Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532268_129532358dupCA915941573RHOc.548_638dup (p.Ile214AlafsTer?)
ClinVar dbSNP
3g.129532282G>ACA270025RHOc.562G>A (p.Gly188Arg)
ClinVar dbSNP COSMIC
3g.129532282G>CCA354499264RHOc.562G>C (p.Gly188Arg)
3g.129532282G=CA1401211010RHOc.562G= (p.Gly188=)
3g.129532282G>TCA354499268RHOc.562G>T (p.Gly188Ter)
3g.129532283G>ACA354499271RHOc.563G>A (p.Gly188Glu)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129532283G>CCA354499274RHOc.563G>C (p.Gly188Ala)
3g.129532283G=CA1401211016RHOc.563G= (p.Gly188=)
3g.129532283G>TCA354499278RHOc.563G>T (p.Gly188Val)
3g.129532284A>CCA435644717RHOc.564A>C (p.Gly188=)
3g.129532284A>GCA435644719RHOc.564A>G (p.Gly188=)
3g.129532284A>TCA435644722RHOc.564A>T (p.Gly188=)
3g.129532285A>CCA354499281RHOc.565A>C (p.Ile189Leu)
3g.129532285A>GCA354499284RHOc.565A>G (p.Ile189Val)
3g.129532285A>TCA354499286RHOc.565A>T (p.Ile189Phe)
3g.129532286T>ACA354499293RHOc.566T>A (p.Ile189Asn)
3g.129532286T>CCA354499289RHOc.566T>C (p.Ile189Thr)
3g.129532286T>GCA354499291RHOc.566T>G (p.Ile189Ser)
3g.129532287C>ACA435644739RHOc.567C>A (p.Ile189=)
3g.129532287C=CA1401211019RHOc.567C= (p.Ile189=)
3g.129532287C>GCA354499296RHOc.567C>G (p.Ile189Met)
3g.129532287C>TCA2607208RHOc.567C>T (p.Ile189=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532288G>ACA256670RHOc.568G>A (p.Asp190Asn)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.129532288G>CCA354499304RHOc.568G>C (p.Asp190His)
ClinVar dbSNP
3g.129532288G=CA1401211029RHOc.568G= (p.Asp190=)
3g.129532288G>TCA256684RHOc.568G>T (p.Asp190Tyr)
ClinVar dbSNP gnomAD v4
3g.129532289A=CA1401211041RHOc.569A= (p.Asp190=)
3g.129532289A>CCA354499308RHOc.569A>C (p.Asp190Ala)
3g.129532289A>GCA256673RHOc.569A>G (p.Asp190Gly)
ClinVar dbSNP
3g.129532289A>TCA354499312RHOc.569A>T (p.Asp190Val)
3g.129532290C>ACA354499314RHOc.570C>A (p.Asp190Glu)
3g.129532290C=CA1401211050RHOc.570C= (p.Asp190=)
3g.129532290C>GCA354499320RHOc.570C>G (p.Asp190Glu)
ClinVar dbSNP
3g.129532290C>TCA435644762RHOc.570C>T (p.Asp190=)
3g.129532291T>ACA354499324RHOc.571T>A (p.Tyr191Asn)
ClinVar dbSNP
3g.129532291T>CCA354499328RHOc.571T>C (p.Tyr191His)
3g.129532291T>GCA354499331RHOc.571T>G (p.Tyr191Asp)
ClinVar dbSNP
3g.129532291T=CA1401211059RHOc.571T= (p.Tyr191=)
3g.129532292A>CCA354469676RHOc.572A>C (p.Tyr191Ser)
3g.129532292A>GCA354469678RHOc.572A>G (p.Tyr191Cys)
3g.129532292A>TCA354469675RHOc.572A>T (p.Tyr191Phe)
gnomAD v4
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)

Number of alleles fetched