.Lys195Ter)
3g.129532304A>CCA354469720RHOc.584A>C (p.Lys195Thr)
3g.129532304A>GCA354469722RHOc.584A>G (p.Lys195Arg)
3g.129532304A>TCA354469724RHOc.584A>T (p.Lys195Met)
3g.129532305G>ACA435768926RHOc.585G>A (p.Lys195=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129532305G>CCA354469727RHOc.585G>C (p.Lys195Asn)
3g.129532305G=CA1401211097RHOc.585G= (p.Lys195=)
3g.129532305G>TCA354469726RHOc.585G>T (p.Lys195Asn)
dbSNP
3g.129532306C>ACA10615276RHOc.586C>A (p.Pro196Thr)
ClinVar dbSNP gnomAD v4
3g.129532306C=CA1401211103RHOc.586C= (p.Pro196=)
3g.129532306C>GCA354469730RHOc.586C>G (p.Pro196Ala)

Number of alleles fetched