Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129530962delCA645514953RHOc.448del (p.Glu150ArgfsTer?)
COSMIC
3g.129530962G>ACA122824RHOc.448G>A (p.Glu150Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129530962G>CCA2607161RHOc.448G>C (p.Glu150Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129530962G=CA1401209417RHOc.448G= (p.Glu150=)
3g.129530962G>TCA354498282RHOc.448G>T (p.Glu150Ter)
3g.129530963A>CCA354498284RHOc.449A>C (p.Glu150Ala)
3g.129530963A>GCA354498286RHOc.449A>G (p.Glu150Gly)
3g.129530963A>TCA354498290RHOc.449A>T (p.Glu150Val)
3g.129530964G>ACA435643952RHOc.450G>A (p.Glu150=)
3g.129530964G>CCA354498294RHOc.450G>C (p.Glu150Asp)
dbSNP gnomAD v4
3g.129530964G=CA1401209423RHOc.450G= (p.Glu150=)
3g.129530964G>TCA354498295RHOc.450G>T (p.Glu150Asp)
3g.129530965A>CCA354498296RHOc.451A>C (p.Asn151His)
3g.129530965A>GCA354498301RHOc.451A>G (p.Asn151Asp)
3g.129530965A>TCA354498298RHOc.451A>T (p.Asn151Tyr)
3g.129530966A=CA1401209428RHOc.452A= (p.Asn151=)
3g.129530966A>CCA354498304RHOc.452A>C (p.Asn151Thr)
3g.129530966A>GCA354498309RHOc.452A>G (p.Asn151Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129530966A>TCA354498306RHOc.452A>T (p.Asn151Ile)
3g.129530967C>ACA354498312RHOc.453C>A (p.Asn151Lys)
3g.129530967C>GCA354498315RHOc.453C>G (p.Asn151Lys)
3g.129530967C>TCA435643964RHOc.453C>T (p.Asn151=)
dbSNP gnomAD v4
3g.129530968C>ACA354498318RHOc.454C>A (p.His152Asn)
3g.129530968C=CA1401209432RHOc.454C= (p.His152=)
3g.129530968C>GCA354498321RHOc.454C>G (p.His152Asp)
3g.129530968C>TCA354498322RHOc.454C>T (p.His152Tyr)
dbSNP gnomAD v2 gnomAD v4
3g.129530969A>CCA354498324RHOc.455A>C (p.His152Pro)
3g.129530969A>GCA354498330RHOc.455A>G (p.His152Arg)
gnomAD v4
3g.129530969A>TCA354498336RHOc.455A>T (p.His152Leu)
3g.129530970T>ACA354498340RHOc.456T>A (p.His152Gln)
3g.129530970T>CCA435643976RHOc.456T>C (p.His152=)
dbSNP gnomAD v4
3g.129530970T>GCA354498344RHOc.456T>G (p.His152Gln)
gnomAD v4
3g.129530971G>ACA354498352RHOc.457G>A (p.Ala153Thr)
dbSNP gnomAD v2
3g.129530971G>CCA354498357RHOc.457G>C (p.Ala153Pro)
3g.129530971G=CA1401209436RHOc.457G= (p.Ala153=)
3g.129530971G>TCA354498359RHOc.457G>T (p.Ala153Ser)
3g.129530972C>ACA354498362RHOc.458C>A (p.Ala153Asp)
ClinVar dbSNP
3g.129530972C=CA1401209444RHOc.458C= (p.Ala153=)
3g.129530972C>GCA354498365RHOc.458C>G (p.Ala153Gly)
COSMIC
3g.129530972C>TCA354498363RHOc.458C>T (p.Ala153Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.129530973C>ACA435643986RHOc.459C>A (p.Ala153=)
gnomAD v4
3g.129530973C=CA1401209449RHOc.459C= (p.Ala153=)
3g.129530973C>GCA435643988RHOc.459C>G (p.Ala153=)
dbSNP gnomAD v2 gnomAD v4
3g.129530973C>TCA435643990RHOc.459C>T (p.Ala153=)
dbSNP
3g.129530974A>CCA354498366RHOc.460A>C (p.Ile154Leu)
3g.129530974A>GCA354498368RHOc.460A>G (p.Ile154Val)
gnomAD v4
3g.129530974A>TCA354498370RHOc.460A>T (p.Ile154Phe)
3g.129530975T>ACA354498371RHOc.461T>A (p.Ile154Asn)
3g.129530975T>CCA354498373RHOc.461T>C (p.Ile154Thr)
3g.129530975T>GCA354498375RHOc.461T>G (p.Ile154Ser)

Number of alleles fetched