Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129530897_129530906delCA2577961749RHOc.383_392del (p.Leu128TrpfsTer13)
gnomAD v4
3g.129530892G>ACA354497924RHOc.378G>A (p.Trp126Ter)
3g.129530892G>CCA354497925RHOc.378G>C (p.Trp126Cys)
3g.129530892G>TCA354497927RHOc.378G>T (p.Trp126Cys)
3g.129530893T>ACA354497932RHOc.379T>A (p.Ser127Thr)
3g.129530893T>CCA354497930RHOc.379T>C (p.Ser127Pro)
3g.129530893T>GCA354497928RHOc.379T>G (p.Ser127Ala)
3g.129530894C>ACA354497935RHOc.380C>A (p.Ser127Tyr)
ClinVar
3g.129530894C>GCA354497936RHOc.380C>G (p.Ser127Cys)
3g.129530894C>TCA354497937RHOc.380C>T (p.Ser127Phe)
ClinVar dbSNP
3g.129530894_129530896delinsCCTCA1401209216RHOc.380_382delinsCCT (p.Ser127=)
3g.129530895C>ACA435643723RHOc.381C>A (p.Ser127=)
3g.129530895C=CA1401209225RHOc.381C= (p.Ser127=)
3g.129530895C>GCA2607148RHOc.381C>G (p.Ser127=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129530895C>TCA2607149RHOc.381C>T (p.Ser127=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129530895_129530896delCA2607147RHOc.381_382del (p.Leu128GlyfsTer13)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129530896T>ACA354497941RHOc.382T>A (p.Leu128Met)
3g.129530896T>CCA435643726RHOc.382T>C (p.Leu128=)
3g.129530896T>GCA354497944RHOc.382T>G (p.Leu128Val)
3g.129530896_129530899delinsTTGGCA1401209234RHOc.382_385delinsTTGG (p.Leu128=)
3g.129530897T>ACA354497945RHOc.383T>A (p.Leu128Ter)
3g.129530897T>CCA354497948RHOc.383T>C (p.Leu128Ser)
3g.129530897T>GCA354497950RHOc.383T>G (p.Leu128Trp)
3g.129530901_129530903delCA1401209238RHOc.387_389del (p.Val130del)
dbSNP
3g.129530898G>ACA435643729RHOc.384G>A (p.Leu128=)
3g.129530898G>CCA354497954RHOc.384G>C (p.Leu128Phe)
3g.129530898G>TCA354497957RHOc.384G>T (p.Leu128Phe)
3g.129530899G>ACA354497965RHOc.385G>A (p.Val129Met)
3g.129530899G>CCA354497967RHOc.385G>C (p.Val129Leu)
3g.129530899G>TCA354497963RHOc.385G>T (p.Val129Leu)
3g.129530900T>ACA354497971RHOc.386T>A (p.Val129Glu)
3g.129530900T>CCA354497972RHOc.386T>C (p.Val129Ala)
3g.129530900T>GCA354497974RHOc.386T>G (p.Val129Gly)
3g.129530901G>ACA435643734RHOc.387G>A (p.Val129=)
3g.129530901G>CCA435643735RHOc.387G>C (p.Val129=)
3g.129530901G>TCA435643736RHOc.387G>T (p.Val129=)
3g.129530902G>ACA354497976RHOc.388G>A (p.Val130Ile)
3g.129530902G>CCA354497979RHOc.388G>C (p.Val130Leu)
3g.129530902G>TCA354497981RHOc.388G>T (p.Val130Phe)
3g.129530903T>ACA354497983RHOc.389T>A (p.Val130Asp)
3g.129530903T>CCA354497984RHOc.389T>C (p.Val130Ala)
3g.129530903T>GCA354497985RHOc.389T>G (p.Val130Gly)
3g.129530904C>ACA435643742RHOc.390C>A (p.Val130=)
3g.129530904C=CA1401209242RHOc.390C= (p.Val130=)
3g.129530904C>GCA435643743RHOc.390C>G (p.Val130=)
3g.129530904C>TCA435643744RHOc.390C>T (p.Val130=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129530905C>ACA354497988RHOc.391C>A (p.Leu131Met)
3g.129530905C>GCA354497992RHOc.391C>G (p.Leu131Val)
3g.129530905C>TCA435643745RHOc.391C>T (p.Leu131=)
3g.129530906T>ACA354498000RHOc.392T>A (p.Leu131Gln)

Number of alleles fetched